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MC1R种系变体赋予BRAF突变型黑色素瘤风险。

MC1R germline variants confer risk for BRAF-mutant melanoma.

作者信息

Landi Maria Teresa, Bauer Jürgen, Pfeiffer Ruth M, Elder David E, Hulley Benjamin, Minghetti Paola, Calista Donato, Kanetsky Peter A, Pinkel Daniel, Bastian Boris C

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

出版信息

Science. 2006 Jul 28;313(5786):521-2. doi: 10.1126/science.1127515. Epub 2006 Jun 29.

Abstract

Germline variants in MC1R, the gene encoding the melanocortin-1 receptor, and sun exposure increase risk for melanoma in Caucasians. The majority of melanomas that occur on skin with little evidence of chronic sun-induced damage (non-CSD melanoma) have mutations in the BRAF oncogene, whereas in melanomas on skin with marked CSD (CSD melanoma) these mutations are less frequent. In two independent Caucasian populations, we show that MC1R variants are strongly associated with BRAF mutations in non-CSD melanomas. In this tumor subtype, the risk for melanoma associated with MC1R is due to an increase in risk of developing melanomas with BRAF mutations.

摘要

编码黑皮质素-1受体的基因MC1R中的种系变异以及日晒会增加白种人患黑色素瘤的风险。大多数发生在几乎没有慢性阳光损伤迹象的皮肤上的黑色素瘤(非慢性阳光损伤性黑色素瘤)具有BRAF癌基因突变,而在有明显慢性阳光损伤的皮肤上的黑色素瘤(慢性阳光损伤性黑色素瘤)中,这些突变则不太常见。在两个独立的白种人群体中,我们发现MC1R变异与非慢性阳光损伤性黑色素瘤中的BRAF突变密切相关。在这种肿瘤亚型中,与MC1R相关的黑色素瘤风险是由于发生BRAF突变的黑色素瘤风险增加所致。

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