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Apoptosis induction and cell cycle perturbation in established cell lines by peroxysomicine A1 (T-514).
Martinez, F J; Zeng, G Q; Piñeyro, A; Garza-Ocañas, L; Tomei, L D; Umansky, S R.
Afiliación
  • Martinez FJ; School of Medicine, Departments of Pharmacology and Toxicology and Internal Medicine, Universidad Autónoma de Nuevo León, Ave. Gonzalitos #235 Norte, Monterrey 64460, N.L., Mexico. frmartin@ccr.dsi.uanl.mx
Drug Chem Toxicol ; 24(3): 287-99, 2001 Aug.
Article en En | MEDLINE | ID: mdl-11452400
Peroxysomicine A1, a novel potential anticancer compound induced cell death in established cell lines and in a primary culture of rat neonatal cardiomyocytes. Non-transformed cells are less sensitive to the compound than transformed cell lines. Fluorescent microscopy of dying cells stained with DNA-specific dyes revealed chromatin condensation and nuclear fragmentation as well as membrane blebbing characteristic of apoptosis. Flow cytometry of cells treated with peroxysomicine A1, demonstrated appearance of cells containing less than 2C DNA, that indicated degradation of nuclear DNA, another hallmark of apoptotic cell death. Z-VAD, a nonspecific caspase inhibitor, prevented DNA fragmentation but not cell death registered by permeabilization of cell outer membrane. Peroxysomicine A1 also inhibited proliferation of various cell lines. Flow cytometry analysis showed significant accumulation of dividing cells in G2/M phases of cell cycle indicating, most likely delay in G2. These results provide initial insight into the mechanisms of action of peroxysomicine A1 and suggest that peroxysomicine A1 is a potent inhibitor of cell proliferation and inducer of apoptosis and may be a useful antineoplastic chemotherapeutic agent.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentación del ADN / Antracenos / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Revista: Drug Chem Toxicol Año: 2001 Tipo del documento: Article País de afiliación: México Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentación del ADN / Antracenos / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Revista: Drug Chem Toxicol Año: 2001 Tipo del documento: Article País de afiliación: México Pais de publicación: Estados Unidos