Srivastava, Mrinal and Raghavan, Sathees C (2015) DNA Double-Strand Break Repair Inhibitors as Cancer Therapeutics. In: CHEMISTRY & BIOLOGY, 22 (1). pp. 17-29.
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Abstract
Among DNA damages, double-strand breaks (DSBs) are one of the most harmful lesions to a cell. Failure in DSB repair could lead to genomic instability and cancer. Homologous recombination (HR) and nonhomologous end joining (NHEJ) are major DSB repair pathways in higher eukaryotes. It is known that expression of DSB repair genes is altered in various cancers. Activation of DSB repair genes is one of the reasons for chemo-and radioresistance. Therefore, targeting DSB repair is an attractive strategy to eliminate cancer. Besides, therapeutic agents introduce breaks in the genome as an intermediate. Therefore, blocking the residual repair using inhibitors can potentiate the efficacy of cancer treatment. In this review, we discuss the importance of targeting DSB repair pathways for the treatment of cancer. Recent advances in the development of DSB repair inhibitors and their clinical relevance are also addressed.
Item Type: | Journal Article |
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Publication: | CHEMISTRY & BIOLOGY |
Publisher: | CELL PRESS |
Additional Information: | Copy right for this article belongs to the CELL PRESS, 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, MA 02139 USA |
Department/Centre: | Division of Biological Sciences > Biochemistry |
Date Deposited: | 05 Mar 2015 12:58 |
Last Modified: | 05 Mar 2015 12:58 |
URI: | http://eprints.iisc.ac.in/id/eprint/51015 |
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