Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/29087
Title: Biphosphinic palladacycle complex mediates lysosomal-membrane permeabilization and cell death in K562 leukaemia cells
Authors: Barbosa, Christiano M. V.
Oliveira, Carlos R.
Nascimento, Fabio D.
Smith, Mickaela C. M.
Fausto, Damela M.
Soufen, Marco Antonio
Sena, Eliana
Araujo, Ronaldo C.
Tersariol, Ivarne L. S.
Bincoletto, Claudia
Caires, Antonio C. F.
UMC
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual de Campinas (UNICAMP)
Keywords: palladacycle
K562
Bcl-2/Bax
apoptosis
lysosomes
acridine orange
Issue Date: 7-Aug-2006
Publisher: Elsevier B.V.
Citation: European Journal of Pharmacology. Amsterdam: Elsevier B.V., v. 542, n. 1-3, p. 37-47, 2006.
Abstract: The cell death mechanism of cytotoxicity induced by the Biphosphinic Palladacycle Complex (BPC) was studied using a K562 leukaemia cell line. the IC50 values obtained for K562 cells post-72 h of BPC were less than 5.0 mu M by using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) and trypan blue assays. Using the Acridine Orange vital staining combining fluorescence microscopy it was observed that the complex triggers apoptosis in K562 cells, inducing DNA fragmentation, as analysed through electrophoresis. Lysosomal-membrane permeabilization was also observed in K562 cells post-5 h of BPC, which suggests intralysossomal accumulation by proton-trapping, since its pK(a) value ranged from 5.1 to 6.5. Caspase-3, and -6 activity induced by BPC in K562 cells was prevented by the cathepsin-B inhibitor [N-(L-3-transpropylcarbamoyl-oxirane-2-carbonyl)-L-isoleucyl-L-proline] (CA074). These events occurred in the presence of endogenous bcl-2 and bax expression. Acute toxicological studies demonstrated that BPC produces no lesions for liver and kidney fourteen-days after drug administration (100 mg/kg - i.p.). White and red blood cells of BPC-treated mice presented normal morphological characteristics. Taken together, these data suggest a novel lysosomal pathway for BPC-induced apoptosis, in which lysosomes are the primary target and cathepsin B acts as death mediator. (c) 2006 Elsevier B.V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/29087
ISSN: 0014-2999
Other Identifiers: http://dx.doi.org/10.1016/j.ejphar.2006.06.004
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