<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(10)</volume><submitter>Zhang Y</submitter><pubmed_abstract>Unlike many other human solid tumors, ovarian tumors express many epithelial markers at a high level for cell growth and local invasion. The phosphoprotein Pinin plays a key role in epithelial cell identity. We showed that clinical ovarian tumors and ovarian cancer cell lines express a high level of Pinin when compared with normal ovarian tissues and immortalized normal ovarian surface epithelial cell lines. Pinin co-localized and physically interacted with transcriptional corepressor C-terminal binding proteins, CtBP1 and CtBP2, in the nuclei of cancer cells. Knockdown of Pinin in ovarian cancer cells resulted in specific reduction of CtBP1 protein expression, cell adhesion, anchorage-independent growth, and increased drug sensitivity. Whole transcriptomic comparison of next-generation RN</pubmed_abstract><journal>Oncotarget</journal><pagination>11397-411</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4905481</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pinin interacts with C-terminal binding proteins for RNA alternative splicing and epithelial cell identity of human ovarian cancer cells.</pubmed_title><pmcid>PMC4905481</pmcid><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Sugrue SP</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Ng SK</pubmed_authors><pubmed_authors>Muto MG</pubmed_authors><pubmed_authors>Tsui SK</pubmed_authors><pubmed_authors>Choi PW</pubmed_authors><pubmed_authors>Kwok JS</pubmed_authors><pubmed_authors>Welch WR</pubmed_authors><pubmed_authors>Ng SW</pubmed_authors><pubmed_authors>Berkowitz RS</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Singh M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pinin interacts with C-terminal binding proteins for RNA alternative splicing and epithelial cell identity of human ovarian cancer cells.</name><description>Unlike many other human solid tumors, ovarian tumors express many epithelial markers at a high level for cell growth and local invasion. The phosphoprotein Pinin plays a key role in epithelial cell identity. We showed that clinical ovarian tumors and ovarian cancer cell lines express a high level of Pinin when compared with normal ovarian tissues and immortalized normal ovarian surface epithelial cell lines. Pinin co-localized and physically interacted with transcriptional corepressor C-terminal binding proteins, CtBP1 and CtBP2, in the nuclei of cancer cells. Knockdown of Pinin in ovarian cancer cells resulted in specific reduction of CtBP1 protein expression, cell adhesion, anchorage-independent growth, and increased drug sensitivity. Whole transcriptomic comparison of next-generation RN</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2026-05-30T04:23:54.253Z</modification><creation>2019-03-27T02:15:54Z</creation></dates><accession>S-EPMC4905481</accession><cross_references><pubmed>26871283</pubmed><doi>10.18632/oncotarget.7242</doi></cross_references></HashMap>