Synthesis and biological evaluation of DIDS analogues as efficient inhibitors of RAD51 involved in homologous recombination-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of DIDS analogues as efficient inhibitors of RAD51 involved in homologous recombination

Published:2023-05 Issue: Volume:87 Page:129261
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Demeyer Alexandre,Fonteneau Lucie,Liennard Marion,Foyer Claire^ORCID,Weigel Pierre,Laurent Adèle D.,Lebreton Jacques^ORCID,Fleury Fabrice,Mathé-Allainmat Monique^ORCID

Funder

Université de Nantes

Société d'Accélération du Transfert de Technologies

Centre National de la Recherche Scientifique

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference33 articles.

1. Targeting homologous recombination, new pre-clinical and clinical therapeutic combinations inhibiting RAD51;Ward;Cancer Treat Rev,2015

2. Resveratrol decreases Rad51 expression and sensitizes cisplatin-resistant MCF-7 breast cancer cells;Leon-Galicia;Oncol Rep,2018

3. High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient’s outcome;Barbano;Int J Cancer,2011

4. PARP Inhibition in Cancer: An Update on Clinical Development;Sachdev;Target Oncol,2019

5. RAD51 as a potential surrogate marker for DNA repair capacity in solid malignancies;Gachechiladze;Int J Cancer,2017

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