<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(2)</volume><submitter>Palassin P</submitter><pubmed_abstract>&lt;b>Aim:&lt;/b> The transcription factor RIP140 (receptor interacting protein of 140 kDa) is involved in intestinal tumorigenesis. It plays a role in the control of microsatellite instability (MSI), through the regulation of &lt;i>MSH2&lt;/i> and &lt;i>MSH6&lt;/i> gene expression. The aim of this study was to explore its effect on the expression of &lt;i>POLK&lt;/i>, the gene encoding the specialized translesion synthesis (TLS) DNA polymerase κ known to perform accurate DNA synthesis at microsatellites. &lt;b>Methods:&lt;/b> Different mouse models and engineered human colorectal cancer (CRC) cell lines were used to analyze by RT-qPCR, while Western blotting and luciferase assays were used to elucidate the role of RIP140 on &lt;i>POLK&lt;/i> gene expression. Published DNA microarray datasets were reanalyzed. The &lt;i>in vitro</pubmed_abstract><journal>Cancer drug resistance (Alhambra, Calif.)</journal><pagination>401-414</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9255241</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>RIP140 regulates &lt;i>POLK&lt;/i> gene expression and the response to alkylating drugs in colon cancer cells.</pubmed_title><pmcid>PMC9255241</pmcid><pubmed_authors>Castet-Nicolas A</pubmed_authors><pubmed_authors>Cavailles V</pubmed_authors><pubmed_authors>Gyorffy B</pubmed_authors><pubmed_authors>Lapierre M</pubmed_authors><pubmed_authors>Teyssier C</pubmed_authors><pubmed_authors>Pillaire MJ</pubmed_authors><pubmed_authors>Hoffmann JS</pubmed_authors><pubmed_authors>Palassin P</pubmed_authors><pubmed_authors>Bonnet S</pubmed_authors><pubmed_authors>Jalaguier S</pubmed_authors></additional><is_claimable>false</is_claimable><name>RIP140 regulates &lt;i>POLK&lt;/i> gene expression and the response to alkylating drugs in colon cancer cells.</name><description>&lt;b>Aim:&lt;/b> The transcription factor RIP140 (receptor interacting protein of 140 kDa) is involved in intestinal tumorigenesis. It plays a role in the control of microsatellite instability (MSI), through the regulation of &lt;i>MSH2&lt;/i> and &lt;i>MSH6&lt;/i> gene expression. The aim of this study was to explore its effect on the expression of &lt;i>POLK&lt;/i>, the gene encoding the specialized translesion synthesis (TLS) DNA polymerase κ known to perform accurate DNA synthesis at microsatellites. &lt;b>Methods:&lt;/b> Different mouse models and engineered human colorectal cancer (CRC) cell lines were used to analyze by RT-qPCR, while Western blotting and luciferase assays were used to elucidate the role of RIP140 on &lt;i>POLK&lt;/i> gene expression. Published DNA microarray datasets were reanalyzed. The &lt;i>in vitro</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T10:43:36.948Z</modification><creation>2022-07-23T10:14:45.014Z</creation></dates><accession>S-EPMC9255241</accession><cross_references><pubmed>35800380</pubmed><doi>10.20517/cdr.2021.133</doi></cross_references></HashMap>