SUPPRESSION OF BCL-2 MESSENGER-RNA PRODUCTION MAY MEDIATE APOPTOSIS AFTER IONIZING-RADIATION, TUMOR-NECROSIS-FACTOR-ALPHA, AND CERAMIDE

被引:0
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作者
CHEN, M
QUINTANS, J
FUKS, Z
THOMPSON, C
KUFE, DW
WEICHSELBAUM, RR
机构
[1] UNIV CHICAGO,DEPT RADIAT & CELLULAR ONCOL,CHICAGO,IL 60637
[2] UNIV CHICAGO,DEPT PATHOL,COMM IMMUNOL,CHICAGO,IL 60637
[3] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
[4] UNIV CHICAGO,HOWARD HUGHES MED INST,CHICAGO,IL 60637
[5] MEM SLOAN KETTERING CANC CTR,DEPT RADIAT THERAPY,NEW YORK,NY 10021
[6] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,PHARMACOL LAB,BOSTON,MA 02115
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D O I
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent studies have proposed that tumor necrosis factor alpha (TNF-alpha) and ionizing radiation induce apoptosis by activating hydrolysis of sphingomyelin to ceramide, Bcl-2 and a related gene, Bcl-X, inhibit several forms of apoptosis, Herein, we report that internucleosomal DNA fragmentation, characteristic of apoptosis and induced by ionizing radiation, is accompanied by concomitant decreases in Bcl-2 and Bcl-X mRNA levels in HL-60 and U-937 human leukemia cells. Apoptotic DNA fragmentation after exposure to TNF-alpha and C-2-ceramide was also associated with down-regulation of Bcl-2 mRNA in HL-60 and U-937 cells, while Bcl-X mRNA production was unaffected, These results suggest that modulation of Bcl-2 gene expression may be a target for ceramide-mediated apoptosis following exposure to ionizing radiation and TNF-alpha. Changes in Bcl-2 expression may be the basis for the interactive killing observed between radiation and TNF-alpha in some human and tumor cells.
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页码:991 / 994
页数:4
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