Genetic Epidemiology Branch/Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.
Pigment Cell Melanoma Res. 2010 Oct;23(5):587-606. doi: 10.1111/j.1755-148X.2010.00730.x. Epub 2010 Jul 16.
Recent genome-wide association studies (GWAS) identified genetic loci associated with pigmentation, nevi, and skin cancer. We performed a review and meta-analysis of GWAS results, grouping them into four categories: (i) loci associated with pigmentation (hair, eye, and/or skin color), cutaneous UV-response (sun sensitivity and/or freckling), and skin cancer; (ii) loci associated with nevi and melanoma; (iii) loci associated with pigmentation and/or cutaneous UV-response but not skin cancer; and (iv) loci associated distinctly with skin cancer, mostly basal cell carcinoma, but not pigmentation or cutaneous UV-response. These findings suggest at least two pathways for melanoma development (via pigmentation and via nevi), and two pathways for basal cell carcinoma development (via pigmentation and independent of pigmentation). However, further work is necessary to separate the association with skin cancer from the association with pigmentation. As with any GWAS, the identified loci may not include the causal variants and may need confirmation by direct genome sequencing.
最近的全基因组关联研究 (GWAS) 确定了与色素沉着、痣和皮肤癌相关的遗传位点。我们对 GWAS 结果进行了综述和荟萃分析,将它们分为四类:(i) 与色素沉着(头发、眼睛和/或皮肤颜色)、皮肤对紫外线的反应(日晒敏感性和/或雀斑)和皮肤癌相关的位点;(ii) 与痣和黑色素瘤相关的位点;(iii) 与色素沉着和/或皮肤对紫外线的反应相关但与皮肤癌无关的位点;(iv) 与皮肤癌(主要是基底细胞癌)相关但与色素沉着或皮肤对紫外线的反应无关的位点。这些发现表明黑色素瘤的发展至少有两种途径(通过色素沉着和通过痣),基底细胞癌的发展也有两种途径(通过色素沉着和独立于色素沉着)。然而,需要进一步的工作来将与皮肤癌的关联与与色素沉着的关联区分开来。与任何 GWAS 一样,所确定的位点可能不包括因果变异,并且可能需要通过直接基因组测序来确认。