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XRCC2  -  X-ray repair complementing defective...

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Disease relevance of XRCC2

  • Considering that the XRCC2 (R188H) allele reduces risk to epithelial ovarian cancer, the increased XRCC2 activity with the R188H polymorphism may have clinical benefit in preventing cancer risk [1].
 

High impact information on XRCC2

  • Interestingly, Xrcc2(-/-) DT40 cells complemented with variant XRCC2 (R188H) were more tolerant to cisplatin than those with wild-type XRCC2 [1].

References

  1. A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. Danoy, P., Sonoda, E., Lathrop, M., Takeda, S., Matsuda, F. Biochem. Biophys. Res. Commun. (2007) [Pubmed]
 
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