<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(23)</volume><submitter>Khanna A</submitter><pubmed_abstract>Residual androgen receptor (AR)-signaling and presence of cancer stem-like cells (SCs) are the two emerging paradigms for clinically challenging castration-resistant prostate cancer (CRPC). Therefore, identification of AR-target proteins that are also overexpressed in the cancer SC population would be an attractive therapeutic approach.Our analysis of over three hundred clinical samples and patient-derived prostate epithelial cultures (PPECs), revealed Cancerous inhibitor of protein phosphatase 2A (CIP2A) as one such target. CIP2A is significantly overexpressed in both hormone-naïve prostate cancer (HN-PC) and CRPC patients . CIP2A is also overexpressed, by 3- and 30-fold, in HN-PC and CRPC SCs respectively. In vivo binding of the AR to the intronic region of CIP2A and its functionality in</pubmed_abstract><journal>Oncotarget</journal><pagination>19661-70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4637312</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CIP2A is a candidate therapeutic target in clinically challenging prostate cancer cell populations.</pubmed_title><pmcid>PMC4637312</pmcid><pubmed_authors>Kivinummi KK</pubmed_authors><pubmed_authors>Helenius MA</pubmed_authors><pubmed_authors>Maitland NJ</pubmed_authors><pubmed_authors>Tolonen TT</pubmed_authors><pubmed_authors>Manni V</pubmed_authors><pubmed_authors>Latonen L</pubmed_authors><pubmed_authors>Saramaki OR</pubmed_authors><pubmed_authors>Visakorpi T</pubmed_authors><pubmed_authors>Khanna A</pubmed_authors><pubmed_authors>Urbanucci A</pubmed_authors><pubmed_authors>Pimanda JE</pubmed_authors><pubmed_authors>Rane JK</pubmed_authors><pubmed_authors>Westermarck J</pubmed_authors></additional><is_claimable>false</is_claimable><name>CIP2A is a candidate therapeutic target in clinically challenging prostate cancer cell populations.</name><description>Residual androgen receptor (AR)-signaling and presence of cancer stem-like cells (SCs) are the two emerging paradigms for clinically challenging castration-resistant prostate cancer (CRPC). Therefore, identification of AR-target proteins that are also overexpressed in the cancer SC population would be an attractive therapeutic approach.Our analysis of over three hundred clinical samples and patient-derived prostate epithelial cultures (PPECs), revealed Cancerous inhibitor of protein phosphatase 2A (CIP2A) as one such target. CIP2A is significantly overexpressed in both hormone-naïve prostate cancer (HN-PC) and CRPC patients . CIP2A is also overexpressed, by 3- and 30-fold, in HN-PC and CRPC SCs respectively. In vivo binding of the AR to the intronic region of CIP2A and its functionality in</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Aug</publication><modification>2026-05-09T15:49:56.041Z</modification><creation>2019-03-27T02:01:33Z</creation></dates><accession>S-EPMC4637312</accession><cross_references><pubmed>25965834</pubmed><doi>10.18632/oncotarget.3875</doi></cross_references></HashMap>