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家族性黑色素瘤的遗传流行病学

Genetic epidemiology of familial melanoma.

作者信息

Goldstein A M, Tucker M A

机构信息

Genetic Epidemiology Branch, National Cancer Institute, Bethesda, Maryland, USA.

出版信息

Dermatol Clin. 1995 Jul;13(3):605-12.

PMID:7554508
Abstract

Genetic epidemiology focuses on the role of genetic factors and their interaction with environmental factors in the occurrence of disease. Approximately 8% to 12% of malignant melanoma cases occur in individuals with a familial predisposition. To date, loci on chromosomes 1p and 9p have been implicated in the development of familial melanoma. Genetic epidemiologic techniques provide tools to study the heterogeneity of familial melanoma and to examine the interaction between genetic and nongenetic components of melanoma. Management of high-risk individuals from melanoma-prone families should aim to prevent disease by reducing exposure to known and suspected risk factors and to detect early melanoma by recognizing and performing biopsies on suspicious-looking nevi.

摘要

遗传流行病学关注遗传因素及其与环境因素在疾病发生中的作用。约8%至12%的恶性黑色素瘤病例发生在有家族易感性的个体中。迄今为止,1号染色体和9号染色体上的位点已被认为与家族性黑色素瘤的发生有关。遗传流行病学技术为研究家族性黑色素瘤的异质性以及检测黑色素瘤遗传和非遗传成分之间的相互作用提供了工具。对黑色素瘤高发家族中的高危个体进行管理,应旨在通过减少接触已知和可疑的危险因素来预防疾病,并通过识别外观可疑的痣并进行活检来早期发现黑色素瘤。

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