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黑素皮质素受体1(MC1R)变体在葡萄膜黑色素瘤中的作用。

Role of MC1R variants in uveal melanoma.

作者信息

Hearle N, Humphreys J, Damato B E, Wort R, Talaban R, Wixey J, Green H, Easton D F, Houlston R S

机构信息

Haddow Laboratories, Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton SM2 5NG, UK.

出版信息

Br J Cancer. 2003 Nov 17;89(10):1961-5. doi: 10.1038/sj.bjc.6601358.

Abstract

Variants of the melanocortin-1 receptor (MC1R) gene have been linked to sun-sensitive skin types and hair colour, and may independently play a role in susceptibility to cutaneous melanoma. To assess the role of MC1R variants in uveal melanoma, we have analysed a cohort of 350 patients for the changes within the major region of the gene displaying sequence variation. Eight variants were detected - V60L, D84E, V92M, R151C, I155T, R160W, R163Q and D294H - 63% of these patients being hetero- or homozygous for at least one variant. Standard melanoma risk factor data were available on 119 of the patients. MC1R variants were significantly associated with hair colour (P=0.03) but not skin or eye colour. The frequency of the variants detected in the 350 patients was comparable with those in the general population, and comparison of the cumulative tumour distribution by age at diagnosis in carriers and noncarriers provided no evidence that MC1R variants confer an increased risk of uveal melanoma. We interpret the data as indicating that MC1R variants do not appear to be major determinants of susceptibility to uveal melanoma.

摘要

黑皮质素-1受体(MC1R)基因的变体与对阳光敏感的皮肤类型和头发颜色有关,并且可能独立地在皮肤黑色素瘤易感性中发挥作用。为了评估MC1R变体在葡萄膜黑色素瘤中的作用,我们分析了350例患者队列中该基因主要区域内显示序列变异的变化情况。检测到8种变体——V60L、D84E、V92M、R151C、I155T、R160W、R163Q和D294H——其中63%的患者至少有一种变体为杂合子或纯合子。119例患者有标准的黑色素瘤风险因素数据。MC1R变体与头发颜色显著相关(P=0.03),但与皮肤或眼睛颜色无关。在350例患者中检测到的变体频率与一般人群中的频率相当,并且对携带者和非携带者按诊断年龄的累积肿瘤分布进行比较,没有证据表明MC1R变体增加葡萄膜黑色素瘤的风险。我们将这些数据解释为表明MC1R变体似乎不是葡萄膜黑色素瘤易感性的主要决定因素。

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