Department of Dermatology, Wellman Center for Photomedicine, 48 Blossom Street, Massachusetts General Hospital, Boston, MA 02114, USA.
Genome Med. 2009 Oct 27;1(10):95. doi: 10.1186/gm95.
Cutaneous malignancies, especially malignant melanoma, exhibit great genetic heterogeneity. As a result, some individuals and families have particularly increased risk due to genetic predisposition to the disease. The susceptibility alleles range from rarely occurring, heritable, high-risk variants to ubiquitously occurring low-risk variants. Although until now the focus has been mostly towards the familial high-risk genes, the development of genome-wide association studies has uncovered a number of moderate- to low-risk predisposition alleles. The ability to specifically identify genetic variation associated with visible pigmentation traits and disease risk has provided a much richer view of the genetics of cutaneous malignancies. In this review, we provide an update on the recently identified risk loci. Existing clinical data, combined with vast genome information, will provide a better understanding of the biology of disease, and increased accuracy in risk prediction.
皮肤恶性肿瘤,特别是恶性黑色素瘤,表现出极大的遗传异质性。因此,由于遗传易感性,一些个体和家族的患病风险特别高。易感等位基因的范围从罕见的、遗传性的、高风险变体到普遍存在的低风险变体。尽管到目前为止,研究的重点主要是家族性高风险基因,但全基因组关联研究的发展已经揭示了一些中低风险的易感性等位基因。能够特异性识别与可见色素沉着特征和疾病风险相关的遗传变异,为皮肤恶性肿瘤的遗传学提供了更丰富的视角。在这篇综述中,我们提供了最近发现的风险位点的最新信息。现有的临床数据,结合大量的基因组信息,将提供对疾病生物学的更好理解,并提高风险预测的准确性。