Somatic Mutations Associated with Metastasis in Acral Melanoma


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

Acral melanoma is one of the most aggressive and fast-growing forms of cutaneous melanoma and is characterized by a predominant location on the palms and feet. Primary tumors, metastases, and normal tissue samples from five acral melanoma patients were examined by massive parallel sequencing, focusing on the coding regions of 4100 genes involved in the origin and progression of hereditary and oncology diseases. Somatic mutations were found in genes related to cell division, proliferation, and apoptosis (BRAF, NRAS, VAV1, GATA1, and GCM2); cell adhesion (CTNND2 and ITGB4); angiogenesis (VEGFA); and the regulation of energy metabolism (BCS1L). Comparisons of target DNA sequences between morphologically normal and primary tumor tissues and between normal and metastatic tissues identified the candidate genes responsible for rapid metastasis in acral melanoma.

Sobre autores

I. Abramov

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: nased@biochip.ru
Rússia, Moscow, 119991

M. Emelyanova

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: nased@biochip.ru
Rússia, Moscow, 119991

O. Ryabaya

Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation

Email: nased@biochip.ru
Rússia, Moscow, 115478

G. Krasnov

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: nased@biochip.ru
Rússia, Moscow, 119991

A. Zasedatelev

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: nased@biochip.ru
Rússia, Moscow, 119991

T. Nasedkina

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Autor responsável pela correspondência
Email: nased@biochip.ru
Rússia, Moscow, 119991

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Pleiades Publishing, Inc., 2019