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New RAD51 Inhibitors to Target Homologous Recombination in Human Cells

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 i...

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Autores principales: Shkundina, Irina S., Gall, Alexander A., Dick, Alexej, Cocklin, Simon, Mazin, Alexander V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235719/
https://www.ncbi.nlm.nih.gov/pubmed/34208492
http://dx.doi.org/10.3390/genes12060920
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author Shkundina, Irina S.
Gall, Alexander A.
Dick, Alexej
Cocklin, Simon
Mazin, Alexander V.
author_facet Shkundina, Irina S.
Gall, Alexander A.
Dick, Alexej
Cocklin, Simon
Mazin, Alexander V.
author_sort Shkundina, Irina S.
collection PubMed
description 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.
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spelling pubmed-82357192021-06-27 New RAD51 Inhibitors to Target Homologous Recombination in Human Cells Shkundina, Irina S. Gall, Alexander A. Dick, Alexej Cocklin, Simon Mazin, Alexander V. Genes (Basel) Article 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. MDPI 2021-06-16 /pmc/articles/PMC8235719/ /pubmed/34208492 http://dx.doi.org/10.3390/genes12060920 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shkundina, Irina S.
Gall, Alexander A.
Dick, Alexej
Cocklin, Simon
Mazin, Alexander V.
New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title_full New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title_fullStr New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title_full_unstemmed New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title_short New RAD51 Inhibitors to Target Homologous Recombination in Human Cells
title_sort new rad51 inhibitors to target homologous recombination in human cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235719/
https://www.ncbi.nlm.nih.gov/pubmed/34208492
http://dx.doi.org/10.3390/genes12060920
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