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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Violacein induces death of RAS-mutated metastatic melanoma by impairing autophagy process

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Goncalves, Paola R. ; Rocha-Brito, Karin J. P. ; Fernandes, Maruska R. N. ; Abrantes, Julia L. ; Duran, Nelson ; Ferreira-Halder, Carmen V.
Número total de Autores: 6
Tipo de documento: Artigo Científico
Fonte: TUMOR BIOLOGY; v. 37, n. 10, p. 14049-14058, OCT 2016.
Citações Web of Science: 4

Treatment of metastatic melanoma still remains a challenge, since in advanced stage it is refractory to conventional treatments. Most patients with melanoma have either B-RAF or N-RAS mutations, and these oncogenes lead to activation of the RAS-RAF-MEK-ERK and AKT signal pathway, keeping active the proliferation and survival pathways in the cell. Therefore, the identification of small molecules that block metastatic cell proliferation and induce cell death is needed. Violacein, a pigment produced by Chromobacterium violaceum found in Amazon River, has been used by our group as a biotool for scrutinizing signaling pathways associated with proliferation, survival, aggressiveness, and resistance of cancer cells. In the present study, we demonstrate that violacein diminished the viability of RAS- and RAF-mutated melanoma cells (IC50 value similar to 500 nM), and more important, this effect was not abolished after treatment medium removal. Furthermore, violacein was able to reduce significantly the invasion capacity of metastatic melanoma cells in 3D culture. In the molecular context, we have shown for the first time that violacein causes a strong drop on histone deacetylase 6 expression, a proliferating activator, in melanoma cells. Besides, an inhibition of AXL and AKT was detected. All these molecular events propitiate an inhibition of autophagy, and consequently, melanoma cell death by apoptosis. (AU)

Processo FAPESP: 13/08896-3 - Mapeamento bioquímico do mecanismo antitumoral do calix[6]areno em célula humana de câncer de pâncreas: investigação do tráfego intracelular, do perfil kinômico e da expressão de microRNAs
Beneficiário:Karin Juliane Pelizzaro Rocha
Linha de fomento: Bolsas no Brasil - Pós-Doutorado