生殖系
种系突变
癌症研究
生物
遗传学
突变
计算生物学
医学
基因
作者
Fang Wu,Xiaowen Wang,Hongmei Zhang
出处
期刊:PubMed
日期:2024-12-10
卷期号:41 (12): 1508-1515
标识
DOI:10.3760/cma.j.cn511374-20240419-00244
摘要
Malignant tumors are closely related to various genetic and environmental factors. Pathogenic germline gene mutations play a key role in the occurrence and development of some malignant tumors. Some germline mutations can increase the risk of malignant tumors. For example, those with homologous recombination repair gene BRCA1/2 mutations are prone to breast cancer, ovarian cancer, etc., and some germline mutations are associated with genetic syndromes. For instance, 80% of hereditary non-polyposis colon cancers are associated with mutations in mismatch repair genes such as MLH1 and MLH2. In addition, 70% of Li-Fraumeni syndrome patients have harbored germline TP53 mutations. With the development of next-generation sequencing technology, more and more germline gene mutations have been discovered recently, which is of great significance for the prevention, screening, and treatment of tumors. This article has provided a review for common germline mutations, detection methods, and advances in drug therapy.
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