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Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 <t>(TEAD4).</t> (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.
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Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 <t>(TEAD4).</t> (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.
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Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 <t>(TEAD4).</t> (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.
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Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 <t>(TEAD4).</t> (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.
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Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 (TEAD4). (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.

Journal: Gut and Liver

Article Title: TEAD4 Transcriptionally Activates TRIB3 to Induce Ferroptosis Resistance through the MEK/ERK Signaling Pathway in Colorectal Cancer

doi: 10.5009/gnl240439

Figure Lengend Snippet: Upregulation of tribbles homolog 3 (TRIB3) by TEA domain transcription factor 4 (TEAD4). (A) Screening and correlation analysis of transcription factors closely related to TRIB3 overexpression according to bioinformatics analysis. (B) JASPRA online tool identification of the binding sites of TEAD4 and TRIB3. (C) Dual-luciferase reporter gene experiment verifying the binding of TEAD4 and TRIB3. (D) Chromatin immunoprecipitation experiment verifying the binding of TEAD4 and TRIB3. (E) Analysis of TEAD4 expression in colorectal cancer and normal tissues according to data from the Cancer Genome Atlas (TCGA) database. Green represents the expression of TEAD4 in normal tissues. Red represents the expression of TEAD4 in CRC tissues. (F) Real-time quantitative polymerase chain reaction measurement of TEAD4 mRNA expression in normal colonic epithelial cells and CRC cell lines (SW480, HCT116, and HT-29). NS, no significant difference; NC, negative control. *p<0.05.

Article Snippet: Immunoprecipitation was performed using protein A/G magnetic beads coupled with the anti-TEAD4 antibody (12418-1-AP) from Proteintech (Wuhan, China ), with IgG used as an NC.

Techniques: Over Expression, Binding Assay, Luciferase, Chromatin Immunoprecipitation, Expressing, Real-time Polymerase Chain Reaction, Negative Control

TEA domain transcription factor 4 (TEAD4) induces ferroptosis resistance of colorectal cancer by upregulating tribbles homolog 3 (TRIB3) to trigger the MEK/ERK signaling pathway. (A) Real-time quantitative polymerase chain reaction measurement of TRIB3 expression in each group. (B) Colony formation assay assessed cell proliferation. (C) Flow cytometry detected reactive oxygen species levels. (D) Reagent kit determined Fe 2+ levels. (E) Reagent kit determined glutathione (GSH) levels. (F) Reagent kit determined NADPH levels. (G) Western blot assessed expression levels of ferroptosis-related protein encoded by GPX4, SLC3A2, SLC7A11, and related pathway proteins MEK, p-MEK, ERK, p-ERK. NC, negative control; oe, overexpression. *p<0.05.

Journal: Gut and Liver

Article Title: TEAD4 Transcriptionally Activates TRIB3 to Induce Ferroptosis Resistance through the MEK/ERK Signaling Pathway in Colorectal Cancer

doi: 10.5009/gnl240439

Figure Lengend Snippet: TEA domain transcription factor 4 (TEAD4) induces ferroptosis resistance of colorectal cancer by upregulating tribbles homolog 3 (TRIB3) to trigger the MEK/ERK signaling pathway. (A) Real-time quantitative polymerase chain reaction measurement of TRIB3 expression in each group. (B) Colony formation assay assessed cell proliferation. (C) Flow cytometry detected reactive oxygen species levels. (D) Reagent kit determined Fe 2+ levels. (E) Reagent kit determined glutathione (GSH) levels. (F) Reagent kit determined NADPH levels. (G) Western blot assessed expression levels of ferroptosis-related protein encoded by GPX4, SLC3A2, SLC7A11, and related pathway proteins MEK, p-MEK, ERK, p-ERK. NC, negative control; oe, overexpression. *p<0.05.

Article Snippet: Immunoprecipitation was performed using protein A/G magnetic beads coupled with the anti-TEAD4 antibody (12418-1-AP) from Proteintech (Wuhan, China ), with IgG used as an NC.

Techniques: Real-time Polymerase Chain Reaction, Expressing, Colony Assay, Flow Cytometry, Western Blot, Negative Control, Over Expression