| Literature DB >> 35373283 |
L Alexander Liggett1,2, Vijay G Sankaran1,2,3.
Abstract
SUMMARY: Inherited genetic variation is increasingly identified as an important predisposing factor to a variety of cancers. In this issue of Cancer Discovery, Pareja and colleagues developed a method of reliably detecting mosaic cancer susceptibility mutations in patients who have been sequenced as part of the MSK-IMPACT tumor profiling platform. This led to the identification of a number of mosaic mutations in cancer susceptibility alleles that are generally found in the germline, suggesting that many predisposition variants may be missed through conventional testing. See related article by Pareja et al., p. 949 (6). ©2022 American Association for Cancer Research.Entities:
Mesh:
Year: 2022 PMID: 35373283 PMCID: PMC8988512 DOI: 10.1158/2159-8290.CD-22-0025
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272