Affiliation:
1. From the Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, London, United Kingdom
Abstract
Cancer cells frequently harbor defects in DNA repair pathways, leading to genomic instability. This can foster tumorigenesis but also provides a weakness in the tumor that can be exploited therapeutically. Tumors with compromised ability to repair double-strand DNA breaks by homologous recombination, including those with defects in BRCA1 and BRCA2, are highly sensitive to blockade of the repair of DNA single-strand breaks via the inhibition of the enzyme poly(ADP) ribose polymerase. This provides the basis for a novel synthetic lethal approach to cancer therapy.
Publisher
American Society of Clinical Oncology (ASCO)
Cited by
741 articles.
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