Metastatic melanoma is characterized by extremely poor survival rates and hence novel therapies are urgently required. The ability of many anticancer drugs to activate autophagy, a lysosomal-mediated catabolic process which usually promotes cell survival, suggests targeting the autophagy pathway may be a novel means to augment therapy.

Armstrong, J., Corazzari, M., Martin, S., Pagliarini, V., Falasca, L., Hill, D., et al. (2011). Oncogenic B-RAF signaling in melanoma impairs the therapeutic advantage of autophagy inhibition. CLINICAL CANCER RESEARCH, 17(8), 2216-2226 [10.1158/1078-0432.CCR-10-3003].

Oncogenic B-RAF signaling in melanoma impairs the therapeutic advantage of autophagy inhibition

CORAZZARI, MARCO;PIACENTINI, MAURO;
2011-04-15

Abstract

Metastatic melanoma is characterized by extremely poor survival rates and hence novel therapies are urgently required. The ability of many anticancer drugs to activate autophagy, a lysosomal-mediated catabolic process which usually promotes cell survival, suggests targeting the autophagy pathway may be a novel means to augment therapy.
15-apr-2011
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/06 - ANATOMIA COMPARATA E CITOLOGIA
English
Con Impact Factor ISI
Armstrong, J., Corazzari, M., Martin, S., Pagliarini, V., Falasca, L., Hill, D., et al. (2011). Oncogenic B-RAF signaling in melanoma impairs the therapeutic advantage of autophagy inhibition. CLINICAL CANCER RESEARCH, 17(8), 2216-2226 [10.1158/1078-0432.CCR-10-3003].
Armstrong, J; Corazzari, M; Martin, S; Pagliarini, V; Falasca, L; Hill, D; Ellis, N; Al Sabah, S; Redfern, C; Fimia, G; Piacentini, M; Lovat, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/19407
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