Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/39130
Title: Mastoparan induces apoptosis in B1 6F10-Nex2 melanoma cells via the intrinsic mitochondrial pathway and displays antitumor activity in vivo
Authors: Azevedo, Ricardo A. de
Figueiredo, Carlos R. [UNIFESP]
Ferreira, Adilson K.
Matsuo, Alisson L. [UNIFESP]
Massaoka, Mariana H. [UNIFESP]
Girola, Natalia [UNIFESP]
Auada, Aline V. V.
Farias, Camyla F. [UNIFESP]
Pasqualoto, Kerly F. M.
Rodrigues, Cecilia P.
Barbuto, Jose A.
Levy, Debora
Bydlowski, Sergio P.
Sa-Junior, Paulo L. de
Travassos, Luiz R. [UNIFESP]
Lebrun, Ivo
Butantan Inst
Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Keywords: Mastoparan
Apoptosis
Intrinsic pathway
Melanoma
Antitumor effects in vivo
Issue Date: 1-Jun-2015
Publisher: Elsevier B.V.
Citation: Peptides. New York: Elsevier B.V., v. 68, p. 113-119, 2015.
Abstract: Mastoparan is an a-helical and amphipathic tetradecapeptide obtained from the venom of the wasp Vespula lewisii. This peptide exhibits a wide variety of biological effects, including antimicrobial activity, increased histamine release from mast cells, induction of a potent mitochondrial permeability transition and tumor cell cytotoxicity. Here, the effects of mastoparan in malignant melanoma were studied using the murine model of B16F10-Nex2 cells. in vitro, mastoparan caused melanoma cell death by the mitochondrial apoptosis pathway, as evidenced by the Annexin V-FITC/PI assay, loss of mitochondrial membrane potential (Delta psi(m)), generation of reactive oxygen species, DNA degradation and cell death signaling. Most importantly, mastoparan reduced the growth of subcutaneous melanoma in syngeneic mice and increased their survival. the present results show that mastoparan induced caspase-dependent apoptosis in melanoma cells through the intrinsic mitochondrial pathway protecting the mice against tumor development. (C) 2014 Elsevier Inc. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/39130
ISSN: 0196-9781
Other Identifiers: http://dx.doi.org/10.1016/j.peptides.2014.09.024
Appears in Collections:Em verificação - Geral

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