| Literature DB >> 34208492 |
Irina S Shkundina1, Alexander A Gall2, Alexej Dick1, Simon Cocklin1, Alexander V Mazin1,3.
Abstract
Targeting DNA repair proteins with small-molecule inhibitors became a proven anti-cancer strategy. Previously, we identified an inhibitor of a major protein of homologous recombination (HR) RAD51, named B02. B02 inhibited HR in human cells and sensitized them to chemotherapeutic drugs in vitro and in vivo. Here, using a medicinal chemistry approach, we aimed to improve the potency of B02. We identified the B02 analog, B02-isomer, which inhibits HR in human cells with significantly higher efficiency. We also show that B02-iso sensitizes triple-negative breast cancer MDA-MB-231 cells to the PARP inhibitor (PARPi) olaparib.Entities:
Keywords: DNA repair; homologous recombination; small-molecule inhibitors; triple-negative breast cancer
Year: 2021 PMID: 34208492 DOI: 10.3390/genes12060920
Source DB: PubMed Journal: Genes (Basel) ISSN: 2073-4425 Impact factor: 4.096