Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 1 | SUMO1 conjugation drives the cell cycle progression through G1/S transition. (a) Normal human brain and glioblastoma tissue samples were examined by western blotting using the indicated antibodies (left). b-Actin was used as the protein loading control and the molecular weight were indicated (left). (b) Three human astrocyte samples and two glioblastoma cell lines (top) were tested by western blotting for the expression of SUMO1-conjugated proteins and CDK6. (c) LN229 cells were transduced or not with the empty, scramble control, SUMO1 shRNA as indicated (top) and examined by western blotting using a SUMO1 antibody. (d) Three cell lines transduced with the shRNAs (top) were analysed for cell growth for 4 days (points: means; scale bar, s.e.; n ¼ 6 from two independent experiments; ***Po0.001; student’s t-test). (e,f) The transduced cell lines were analysed by flow cytometry for cell cycle (e) and bromodeoxyuridine (BrdU) incorporation (f) (points: means; scale bar, s.d.; n ¼ 3 from two independent experiments; ***Po0.001; student’s t-test).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Conjugation Assay, Western Blot, Control, Molecular Weight, Expressing, shRNA, Transduction, Cytometry, BrdU Incorporation Assay

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 2 | SUMO1 and CDK6 are required for glioblastoma progression. (a) Three cell lines were transduced or not with the indicated vectors (top) and subjected to western blotting using the antibodies as indicated (left). (b) The SUMO1–613 and control shRNA-expressing LN229 cells were transfected either with YFP-SUMO1 or His-SUMO1 and examined by western blotting using CDK6, His and GFP antibody that also recognized YFP. (c) Total RNA isolated from the cells as described above in (a) was examined by real-time PCR and the mRNA levels of SUMO1 and CDK6 were normalized to the control b-Actin mRNA levels (points: means; scale bar, s.d.; n ¼ 6 from two independent experiments; ***Po0.001; **Po0.01; NS: no significance; student’s t-test). (d) Kaplan–Meier curves show the survival of the mice transplanted intracranially with LN229 cells transduced or not with the indicated shRNA vectors (n ¼ 10 for each group; ***Po0.001; Log-rank test).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Western Blot, Control, shRNA, Expressing, Transfection, Isolation, Real-time Polymerase Chain Reaction

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 3 | SUMO1 and CDK6 contributes to the tumorigenesis of neurospheres. (a) Three neurospheres were transduced or not with the SUMO1 and CDK6 shRNAs as indicated (top) and tested by western blotting using SUMO1 and CDK6 antibodies. (b) The transduced neurospheres were examined by cell growth for 9 days (points: means; scale bar, s.d.; n ¼ 6 from two independent experiments; ***Po0.001; student’s t-test). (c) The transduced neurospheres were also examined by sphere formation assay with the numbers of neurospheres as indicated (left) (points: means; scale bar, s.d.; n ¼ 6 from three independent experiments; ***Po0.001; student’s t-test). (d,e) Coronal cerebral section (d) and microscopic section of hematoxylin and eosin (e) reveals the infiltrating glioblastoma on the right side of a mouse brain injected with the neurospheres expressing the control scrambled shRNA. (f,g) The glioblastoma xenograft was not observed in the mouse brain injected with the neurospheres-expressing shRNA targeting SUMO1 (f) or CDK6 shRNA (g). (h) Kaplan–Meier curves show the survival of the mice intracranially injected with the neurospheres transduced with the indicated shRNA vectors (n ¼ 6 for each group; ***Po0.001; Log-rank test).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Western Blot, Tube Formation Assay, Injection, Expressing, Control, shRNA, Transduction

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 4 | CDK6 is conjugated by SUMO1 but not SUMO2/3. (a) In vitro SUMOylation assay was performed in a reaction with the elements as indicated (top) and examined by western blotting using a CDK6 antibody with the free and conjugated forms of CDK6 indicated (right). (b) Three cell lines were lysed in a denaturing buffer, IPed with a CDK6 antibody with IgG used as a negative IP control and examined by western blotting using SUMO1 and CDK6 antibody. (c) LN229 cells were lysed in a denaturing buffer supplemented with or without NEM and the endogenous CDK6 protein was immunoprecipitated using a CDK6 antibody with IgG as control and tested examined by western blotting using SUMO1 and another CDK6 antibody. (d) LN229 cells transduced or not with SUMO1 and control shRNA (top) were transfected with Flag-CDK6 and myc-UBC9 (left top). Flag IP and whole-cell lysate (WCL) were tested by western blotting for the interaction of Ubc9 and CDK6. (e) LN229 cells were co-transfected with the indicated vectors (top), immunoprecipitated with a CDK6 antibody and examined by western blotting for the presence of Flag-CDK6-His-SUMO1 conjugates (right). (f) LN229 cells were co-transfected with YFP-SUMO3, YFP-SUMO1 and/or Flag-CDK6 and then immunoprecipitated with a Flag antibody. Western blotting using CDK6 and GFP antibody that recognizes YFP detected SUMO1–CDK6 conjugates as indicated (right). (g) Flag immunoprecipitate from YFP- SUMO1, Flag-CDK4 and Flag-CDK6 transfected LN229 cells were examined by western blotting for the presence of Flag-CDK6-YFP-SUMO1 conjugates.

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: In Vitro, Western Blot, Control, Immunoprecipitation, shRNA, Transfection

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 5 | SUMO1 is conjugated to the non-consensus Lys 216 on CDK6 protein. (a) The amino-acid sequence of CDK6 reveals 18 lysine residues as indicated (red). (b) Each of the 18 Lys (K) residues was replaced with an arginine (R) through point mutagenesis. Flag-tagged CDK6 wt and K–R mt were transfected with YFP-SUMO1 in LN229 cells. The transfected cells were lysed in a denaturing and diluted in a non-denaturing buffer. The cell lysates were immunoprecipitated with a Flag antibody and examined by western blotting using the indicated antibodies (left), revealing YFP-SUMO1-Flag- CDK6 conjugates in the cells transfected with all except K216R (arrow). (c) In vitro SUMOylation assay was carried out in the reaction with the indicated elements (top) and the reaction was analysed by western blotting using a CDK6 antibody. (d) SUMO1 and control shRNA-expressing LN229 cells were transfected with Flag-CDK6 wt and K–R mt. Flag IPs were subjected to kinase assay (top panel) and, together with whole-cell lysate (WCL), examined by western blotting (bottom panel).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Sequencing, Mutagenesis, Transfection, Immunoprecipitation, Western Blot, In Vitro, Control, shRNA, Expressing, Kinase Assay

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 6 | CDK6 SUMOylation inhibits its ubiquitination and degradation. (a) LN229 cells, transduced or not with the indicated shRNAs, were treated with MG132 for the indicated hours (top) and examined by western blotting using the indicated antibodies (left). (b) The transduced cells were IPed by a CDK6 antibody. The IP and whole-cell lysate (WCL) were examined by western blotting using UB and another CDK6 antibody. (c) The half-life of Flag-CDK6 protein was evaluated by western blotting (top) and quantified against the control b-actin protein in SUMO1 and control shRNA-expressing cells (bottom). (d) SUMO1 shRNA-expressing LN229 cells were transfected with Flag-CDK6 wt and K–R mt with HA-K48-polyubiquitin (HA-K48-UB). Flag immunoprecipitates were examined by western blotting using HA and CDK6 antibodies. (e) The SUMO1–613 shRNA-expressing LN229 cells were transfected with Flag-CDK6 wt, K147R and empty vector and analysed by western blotting (top) and cell growth assay (bottom) (points: means; scale bar, s.d.; n ¼ 6 from two independent experiments; ***Po0.001; student’s t-test).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Ubiquitin Proteomics, Western Blot, Control, shRNA, Expressing, Transfection, Plasmid Preparation, Growth Assay

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 7 | SUMOylation and ubiquitination regulate CDK6 degradation. (a) Flag-CDK6 wt, K216R and K147R mt were transfected in LN229 cells with HA-K48R polyubiquitin (HA-48-UB), HA-ubiquitin (HA-UB) and/or non-conjugated ubiquitin mt (K0-UB) in the concentrations as indicated (top). Flag-CDK6 and HA-ubiquitin were detected by western blotting using Flag and HA antibodies. (b) The half-life of Flag-CDK6 K216R and K147R mt were evaluated by western blotting (top) and quantified against the control b-actin in SUMO1 and control shRNA-expressing cells (bottom) (points: means; scale bar, s.d.; n ¼ 6 from two independent experiments). (c) The CDK6 protein structure, generated at http://www.rcsb.org (PDB 2EUF), shows the kinase active site with the ATP binding side chains in the deep cleft between N-terminal and C-terminal lobe from which T-loop arises. K216 of the C-terminal is close to K147 near the kinase active site. (d) LN229 cells were transfected with Flag-CDK6, HA-K48-UB, HA-UB and YFP-SUMO1. Flag IPes and whole-cell lysates (WCL) were tested by western blotting using the indicated antibodies (left).

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Ubiquitin Proteomics, Transfection, Western Blot, Control, shRNA, Expressing, Generated, Binding Assay

Journal: Nature communications

Article Title: SUMO1 modification stabilizes CDK6 protein and drives the cell cycle and glioblastoma progression.

doi: 10.1038/ncomms5234

Figure Lengend Snippet: Figure 8 | CDK1 activity phosphorylates UBC9 for CDK6 SUMOylation. (a) YFP-SUMO1 and Flag-CDK6-expressing LN229 cells were immuno- precipitated in the hours after release from nocodazole synchronization to the cell cycle as monitored by flow cytometry (low panel). Flag IPes and whole- cell lysate (WCL) were analysed by western blotting with asynchronized cells used as controls (top panel). (b) LN229 cells were co-transfected with YFP-SUMO1 and Flag-CDK6, treated with nocodazole for 20 h and then treated or not with RO-3306 for the indicated hours (top). Flag IP and WCL were analysed by western blotting using the indicated antibodies (left). (c) In vitro SUMOylation of CDK6 in the absence and presence of the cyclin B1–CDK1 complex (CDK1/Cycl B1). (d) HEK293 cells were expressed with the tagged proteins, immunoprecipitated and analysed by western blotting (top) and CDK1 kinase assay (bottom). (e) Flag-CDK6 was transfected with Myc-UBC9 wt or S71D mt in LN229 cells, immunoprecipitated using Flag antibodies and tested by western blotting for UBC9–CDK6 interaction. (f) LN229 cells were transfected with Myc-UBC9 WT and S71A mt together with Flag-CDK6 and/or YFP-SUMO1, immunoprecipitated and examined by western blotting. (g) The molecular model shows that CDK1 phosphorylates UBC9 and thus enhances SUMO1–CDK6 conjugation from G2/M to G1 phase, driving the cell cycle through G1/S transition.

Article Snippet: The reagents used in the study included anti-Flag M2 agarose (Sigma-Aldrich), Flag and myc peptide (Sigma-Aldrich), recombinant CDK6 (Signal Chem), SUMO1, Sea1/Sea2 (Aos1/Uba2, Boston Biochem, Boston), ovalbumin (Sigma), ATP (Boston Biochem), protease inhibitors (Sigma), ubiquitin E1 enzyme, UBC13, UBC5a, ubiquitin, K63 only ubiquitin, K48 only ubiquitin, K0 ubiquitin mt (Boston Biochem), truncated Rb (Signal Chem), kinase buffer (NEB), UBC9 (Boston Biochem), Histone H1 (NEB), CDK1–Cyclin-B1, CDK4–cyclin D1, CDK6–cyclin D1 and CDK2–cyclin E1 complex (Invitrogen), TNT Quick coupled Transcription/Translation system (Promega), Kinase-Glo Luminescent Kinase Assay reagent (Promega) and Hoechst 33342 (Molecular Probes). shRNA sequences and transduction.

Techniques: Activity Assay, Expressing, Cytometry, Western Blot, Transfection, In Vitro, Immunoprecipitation, Kinase Assay, Conjugation Assay

Journal: Cancer cell international

Article Title: MicroRNA-550a-3-5p controls the brain metastasis of lung cancer by directly targeting YAP1.

doi: 10.1186/s12935-021-02197-z

Figure Lengend Snippet: Fig. 7 The effects of miR-550a-3-5p on cleaved-PARP, pRB, CDK6, YAP1, CTGF, and CYR61. A Western blotting images. B Cleaved-PARP protein expression. C pRB protein expression. D CDK6 protein expression. E YAP1 protein expression. F CTGF protein expression. (G) CYR61 protein expression. *P < 0.05, compared with the control group; #P < 0.05, compared with the miR-550a-3-5p mimics group

Article Snippet: After blocking with 5% skim milk, the membranes were incubated with anti-cleaved-Poly(ADP-ribose) polymerase (PARP) antibody (1:1000, Abcam), anti-RB transcriptional corepressor 1 (pRB) antibody (1:1000, Abcam), anti-cyclin dependent kinase 6 (CDK6) antibody (1:1000, Abcam), anti-Yes1 associated transcriptional regulator (YAP1) antibody (1:1000, Abcam), anti- connective tissue growth factor (CTGF) antibody (1:1000, Proteintech Group, Inc.), anti-cysteine rich angiogenic inducer 61 (CYR61) antibody (1:1000, Abcam), and anti-GAPDH antibody (1:10,000, Proteintech Group, Inc.) overnight at 4 °C.

Techniques: Western Blot, Expressing, Control

Journal: Oncology reports

Article Title: miR-3619-5p inhibits prostate cancer cell growth by activating CDKN1A expression.

doi: 10.3892/or.2016.5250

Figure Lengend Snippet: Figure 6. miR-3619-5p inhibits cell cycle related gene expression primarily by regulating CDKN1A expression. DU145 and PC3 cells were transfected with 50 nM of the indicated RNAs for 72 h. (A) Expression of p21 mRNA was assessed by real-time PCR. GAPDH served as a loading control. (B) Induction of p21 protein expression was detected by western blot analysis. GAPDH were also detected and served as a loading control. (C) Expression of cyclin D1, CDK4 and CDK6 mRNA was detected by real-time PCR. GAPDH served as a loading control. (D) Expression of cyclin D1, CDK4 and CDK6 mRNA was determined by western blot analysis. α-Tublin served as a loading control. *P<0.05, **P<0.01 and ***P<0.001.

Article Snippet: After blocking the membranes were incubated overnight at 4 ̊C with appropriate dilutions of specific primary antibodies as follows: p21 (1/2000) (Cell Signaling Technology), cyclin D1 (1/2000) (Affinity, USA), CDK4 (1/1000) (Affinity), CDK6 (1/2000) (Affinity), GAPDH (1/500) (Boster, Wuhan, China) and α-tubulin (1/500) (Boster).

Techniques: Gene Expression, Expressing, Transfection, Real-time Polymerase Chain Reaction, Control, Western Blot

Journal: International Journal of Molecular Medicine

Article Title: Tribbles pseudokinase 3 drives cancer stemness in oral squamous cell carcinoma cells by supporting the expression levels of SOX2 and EGFR

doi: 10.3892/ijmm.2025.5485

Figure Lengend Snippet: TRIB3 depletion decreases cell proliferation and affects cell cycle distribution. (A) SAS and HSC3 oral squamous cell carcinoma cells were transduced with lentiviruses carrying shRNA sequences for LacZ (control), sh-TRIB3#1 or sh-TRIB3#2. Western blotting results confirmed TRIB3 protein knockdown. Cell proliferation was assessed by clonogenic assay, with colonies stained using crystal violet and visualized on day 14. (B) SAS and (C) HSC3 cells were transfected with siRNA NC or siTRIB3 for 48 h. Cells were then harvested for western blotting analysis to verify TRIB3 protein depletion and for cell cycle analysis using BrdU. Anti-BrdU-FITC and PI fluorescence signals were detected using flow cytometry, analyzed using FlowJo software (version 10; FlowJo LLC; BD Biosciences) and quantified. Data represented the percentage of cells at each cycle phase and were presented as mean ± SD. (D) Western blotting analysis was used to determine the protein expression levels of cell cycle regulators Cyclin A2, Cyclin B1 and Cyclin D1 following TRIB3 shRNA transfection for 48 h in SAS and HSC3 cells. For quantification, CDK1 and CDK6 levels were normalized to Tubulin using the upper TRIB3 blot, while Cyclin A2, Cyclin B1 and Cyclin D1 levels were normalized to GAPDH using the lower TRIB3 blot. Blot images were representative of one of three independent experiments. Statistical analyses were conducted using one-way ANOVA with post-hoc Tukey's Honestly Significant Difference test. * P<0.05; ** P<0.01; *** P<0.001. TRIB3, tribbles pseudokinase 3; shRNA, short hairpin RNA; siRNA, small interfering RNA; BrdU, 5-bromo-2-deoxyuridine; NC, negative control; si, siRNA.

Article Snippet: In the present study, the decreased expression of the CDK6 protein in SAS and HSC3 cells was observed following knockdown of TRIB3.

Techniques: Transduction, shRNA, Control, Western Blot, Knockdown, Clonogenic Assay, Staining, Transfection, Cell Cycle Assay, Fluorescence, Flow Cytometry, Software, Expressing, Small Interfering RNA, Negative Control

Journal: International Journal of Molecular Medicine

Article Title: Tribbles pseudokinase 3 drives cancer stemness in oral squamous cell carcinoma cells by supporting the expression levels of SOX2 and EGFR

doi: 10.3892/ijmm.2025.5485

Figure Lengend Snippet: Knockdown of TRIB3 downregulates cell cycle and stemness markers in xenograft tumors. Tumors derived from SAS cells transduced with shLacZ or shTRIB3 were analyzed by immunohistochemistry. Sections were stained for (A) TRIB3, (B) E2F1, (C) SOX2, (D) CDK1, (E) CDK6 and (F) EGFR. Representative immunohistochemical images are presented for each protein. Quantification of positive cells for each marker are presented. Staining intensities were quantitatively assessed from two random objective fields across three independent tumor sections per group. Data are presented as mean ± SD. Statistical analysis was performed using the unpaired Student's t-test. Scale bar, 50 μ m. TRIB3, tribbles pseudokinase 3; E2F1, E2F transcription factor 1; sh, short hairpin RNA.

Article Snippet: In the present study, the decreased expression of the CDK6 protein in SAS and HSC3 cells was observed following knockdown of TRIB3.

Techniques: Knockdown, Derivative Assay, Transduction, Immunohistochemistry, Staining, Immunohistochemical staining, Marker, shRNA