What is it about?
Genetic factors play an important role in colorectal cancer risk, yet the prevalence and spectrum of germline cancer susceptibility gene mutations among Chinese CRC patients is largely undetermined. In our study, gene mutations in Chinese CRC patients were detected by high-throughput targeted sequencing, aiming to explore the frequency and spectrum of cancer susceptibility gene germline mutations among Chinese CRC patients and identify the likely pathogenic mutations which were highly related to colorectal cancer.
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Why is it important?
Using a multigene panel testing, we determined the prevalence and spectrum of germline mutations in 74 genes associated with various hereditary cancer syndromes in 618 unselected CRC patients. Meanwhile we found genes currently unrelated to colorectal cancer and excluded from routine molecular diagnostic screens may be predisposed to CRC and 33 novel variants were discovered and evaluated as pathogenic mutations by our study.Finding new genetic factors related to colorectal cancer can not only help to clarify the pathogenesis of colorectal cancer, but also help to guide the clinical development of prevention and treatment strategies, provide a systematic monitoring and management of hereditary colorectal cancer.
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This page is a summary of: Mutation spectrum of germline cancer susceptibility genes among unselected Chinese colorectal cancer patients, Cancer Management and Research, April 2019, Dove Medical Press,
DOI: 10.2147/cmar.s193985.
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