| Literature DB >> 29345160 |
Aaron Phelan1, Antonio Lopez-Beltran2, Rodolfo Montironi3, Shaobo Zhang1, Maria R Raspollini4, Monica Cheng1, Hristos Z Kaimakliotis5, Michael O Koch5, Liang Cheng1,5.
Abstract
Environmental factors that play a role in the urothelial carcinogenesis have been well characterized. Current research is continuously exploring potential heritable forms of bladder cancer. Lynch syndrome is a well-known inheritable disease that increases the risk for a variety of cancers, including urothelial carcinomas. Screening of patients with known Lynch syndrome is important to evaluate for development of new primary tumors. Further study may provide more information on what level of follow-up each patient needs. Recent data suggest that mismatch repair mutations confer a greater risk for urothelial cancer. Additional large patient series as well as advancement of molecular testing may provide triage for Lynch syndrome patients in regards to the frequency and type of screening best suited for individual patient.Entities:
Keywords: Lynch syndrome; bladder cancer; genetic susceptibility; microsatellite instability; mismatch repair deficiency; molecular genetics; upper urinary tract cancer
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Year: 2018 PMID: 29345160 DOI: 10.2217/fon-2017-0346
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404