Antitumor Potential of S-Nitrosothiol-Containing Polymeric Nanoparticles against Melanoma

Autor(es)

Ferraz, Leticia S. ^[1] ; Watashi, Carolina M. ^[1] ; Colturato-Kido, Carina ^[1] ; Pelegrino, Milena T. ^[1] ; Paredes-Gamero, Edgar J. ^[2] ; Weller, Richard B. ^[3] ; Seabra, Amedea B. ^{[1, 4]} ; Rodrigues, Tiago ^{[1, 4]}

Afiliação do(s) autor(es)

^[1] Fed Univ ABC UFABC, Ctr Nat & Human Sci CCNH, Sao Paulo - Brazil

^[2] UMC, Interdisciplinary Ctr Biochem Invest CIIB, BR-08780911 Sao Paulo - Brazil

^[3] Univ Edinburgh, Queens Med Res Inst, Ctr Inflammat Res, MRC, Edinburgh EH16 4TJ, Midlothian - Scotland

^[4] Fed Univ ABC UFABC, Nanomed Res Unit NANOMED, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: MOLECULAR PHARMACEUTICS; v. 15, n. 3, SI, p. 1160-1168, MAR 2018.
• Citações Web of Science: 4

Resumo

Melanoma is a malignant proliferative disease originated from melanocyte transformations, which are characterized by a high metastatic rate and mortality. Advances in Nanotechnology have provided useful new approaches and tools for antitumor chemotherapy. The aim of this study was to investigate the molecular mechanisms underlying chitosan nanoparticles containing S-nitrosomercaptosuccinic acid (S-nitroso-MSA-CS) induced cytotoxicity in melanoma cells. S-Nitroso-MSA-CS induced concentration dependent cell death against B16-F10 tumor cells, whereas non-nitroso nanopartides (CS or MSA-CS) did not induce significant cytotoxicity. Additionally, melanoma cells were more sensitive to cell death than normal melanocytes. S-Nitroso-MSA-CS-induced cytotoxicity exhibited features of caspase-dependent apoptosis, and it was associated with oxidative stress, characterized by increased mitochondrial superoxide production and oxidation of protein thiol groups. In addition, tyrosine nitration and cysteine S-nitrosylation of amino acid residues in cellular proteins were observed. The potential use of these nanoparticles in antitumor chemotherapy of melanoma is discussed. (AU)

• Processo FAPESP: 12/12247-8 - Novas aplicações de fenotiazinas e paladaciclos: utilização de sistemas nanoestruturados para o estudo dos mecanismos de morte em células tumorais
• Beneficiário: Tiago Rodrigues
• Linha de fomento: Auxílio à Pesquisa - Regular
• Processo FAPESP: 16/07367-5 - Investigação dos Mecanismos de Indução de Morte Celular por Fenotiazinas em Células Tumorais: Modulação da Expressão Gênica e Papel das Proteínas da Família BCL-2 e Estresse do Retículo Endoplasmático
• Beneficiário: Tiago Rodrigues
• Linha de fomento: Auxílio à Pesquisa - Regular