癌症
微卫星不稳定性
体细胞
基因
突变
种系突变
生物
肿瘤科
BAP1型
医学
内科学
遗传学
生物信息学
微卫星
等位基因
作者
Constance H. Li,Syed Haider,Yu-Jia Shiah,Kevin Thai,Paul C. Boutros
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2018-10-01
卷期号:78 (19): 5527-5537
被引量:108
标识
DOI:10.1158/0008-5472.can-18-0362
摘要
Abstract Cancer differs significantly between men and women; even after adjusting for known epidemiologic risk factors, the sexes differ in incidence, outcome, and response to therapy. These differences occur in many but not all tumor types, and their origins remain largely unknown. Here, we compare somatic mutation profiles between tumors arising in men and in women. We discovered large differences in mutation density and sex biases in the frequency of mutation of specific genes; these differences may be associated with sex biases in DNA mismatch repair genes or microsatellite instability. Sex-biased genes include well-known drivers of cancer such as β-catenin and BAP1. Sex influenced biomarkers of patient outcome, where different genes were associated with tumor aggression in each sex. These data call for increased study and consideration of the molecular role of sex in cancer etiology, progression, treatment, and personalized therapy. Significance: This study provides a comprehensive catalog of sex differences in somatic alterations, including in cancer driver genes, which influence prognostic biomarkers that predict patient outcome after definitive local therapy. Cancer Res; 78(19); 5527–37. ©2018 AACR.
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