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Circadian clock, cancer, and chemotherapy

Authors
Sancar, A.Lindsey-Boltz, L.A.Gaddameedhi, S.Selby, C.P.Ye, R.Chiou, Y.-Y.Kemp, M.G.Hu, J.Lee, J.H.Ozturk, N.
Issue Date
2015
Publisher
American Chemical Society
Citation
Biochemistry, v.54, no.2, pp.110 - 123
Indexed
SCIE
SCOPUS
Journal Title
Biochemistry
Volume
54
Number
2
Start Page
110
End Page
123
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/95903
DOI
10.1021/bi5007354
ISSN
0006-2960
Abstract
The circadian clock is a global regulatory system that interfaces with most other regulatory systems and pathways in mammalian organisms. Investigations of the circadian clock-DNA damage response connections have revealed that nucleotide excision repair, DNA damage checkpoints, and apoptosis are appreciably influenced by the clock. Although several epidemiological studies in humans and a limited number of genetic studies in mouse model systems have indicated that clock disruption may predispose mammals to cancer, well-controlled genetic studies in mice have not supported the commonly held view that circadian clock disruption is a cancer risk factor. In fact, in the appropriate genetic background, clock disruption may instead aid in cancer regression by promoting intrinsic and extrinsic apoptosis. Finally, the clock may affect the efficacy of cancer treatment (chronochemotherapy) by modulating the pharmacokinetics and pharmacodynamics of chemotherapeutic drugs as well as the activity of the DNA repair enzymes that repair the DNA damage caused by anticancer drugs. © 2014 American Chemical Society.
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