학술논문

Staurosporine-induced apoptosis and hydrogen peroxide-induced necrosis in two human breast cell lines.
Document Type
Journal Article
Source
British Journal of Cancer. 1/13/2003, Vol. 88 Issue 1, p125-131. 7p.
Subject
*APOPTOSIS
*HYDROGEN peroxide
*NECROSIS
*BREAST cancer
*CANCER cell culture
*RESEARCH
*ALKALOIDS
*RESEARCH methodology
*EVALUATION research
*COMPARATIVE studies
*CELL lines
*ENZYME inhibitors
*BREAST tumors
*PHARMACODYNAMICS
Language
ISSN
0007-0920
Abstract
The use of apoptosis-inducing agents in the treatment of malignant cancer is increasingly being considered as a therapeutic approach. In this study, the induction of apoptosis and necrosis was examined in terms of temporal dose responses, comparing a malignant and nonmalignant breast cell line. Staurosporine (SSP)-induced apoptosis and H(2)O(2)-induced necrosis were evaluated by two cytotoxicity assays, neutral red (NR) and methyl-thiazolyl tertrazolium (MTT), in comparison with a differential dye uptake assay, using Hoechst33342/propidium iodide (Hoechst/PI). Confirmatory morphological assessment was also performed by routine resin histology and transmission electron microscopy. Cell viability was assessed over a 0.5-48 h time course. In nonmalignant HBL-100 cells, 50 nM SSP induced 100% apoptosis after a 48 h exposure, while the same exposure to SSP caused only 4% apoptosis in metastatic T47D cells. Although complete apoptosis of both cell lines was induced by 50 microM SSP, this effect was delayed in T47D (24 h) compared with HBL-100 (4 h). Results also showed that neither MTT or NR can distinguish between the modes of cell death, nor detect the early onset of apoptosis revealed by Hoechst/PI. [ABSTRACT FROM AUTHOR]