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jak stat signaling pathway inhibitor linderalactone  (MedChemExpress)


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    MedChemExpress jak stat signaling pathway inhibitor linderalactone
    Jak Stat Signaling Pathway Inhibitor Linderalactone, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/jak+stat+inhibitor+jak/Linderalactone/pm42247295-217-11-16
    Average 94 stars, based on 3 article reviews
    jak stat signaling pathway inhibitor linderalactone - by Bioz Stars, 2026-09
    94/100 stars

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    Article Title: CCL25/CCR9-induced M2 macrophage polarization promotes lung cancer progression via TGF-β1-mediated activation of the JAK/STAT-PIM2 signaling pathway.
    Article Snippet: significantly improved the prognosis of some patients, but key bottlenecks such as tumor heterogeneity, drug resistance, and dysregulated tumor microenvironment (TME) regulation still exist.. Particularly for highly malignant tumors like lung cancer, the therapeutic effect remains to be improved.. Lung cancer (LC) is the second most prevalent malignancy globally and a prominent cause of cancer-related mortality [2].



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    MedChemExpress jak stat pathway inhibitors ruxolitinib
    A Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transduced with a doxycycline-inducible ADAR1 -targeting shRNA and exposed to a titration of doxycycline (ng/mL). Data representative of n = 2 biologically-independent experiments. B , C RT-qPCR of IFNB1 ( B ) and CCL5 ( C ) mRNAs in SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA. IFNB1 and CCL5 mRNAs were analyzed separately relative to GAPDH . Box-and-whiskers show arbitrary units of gene expression normalized to the BRCA1 -mutant siCTRL condition; N = 4 values from individual measurements, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ***[ IFNB1 , BRCA1 -Rev, siADAR1 1.25 nM]=0.0002, ****< 0.0001. D Western blot of MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data representative of n = 2 biologically-independent experiments. E , F RT-qPCR of Ifnb1 ( E ) and Ccl5 ( F ) mRNAs in MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data presented as in ( B , C ). P values, ****< 0.0001. G , H Clonogenic survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Violin plots indicate median, lower and upper quartiles; N = 6 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. I Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Data representative of n = 3 biologically-independent experiments. J , K Cell survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA in the context of exposure to the JAK/STAT pathway <t>inhibitors</t> (JSPi) <t>ruxolitinib</t> ( J ; 10 µM) or upadacitinib ( K ; 32 µM). Box-and-whiskers indicate median, lower and upper quartiles, and the min to max range; N = 4 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. siCTRL, non-targeting, negative control siRNA; siPLK1, PLK1 -targeting, positive control siRNA. Source data are provided as a Source Data file.
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    A Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transduced with a doxycycline-inducible ADAR1 -targeting shRNA and exposed to a titration of doxycycline (ng/mL). Data representative of n = 2 biologically-independent experiments. B , C RT-qPCR of IFNB1 ( B ) and CCL5 ( C ) mRNAs in SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA. IFNB1 and CCL5 mRNAs were analyzed separately relative to GAPDH . Box-and-whiskers show arbitrary units of gene expression normalized to the BRCA1 -mutant siCTRL condition; N = 4 values from individual measurements, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ***[ IFNB1 , BRCA1 -Rev, siADAR1 1.25 nM]=0.0002, ****< 0.0001. D Western blot of MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data representative of n = 2 biologically-independent experiments. E , F RT-qPCR of Ifnb1 ( E ) and Ccl5 ( F ) mRNAs in MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data presented as in ( B , C ). P values, ****< 0.0001. G , H Clonogenic survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Violin plots indicate median, lower and upper quartiles; N = 6 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. I Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Data representative of n = 3 biologically-independent experiments. J , K Cell survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA in the context of exposure to the JAK/STAT pathway <t>inhibitors</t> (JSPi) <t>ruxolitinib</t> ( J ; 10 µM) or upadacitinib ( K ; 32 µM). Box-and-whiskers indicate median, lower and upper quartiles, and the min to max range; N = 4 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. siCTRL, non-targeting, negative control siRNA; siPLK1, PLK1 -targeting, positive control siRNA. Source data are provided as a Source Data file.
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    A Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transduced with a doxycycline-inducible ADAR1 -targeting shRNA and exposed to a titration of doxycycline (ng/mL). Data representative of n = 2 biologically-independent experiments. B , C RT-qPCR of IFNB1 ( B ) and CCL5 ( C ) mRNAs in SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA. IFNB1 and CCL5 mRNAs were analyzed separately relative to GAPDH . Box-and-whiskers show arbitrary units of gene expression normalized to the BRCA1 -mutant siCTRL condition; N = 4 values from individual measurements, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ***[ IFNB1 , BRCA1 -Rev, siADAR1 1.25 nM]=0.0002, ****< 0.0001. D Western blot of MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data representative of n = 2 biologically-independent experiments. E , F RT-qPCR of Ifnb1 ( E ) and Ccl5 ( F ) mRNAs in MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data presented as in ( B , C ). P values, ****< 0.0001. G , H Clonogenic survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Violin plots indicate median, lower and upper quartiles; N = 6 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. I Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Data representative of n = 3 biologically-independent experiments. J , K Cell survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA in the context of exposure to the JAK/STAT pathway <t>inhibitors</t> (JSPi) <t>ruxolitinib</t> ( J ; 10 µM) or upadacitinib ( K ; 32 µM). Box-and-whiskers indicate median, lower and upper quartiles, and the min to max range; N = 4 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. siCTRL, non-targeting, negative control siRNA; siPLK1, PLK1 -targeting, positive control siRNA. Source data are provided as a Source Data file.
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    Image Search Results


    A Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transduced with a doxycycline-inducible ADAR1 -targeting shRNA and exposed to a titration of doxycycline (ng/mL). Data representative of n = 2 biologically-independent experiments. B , C RT-qPCR of IFNB1 ( B ) and CCL5 ( C ) mRNAs in SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA. IFNB1 and CCL5 mRNAs were analyzed separately relative to GAPDH . Box-and-whiskers show arbitrary units of gene expression normalized to the BRCA1 -mutant siCTRL condition; N = 4 values from individual measurements, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ***[ IFNB1 , BRCA1 -Rev, siADAR1 1.25 nM]=0.0002, ****< 0.0001. D Western blot of MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data representative of n = 2 biologically-independent experiments. E , F RT-qPCR of Ifnb1 ( E ) and Ccl5 ( F ) mRNAs in MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data presented as in ( B , C ). P values, ****< 0.0001. G , H Clonogenic survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Violin plots indicate median, lower and upper quartiles; N = 6 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. I Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Data representative of n = 3 biologically-independent experiments. J , K Cell survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA in the context of exposure to the JAK/STAT pathway inhibitors (JSPi) ruxolitinib ( J ; 10 µM) or upadacitinib ( K ; 32 µM). Box-and-whiskers indicate median, lower and upper quartiles, and the min to max range; N = 4 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. siCTRL, non-targeting, negative control siRNA; siPLK1, PLK1 -targeting, positive control siRNA. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Autocrine interferon poisoning mediates ADAR1-dependent synthetic lethality in BRCA1/2 -mutant cancers

    doi: 10.1038/s41467-025-62309-5

    Figure Lengend Snippet: A Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transduced with a doxycycline-inducible ADAR1 -targeting shRNA and exposed to a titration of doxycycline (ng/mL). Data representative of n = 2 biologically-independent experiments. B , C RT-qPCR of IFNB1 ( B ) and CCL5 ( C ) mRNAs in SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA. IFNB1 and CCL5 mRNAs were analyzed separately relative to GAPDH . Box-and-whiskers show arbitrary units of gene expression normalized to the BRCA1 -mutant siCTRL condition; N = 4 values from individual measurements, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ***[ IFNB1 , BRCA1 -Rev, siADAR1 1.25 nM]=0.0002, ****< 0.0001. D Western blot of MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data representative of n = 2 biologically-independent experiments. E , F RT-qPCR of Ifnb1 ( E ) and Ccl5 ( F ) mRNAs in MEF Brca1 -wildtype (WT) and Brca1 -mutant (Δ11) cells transfected with a concentration range (nM) of Adar1 siRNA. Data presented as in ( B , C ). P values, ****< 0.0001. G , H Clonogenic survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Violin plots indicate median, lower and upper quartiles; N = 6 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. I Western blot of SUM149 BRCA1 -Mut and BRCA1 -Rev cells subjected to co-transfection with ADAR1 siRNA and one of a series of siRNAs targeting pattern recognition receptors. Data representative of n = 3 biologically-independent experiments. J , K Cell survival of SUM149 BRCA1 -Mut and BRCA1 -Rev cells transfected with a concentration range (nM) of ADAR1 siRNA in the context of exposure to the JAK/STAT pathway inhibitors (JSPi) ruxolitinib ( J ; 10 µM) or upadacitinib ( K ; 32 µM). Box-and-whiskers indicate median, lower and upper quartiles, and the min to max range; N = 4 values from individual wells, representative of n = 3 biologically-independent experiments, two-way ANOVA post hoc Dunnett’s test. P values, ****< 0.0001. siCTRL, non-targeting, negative control siRNA; siPLK1, PLK1 -targeting, positive control siRNA. Source data are provided as a Source Data file.

    Article Snippet: The JAK/STAT pathway inhibitors ruxolitinib (INCB-18424; JAK1/2i), upadacitinib (ABT-494; JAK1i) and deucravacitinib (BMS-986165, TYK2i), and the integrated stress response inhibitor ISRIB were purchased from MedChemExpress.

    Techniques: Western Blot, Transduction, shRNA, Titration, Quantitative RT-PCR, Transfection, Concentration Assay, Gene Expression, Mutagenesis, Cotransfection, Negative Control, Positive Control