Ontology highlight
ABSTRACT: Background
Approximately half of high-grade serous ovarian carcinomas (HGSOCs) demonstrate homologous recombination repair (HR) pathway defects, resulting in a distinct clinical phenotype comprising hypersensitivity to platinum, superior clinical outcome, and greater sensitivity to poly(adenosine diphosphate-ribose) polymerase (PARP) inhibitors. EMSY, which is known to be amplified in breast and ovarian cancers, encodes a protein reported to bind and inactivate BRCA2. Thus, EMSY overexpression may mimic BRCA2 mutation, resulting in HR deficiency. However, to our knowledge, the phenotypic consequences of EMSY overexpression in HGSOC patients has not been explored.Methods
Here we investigate the impact of EMSY expression on clinical outcome and sensitivity to platinum-based c
SUBMITTER: Hollis RL
PROVIDER: S-EPMC6771827 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature