作为结直肠癌遗传测试组候选人的BRCA基因:系统审查和元分析
Zhewen Feng1, Xiaobao Yang1, Mingwei Tian1
1Department of General Surgery, Beijing Friendship Hospital, Capital Medical University & National Clinical Research Center for Digestive Diseases, No.95, Yong An Road, Xicheng District, Beijing, 100050, China.
BMC cancer
|August 29, 2023
概括
包括BRCA1和BRCA2在内的BRCA基因突变与结直肠癌的风险增加有关. 这些发现表明,BRCA基因可能是结直肠癌遗传测试面板的宝贵补充.
科学领域:
- 遗传学和基因组学 遗传学和基因组学
- 在瘤学瘤学.
- 癌症流行病学 癌症流行病学
背景情况:
- 乳腺癌易感基因 (BRCA) 是众所周知的几种癌症的风险因素.
- 在BRCA突变和结直肠癌 (CRC) 风险之间的关联仍然不清楚和争论.
- 这项研究调查了BRCA1和BRCA2突变与CRC风险之间的联系.
结论:
- BRCA 基因是结直肠癌发展的潜在风险因素.
- 在结直肠癌风险评估中,BRCA基因可能需要被纳入基因测试小组.
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