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Evidence for post-transcriptional down-regulation of the apoptosis-related gene bcl-2 in human colorectal cancer
被引:1
|作者:
Berney, CR
Downing, SR
Yang, JL
Russell, PJ
Crowe, PJ
机构:
[1] Univ New S Wales, Prince Wales Hosp, Dept Surg, Randwick, NSW 2031, Australia
[2] Univ New S Wales, Prince Wales Hosp, Oncol Res Ctr, Randwick, NSW 2031, Australia
来源:
关键词:
bcl-2;
colorectal carcinoma;
liver metastasis;
adenoma;
immunohistochemistry;
in situ hybridization;
D O I:
10.1002/(SICI)1096-9896(200005)191:1<15::AID-PATH566>3.0.CO;2-E
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
This retrospective study was undertaken to investigate the expression of bcl-2 protein and messenger RNA in colorectal cancer (CRC). Immunohistochemical analysis using a monoclonal mouse antibody to the bcl-2 protein and in situ hybridization using a digoxigenin-labelled bcl-2 cRNA probe were carried out on formalin-fixed and paraffin-embedded specimens from 53 colorectal adenocarcinomas, 27 liver secondaries, and 60 adenomas with various degrees of dysplasia, Normal human tonsil sections were used as positive controls. Expression of bcl-2 protein and of messenger RNA was evaluated semiquantitatively. The expression of bcl-2 protein was gradually and significantly lost during the progression from moderately dysplastic adenoma to primary CRC (moderate/severe dysplasia: Mann-Whitney U-test, p = 0.0001; severe dysplasia/ primary CRC: p = 0.027), whereas the cellular expression of bcl-2 mRNA was gradually increased during the dysplasia/adenoma-carcinoma neoplastic sequence. These observations suggest that in a proportion of colorectal cancer cases, the bcl-2 proto-oncogene expression may be downregulated at a post-transcriptional level. Copyright (C) 2000 John Wiley & Sons, Ltd.
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页码:15 / 20
页数:6
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