MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1056/nejmoa050092

Медицинская библиотека · The New England journal of medicine · 2005

Distinct sets of genetic alterations in melanoma.

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

Сравнительное исследованиеСтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

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.

Для цитирования: 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. Distinct sets of genetic alterations in melanoma.. The New England journal of medicine. 2005. DOI: 10.1056/nejmoa050092.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.