Antoniou A C, Easton D F
Cancer Research UK Genetic Epidemiology Unit, Department of Public Health and Primary Care, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK.
Oncogene. 2006 Sep 25;25(43):5898-905. doi: 10.1038/sj.onc.1209879.
One of the most important risk factors for breast cancer is family history of the disease, indicating that genetic factors are important determinants of breast cancer risk. A number of breast cancer susceptibility genes have been identified, the most important being BRCA1 and BRCA2. However, it is estimated that all the currently known breast cancer susceptibility genes accounts for less than 25% of the familial aggregation of breast cancer. In this paper, we review the evidence for other breast cancer susceptibility genes arising from twin studies, pedigree analysis and studies of phenotypes associated with breast cancer, and the progress towards finding other breast cancer susceptibility genes through linkage and association studies. Taken together, the available evidence indicates that susceptibility to breast cancer is mediated through variants in many genes, each conferring a moderate risk of the disease. Such a model of susceptibility has implications for both risk prediction and for future gene identification studies.
乳腺癌最重要的风险因素之一是该病的家族病史,这表明遗传因素是乳腺癌风险的重要决定因素。一些乳腺癌易感基因已被确定,其中最重要的是BRCA1和BRCA2。然而,据估计,目前所有已知的乳腺癌易感基因在乳腺癌家族聚集病例中所占比例不到25%。在本文中,我们综述了来自双胞胎研究、系谱分析以及与乳腺癌相关表型研究中有关其他乳腺癌易感基因的证据,以及通过连锁和关联研究寻找其他乳腺癌易感基因方面的进展。综合来看,现有证据表明,乳腺癌易感性是由许多基因中的变异介导的,每个基因都赋予该病一定程度的风险。这种易感性模型对风险预测和未来的基因识别研究都有影响。