Petrakis N L, King M C
Cancer. 1977 Apr;39(4 Suppl):1861-6. doi: 10.1002/1097-0142(197704)39:4+<1861::aid-cncr2820390819>3.0.co;2-i.
The study of potential associations between genetic markers and various cancers has a long history in cancer epidemiology. Such investigations are subject to serious problems of statistical significance and the choice of appropriate control populations. A promising future for the use of human population genetics in cancer epidemiology may be in the investigation of genetic markers (such as the HL-A complex) which code for proteins of potential immunological or physiological importance in susceptibility or resistance to cancer. The cerumen gentic marker has played a central part in a hypothesis formulated in our laboratory for the etiology of breast cancer. A second new development in this field is likely to be the investigation of genetic markers in families with high incidence of cancer. Such families permit the simultaneous study of genetic hypotheses of cancer inheritance and the association of marker genotypes with cancer through segregation and linkage analysis.
在癌症流行病学中,对基因标记与各种癌症之间潜在关联的研究由来已久。此类调查存在统计学显著性的严重问题以及合适对照人群的选择问题。在癌症流行病学中使用人类群体遗传学的一个有前景的未来可能在于对基因标记(如HL - A复合体)的研究,这些基因标记编码在癌症易感性或抗性方面具有潜在免疫或生理重要性的蛋白质。耳垢基因标记在我们实验室提出的乳腺癌病因假说中起到了核心作用。该领域的第二个新进展可能是对癌症高发家族中的基因标记进行研究。此类家族允许通过分离分析和连锁分析同时研究癌症遗传的基因假说以及标记基因型与癌症的关联。