Chew H K
Division of Hematology/Oncology, University of California-Davis Cancer Center, 4501 X St, Ste 3016, Sacramento, CA 95817, USA.
Tex Med. 2001 Feb;97(2):40-5.
Although the etiology of most cancers is thought to be sporadic and multifactorial, 5% to 10% of breast, ovarian, and colon cancers result from defects or mutations in specific genes inherited by a person through the germline. Distinctions may be made between hereditary and sporadic cancers. Because the risk of developing cancer is greater for persons from a hereditary cancer family than for the general public, these people should be considered for early detection and prevention options. Testing for selected cancer genes is available commercially, and physicians must determine which patients are appropriate candidates for these tests. Risk-reduction strategies and options for high-risk patients as well as legal and ethical issues pertaining to genetic counseling and testing will be considered.
尽管大多数癌症的病因被认为是散发性的且由多种因素导致,但5%至10%的乳腺癌、卵巢癌和结肠癌是由个体通过生殖系遗传的特定基因缺陷或突变引起的。遗传性癌症和散发性癌症之间存在区别。由于来自遗传性癌症家族的人患癌症的风险高于普通公众,因此应考虑让这些人进行早期检测和预防。市面上有针对特定癌症基因的检测服务,医生必须确定哪些患者适合这些检测。本文将探讨高危患者的风险降低策略和选择,以及与遗传咨询和检测相关的法律和伦理问题。