Differences in expression of pro-caspases in small cell and non-small cell lung carcinoma

被引:68
作者
Joseph, B
Ekedahl, J
Sirzen, F
Lewensohn, R
Zhivotovsky, B
机构
[1] Karolinska Inst, Dept Toxicol, Inst Environm Med, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Unite Med Radiobiol, Canc Ctr Karolinska, S-17176 Stockholm, Sweden
关键词
lung cancer; apoptosis; caspases; Bcl-2; proteins;
D O I
10.1006/bbrc.1999.1191
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of several molecular determinants of apoptosis was analyzed in 10 untreated small cell (SCLC) and 6 untreated non-small cell (NSCLC) lung carcinoma cell lines. Although SCLC lines were more prone to spontaneous apoptosis compared with NSCLC lines, the former showed higher Bcl-2 expression and a higher Bcl-2/Bax ratio. In order to understand this apparent contradiction, the expression of pro-caspases as well as calpain was analyzed in these cell lines at the protein and mRNA levels. No differences in protein level of pro-caspases-2, -3, -7, and -9 and of calpain were detected between the SCLC and the NSCLC lines, but a striking difference in pro-caspase-8 expression was noted. Al 6 NSCLC, but only 2 of the 10 SCLC lines, expressed pro-caspase-8 protein. Further experiments using the RNase protection assay indicated that the lack of pro-caspase-8 expression at the mRNA level was characteristic for SCLC. Using the same experimental approach, we found that SCLC cell lines in addition to pro-caspase-8 were deficient in mRNA expression of pro-caspases-1, -4, and -10, suggesting a different caspase-activating cascade in SCLC compared with NSCLC. This first systematic characterization of pro-caspase expression in lung cancer surprisingly showed that SCLC, which are more prone to undergo spontaneous apoptosis, are deficient in several pro-caspases and have a high Bcl-2/Bax ratio. Thus, the propensity of SCLC cells to undergo apoptosis cannot be explained only by the expression of factors involved in regulation or execution of apoptosis. (C) 1999 Academic Press.
引用
收藏
页码:381 / 387
页数:7
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