<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hoppe MM</submitter><funding>Cancer Research UK</funding><funding>National Research Foundation Singapore</funding><funding>National Medical Research Council</funding><pagination>e13366</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8103098</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>Early relapse after platinum chemotherapy in epithelial ovarian cancer (EOC) portends poor survival. A-priori identification of platinum resistance is therefore crucial to improve on standard first-line carboplatin-paclitaxel treatment. The DNA repair pathway homologous recombination (HR) repairs platinum-induced damage, and the HR recombinase RAD51 is overexpressed in cancer. We therefore designed a REMARK-compliant study of pre-treatment RAD51 expression in EOC, using fluorescent quantitative immunohistochemistry (qIHC) to overcome challenges in quantitation of protein expression in situ. In a discovery cohort (n = 284), RAD51-High tumours had shorter progression-free and overall survival compared to RAD51-Low cases in univariate and multivariate analyses. The association of RAD51 with r</pubmed_abstract><journal>EMBO molecular medicine</journal><pubmed_title>Quantitative imaging of RAD51 expression as a marker of platinum resistance in ovarian cancer.</pubmed_title><pmcid>PMC8103098</pmcid><funding_grant_id>NMRC/TA/0052/2016</funding_grant_id><funding_grant_id>NMRC/CIRG/1400/2014</funding_grant_id><funding_grant_id>NMRC/CSA‐INV/0016/2017</funding_grant_id><pubmed_authors>Jaynes P</pubmed_authors><pubmed_authors>Sedukhina AS</pubmed_authors><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Choi H</pubmed_authors><pubmed_authors>Upadhyayula SS</pubmed_authors><pubmed_authors>Pitt JJ</pubmed_authors><pubmed_authors>Jeyasekharan AD</pubmed_authors><pubmed_authors>Lim DGZ</pubmed_authors><pubmed_authors>Wardyn JD</pubmed_authors><pubmed_authors>Karnezis A</pubmed_authors><pubmed_authors>Huntsman DG</pubmed_authors><pubmed_authors>Pang BNK</pubmed_authors><pubmed_authors>Tan TZ</pubmed_authors><pubmed_authors>P S Yeong J</pubmed_authors><pubmed_authors>Scott CL</pubmed_authors><pubmed_authors>Chiu DS</pubmed_authors><pubmed_authors>Tan DSP</pubmed_authors><pubmed_authors>Topp MD</pubmed_authors><pubmed_authors>Patel NR</pubmed_authors><pubmed_authors>Lie S</pubmed_authors><pubmed_authors>Sato K</pubmed_authors><pubmed_authors>Hoppe MM</pubmed_authors><pubmed_authors>Kaye SB</pubmed_authors><pubmed_authors>Leung S</pubmed_authors><pubmed_authors>Brown R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative imaging of RAD51 expression as a marker of platinum resistance in ovarian cancer.</name><description>Early relapse after platinum chemotherapy in epithelial ovarian cancer (EOC) portends poor survival. A-priori identification of platinum resistance is therefore crucial to improve on standard first-line carboplatin-paclitaxel treatment. The DNA repair pathway homologous recombination (HR) repairs platinum-induced damage, and the HR recombinase RAD51 is overexpressed in cancer. We therefore designed a REMARK-compliant study of pre-treatment RAD51 expression in EOC, using fluorescent quantitative immunohistochemistry (qIHC) to overcome challenges in quantitation of protein expression in situ. In a discovery cohort (n = 284), RAD51-High tumours had shorter progression-free and overall survival compared to RAD51-Low cases in univariate and multivariate analyses. The association of RAD51 with r</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-05-09T08:20:05.364Z</modification><creation>2022-02-10T09:57:05.099Z</creation></dates><accession>S-EPMC8103098</accession><cross_references><pubmed>33709473</pubmed><doi>10.15252/emmm.202013366</doi></cross_references></HashMap>