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dusp16  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc dusp16
    FBXL18 targeted <t>DUSP16</t> as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001
    Dusp16, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dusp16/DUSP16%2FMKP7+Rabbit+mAb/pmc12085810-91-9-11
    Average 90 stars, based on 8 article reviews
    dusp16 - by Bioz Stars, 2026-09
    90/100 stars

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    1) Product Images from "FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway"

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    Journal: Cancer Cell International

    doi: 10.1186/s12935-025-03808-9

    FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001
    Figure Legend Snippet: FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001

    Techniques Used: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Western Blot, Quantitative RT-PCR, Control, Comparison, Stable Transfection, Knockdown, Immunoprecipitation

    FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001
    Figure Legend Snippet: FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001

    Techniques Used: Activation Assay, Western Blot, Transfection, Plasmid Preparation

    Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001
    Figure Legend Snippet: Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001

    Techniques Used: In Vivo, Western Blot, Quantitative RT-PCR

    Related Articles

    Ubiquitin Proteomics:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Co-Immunoprecipitation Assay:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Western Blot:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Quantitative RT-PCR:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Control:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Comparison:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Stable Transfection:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Knockdown:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Immunoprecipitation:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Activation Assay:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Transfection:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Plasmid Preparation:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    In Vivo:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Negative Control:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Knock-Out:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Expressing:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Transduction:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Over Expression:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.

    Cell Culture:

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.The next day, the resultant mixtures were incubated with the pre-treated protein A + G agarose beads (CST, USA) at 4 °C with gently rotation for 2 h. After centrifuging at 2000 rpm for 5 min, the supernatant was discarded and the precipitates were collected for subsequent western blot analysis.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).. For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.For the in vivo ubiquitination assay, cells were of different groups were treated with MG132 (20 µM; MCE, USA) for 6 h before collection.

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway
    Article Snippet: GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.GAPDH protein level was employed for normalization, and the relative protein expression level was determined by ImageJ software.. The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004-100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

    Article Title: MAP3K1 and MAP2K4 mutations are associated with sensitivity to MEK inhibitors in multiple cancer models
    Article Snippet: Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.Selumetinib (S1008), trametinib (S2673), SCH772984 (S7101), JNK-IN-8 (S4901) and dacomitinib (S2727) were purchased from Selleck Chemicals.. Antibodies against p-JNK (T183/Y185) (4668), JNK (9252), p-JUN (S63) (2361), JUN (2315), MAP2K4 (9152), DUSP4 (5149), DUSP16 (5523), p-ERBB2 (Y1221/1222) (2243), ERBB2 (4290), p-ERBB3 (Y1222) (4784), ERBB3 (4754), p-ERBB4 (Y1284) (4757) and ERBB4 (4795) were purchased from Cell Signaling Technology.. Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.Antibodies against p-ERK (E-4), ERK1 (C-16), ERK2 (C-14) and HSP90 (H-114) were purchased from Santa Cruz Biotechnology.



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    Image Search Results


    FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).

    Techniques: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Western Blot, Quantitative RT-PCR, Control, Comparison, Stable Transfection, Knockdown, Immunoprecipitation

    FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).

    Techniques: Activation Assay, Western Blot, Transfection, Plasmid Preparation

    Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA), DUSP16 (#5523, CST, USA), FLAG (#14793, CST, USA), HA (#3724, CST, USA).

    Techniques: In Vivo, Western Blot, Quantitative RT-PCR

    Fig. 5 FBXL18 targeted DUSP16 as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001

    Journal: Cancer cell international

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: Fig. 5 FBXL18 targeted DUSP16 as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001

    Article Snippet: SiRNA specifically targeting DUSP16 or negative control siRNA (siNeg) were obtained from Sangon Biotech (Shanghai, China).

    Techniques: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Western Blot, Quantitative RT-PCR, Control, Comparison, Stable Transfection, Knockdown, Immunoprecipitation

    Fig. 7 Silence of FBXL18 inhibited EC growth in vivo. (A) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. (B) Representative images of xenograft tumors in shNC and shFBXL18 groups. (C) Tumor weights of shNC and shFBXL18 groups were measured at the end point. (E) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. (F) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. *P < 0.05; **P < 0.01; ***P < 0.001

    Journal: Cancer cell international

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: Fig. 7 Silence of FBXL18 inhibited EC growth in vivo. (A) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. (B) Representative images of xenograft tumors in shNC and shFBXL18 groups. (C) Tumor weights of shNC and shFBXL18 groups were measured at the end point. (E) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. (F) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. *P < 0.05; **P < 0.01; ***P < 0.001

    Article Snippet: SiRNA specifically targeting DUSP16 or negative control siRNA (siNeg) were obtained from Sangon Biotech (Shanghai, China).

    Techniques: In Vivo, Western Blot, Quantitative RT-PCR

    FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: FBXL18 targeted DUSP16 as a ubiquitination substrate. ( A-B ) The results of Co-IP and western blotting assays revealed the endogenous and exogenous interaction of FBXL18 and DUSP16. ( C-D ) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. ( E-F ) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. ( G-H ) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. ( I-J ) DUSP16 protein half-life in EC cells of LV-Control and LV-FBXL18 groups were evaluated by CHX chase assay. ( K-L ) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. ( M-N ) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: SiRNA specifically targeting DUSP16 or negative control siRNA (siNeg) were obtained from Sangon Biotech (Shanghai, China).

    Techniques: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Western Blot, Quantitative RT-PCR, Control, Comparison, Stable Transfection, Knockdown, Immunoprecipitation

    FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: FBXL18 promoted EC cell malignancy via DUSP16-mediated activation of JNK signaling. ( A-C ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells of siNeg and siDUSP16 groups, and quantitative analysis. ( D-F ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells after overexpressing DUSP16, and quantitative analysis. ( G-I ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with LV-Ctrl + Vector, LV-Ctrl + DUSP16, LV-FBXL18 + Vector, LV-FBXL18 + DUSP16, and quantitative analysis. ( J-L ) Western blot analysis of DUSP16, JNK, p-JNK, c-JUN, and p-c-JUN levels in EC cells transfected with shNC + siNeg, shNC + siDUSP16, shFBXL18 + siNeg, shFBXL18 + siDUSP16, and quantitative analysis. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: SiRNA specifically targeting DUSP16 or negative control siRNA (siNeg) were obtained from Sangon Biotech (Shanghai, China).

    Techniques: Activation Assay, Western Blot, Transfection, Plasmid Preparation

    Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cancer Cell International

    Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway

    doi: 10.1186/s12935-025-03808-9

    Figure Lengend Snippet: Silence of FBXL18 inhibited EC growth in vivo. ( A ) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. ( B ) Representative images of xenograft tumors in shNC and shFBXL18 groups. ( C ) Tumor weights of shNC and shFBXL18 groups were measured at the end point. ( E ) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. ( F ) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: SiRNA specifically targeting DUSP16 or negative control siRNA (siNeg) were obtained from Sangon Biotech (Shanghai, China).

    Techniques: In Vivo, Western Blot, Quantitative RT-PCR