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The DNA damage response and cancer therapy
Abstract
Genomic instability is one of the most pervasive characteristics of tumour cells and is probably the combined effect of DNA damage, tumour-specific DNA repair defects, and a failure to stop or stall the cell cycle before the damaged DNA is passed on to daughter cells. Although these processes drive genomic instability and ultimately the disease process, they also provide therapeutic opportunities. A better understanding of the cellular response to DNA damage will not only inform our knowledge of cancer development but also help to refine the classification as well as the treatment of the disease.
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Organisms have evolved a complex network of DNA repair mechanisms that are collectively capable of dealing with most of the damage inflicted to nuclear DNA.
“To minimize these lesions, organisms have evolved a complex network of DNA repair mechanisms that are collectively capable of dealing with most of the damage inflicted to nuclear DNA (Lord and Ashworth, 2012).”
From The Hallmarks of Aging (2013) · cites this paper as Lord and Ashworth, 2012
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“Whereas small base adducts are repaired by BER, some of the bulkier single-strand lesions that distort the DNA helical structure, such as those caused by ultraviolet light, are processed by nucleotide excision repair (NER”
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Metadata
- Authors
- Lord, C. J., & Ashworth, A.
- Venue
- Nature
- Published
- 2012-01
- Volume
- 481
- Issue
- 7381
- Pages
- 287-294
- ISSN
- 0028-0836
- 1476-4687
- Cited by
- 1,649
- References
- 12
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
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