Ontology highlight
ABSTRACT: Background
Breast and ovarian cancers are common malignancies among women, contributing to a significant disease burden, and are characterized by a high level of genomic instability, owing to the failure of homologous recombination repair (HRR). Pharmacological inhibition of poly(ADP-ribose) polymerase (PARP) could elicit the synthetic lethal effect of tumor cells in patients with homologous recombination deficiency, ultimately achieving a favorable clinical benefit. However, primary and acquired resistance remain the greatest hurdle, limiting the efficacy of PARP inhibitors; thus, strategies conferring or augmenting tumor cell sensitivity to PARP inhibitors are urgently required.Methods
Our RNA-seq data of niraparib-treated and -untreated tumor cells were analyzed by R lan
SUBMITTER: Wang S
PROVIDER: S-EPMC9925261 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature