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黑色素瘤中不同的基因改变组合。

Distinct sets of genetic alterations in melanoma.

作者信息

Curtin John A, Fridlyand Jane, Kageshita Toshiro, Patel Hetal N, Busam Klaus J, Kutzner Heinz, Cho Kwang-Hyun, Aiba Setsuya, Bröcker Eva-Bettina, LeBoit Philip E, Pinkel Dan, Bastian Boris C

机构信息

Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94143-0808, USA.

出版信息

N Engl J Med. 2005 Nov 17;353(20):2135-47. doi: 10.1056/NEJMoa050092.

Abstract

BACKGROUND

Exposure to ultraviolet light is a major causative factor in melanoma, although the relationship between risk and exposure is complex. We hypothesized that the clinical heterogeneity is explained by genetically distinct types of melanoma with different susceptibility to ultraviolet light.

METHODS

We compared genome-wide alterations in the number of copies of DNA and mutational status of BRAF and N-RAS in 126 melanomas from four groups in which the degree of exposure to ultraviolet light differs: 30 melanomas from skin with chronic sun-induced damage and 40 melanomas from skin without such damage; 36 melanomas from palms, soles, and subungual (acral) sites; and 20 mucosal melanomas.

RESULTS

We found significant differences in the frequencies of regional changes in the number of copies of DNA and mutation frequencies in BRAF among the four groups of melanomas. Samples could be correctly classified into the four groups with 70 percent accuracy on the basis of the changes in the number of copies of genomic DNA. In two-way comparisons, melanomas arising on skin with signs of chronic sun-induced damage and skin without such signs could be correctly classified with 84 percent accuracy. Acral melanoma could be distinguished from mucosal melanoma with 89 percent accuracy. Eighty-one percent of melanomas on skin without chronic sun-induced damage had mutations in BRAF or N-RAS; the majority of melanomas in the other groups had mutations in neither gene. Melanomas with wild-type BRAF or N-RAS frequently had increases in the number of copies of the genes for cyclin-dependent kinase 4 (CDK4) and cyclin D1 (CCND1), downstream components of the RAS-BRAF pathway.

CONCLUSIONS

The genetic alterations identified in melanomas at different sites and with different levels of sun exposure indicate that there are distinct genetic pathways in the development of melanoma and implicate CDK4 and CCND1 as independent oncogenes in melanomas without mutations in BRAF or N-RAS.

摘要

背景

紫外线暴露是黑色素瘤的主要致病因素,尽管风险与暴露之间的关系很复杂。我们推测临床异质性是由对紫外线敏感性不同的基因不同类型的黑色素瘤所解释的。

方法

我们比较了四组紫外线暴露程度不同的126例黑色素瘤中DNA拷贝数的全基因组改变以及BRAF和N-RAS的突变状态:30例来自有慢性阳光损伤皮肤的黑色素瘤和40例来自无此类损伤皮肤的黑色素瘤;36例来自手掌、足底和甲下(肢端)部位的黑色素瘤;以及20例黏膜黑色素瘤。

结果

我们发现四组黑色素瘤中DNA拷贝数的区域变化频率和BRAF的突变频率存在显著差异。根据基因组DNA拷贝数的变化,样本能够以70%的准确率正确分类为四组。在两组比较中,有慢性阳光损伤迹象的皮肤和无此类迹象的皮肤产生的黑色素瘤能够以84%的准确率正确分类。肢端黑色素瘤与黏膜黑色素瘤的区分准确率为89%。无慢性阳光损伤的皮肤中的黑色素瘤有81%在BRAF或N-RAS中有突变;其他组的大多数黑色素瘤在这两个基因中均无突变。BRAF或N-RAS为野生型的黑色素瘤中,细胞周期蛋白依赖性激酶4(CDK4)和细胞周期蛋白D1(CCND1)基因的拷贝数经常增加,它们是RAS-BRAF途径的下游成分。

结论

在不同部位和不同阳光暴露水平的黑色素瘤中发现的基因改变表明,黑色素瘤的发生存在不同的遗传途径,并表明CDK4和CCND1在BRAF或N-RAS无突变的黑色素瘤中作为独立的癌基因发挥作用。

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