Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Clin Genet. 2013 Nov;84(5):407-14. doi: 10.1111/cge.12256. Epub 2013 Sep 12.
Women with a family history of breast cancer have an approximately twofold elevated risk of the disease. Even though an array of genes has been associated with breast cancer risk the past two decades, variants within these genes jointly explain at most 40% of this familial risk. Many explanations for this 'missing heritability' have been proposed, including the existence of many very rare variants, interactions between genetic and environmental factors and structural genetic variation. In this review, we discuss how next generation sequencing will teach us more about the genetic architecture of breast cancer, with a specific focus on very rare genetic variants. While such variants potentially explain a substantial proportion of familial breast cancer, assessing the breast cancer risks conferred by them remains challenging, even if this risk is relatively high. To assess more moderate risks, epidemiological approaches will require very large patient cohorts to be genotyped for the variant, only achievable through international collaboration. How well we will be able to eventually resolve the missing heritability for breast cancer in a clinically meaningful way crucially depends on the underlying complexity of the genetic architecture.
有乳腺癌家族史的女性患病风险大约增加两倍。尽管过去二十年中已经有一系列基因与乳腺癌风险相关,但这些基因中的变异最多只能解释家族风险的 40%。对于这种“遗传缺失”有许多解释,包括许多非常罕见的变异、遗传和环境因素之间的相互作用以及结构性遗传变异。在这篇综述中,我们讨论了下一代测序将如何帮助我们更多地了解乳腺癌的遗传结构,特别关注非常罕见的遗传变异。虽然这些变异可能解释了家族性乳腺癌的很大一部分,但评估它们所带来的乳腺癌风险仍然具有挑战性,即使这种风险相对较高。为了评估更中等程度的风险,流行病学方法需要对大量患者进行该变异的基因分型,这只能通过国际合作实现。我们最终能否以一种具有临床意义的方式很好地解决乳腺癌的遗传缺失,在很大程度上取决于遗传结构的潜在复杂性。