Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34704
Title: Autophagy inhibited Ehrlich ascitic tumor cells apoptosis induced by the nitrostyrene derivative compounds: Relationship with cytosolic calcium mobilization
Authors: Calgarotto, Andrana K.
Silva Pereira, Gustavo J. da [UNIFESP]
Bechara, Alexandre [UNIFESP]
Paredes-Gamero, Edgar J. [UNIFESP]
Barbosa, Christiano M. V. [UNIFESP]
Hirata, Hanako [UNIFESP]
Souza Queiroz, Mary L. de
Smaili, Soraya Soubhi [UNIFESP]
Bincoletto, Claudia [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual de Campinas (UNICAMP)
Keywords: Nitrostyrene derivative compounds
Autophagy
Cancer cells
Apoptosis
Calcium signaling
Issue Date: 5-Mar-2012
Publisher: Elsevier B.V.
Citation: European Journal of Pharmacology. Amsterdam: Elsevier B.V., v. 678, n. 1-3, p. 6-14, 2012.
Abstract: Apoptosis induction is often associated with increased autophagy, indicating interplay between these two important cellular events in cell death and survival. in this study, the programmed cell death and autophagy induced by two nitrostyrene derivative compounds (NTS1 and NTS2) was studied using the tumorigenic Ehrlich ascitic tumor (EAT) cells. EAT cells were highly sensitive to NTS1 and NTS2 cytotoxicity in a dose-dependent manner. NTS1 and NTS2 IC50 was less than 15.0 mu M post 12 h incubation. Apoptosis was primarily induced by both compounds, as demonstrated by an increase in Annexin-V positive cells, concurrently with cytochrome c release from mitochondria to cytosol and caspase-3 activation. Although cytosolic Ca2+ mobilization is involved in autophagy as well as apoptosis in response to cellular stress in many cancer cell types, from the two nitrostyrene derivative compounds studied, mainly NTS1 mobilized this ion and disparate autophagy in EAT cells. These results suggest that EAT induced cell death by NTS1 and NTS2 involved a Ca2+-dependent and a Ca2+-independent pathways, respectively. in accordance with these results, the treatment of EAT cells with 3 methyladenine (3-MA), an autophagy inhibitor; significantly increased the number of apoptotic cells after NTS1 treatment, suggesting that pharmacological modulation of autophagy augments the NTS1 efficacy. Thus, we denote the importance of studies involving autophagy and apoptosis during pre-clinical studies of new drugs with anticancer properties. (C) 2011 Elsevier B. V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/34704
ISSN: 0014-2999
Other Identifiers: http://dx.doi.org/10.1016/j.ejphar.2011.12.031
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