## Background: Inhibition of apoptosis, or programmed cell death, may be critical both in the development of cancer and in determining response to therapy. the authors examined the expression of two related apoptotic inhibitors, bcl-2 and bcl-xl, in pretreatment biopsies from a series of 42 patient
Over-expression of bcl-xL gene in human gastric adenomas and carcinomas
β Scribed by Shinya Kondo; Yasuhisa Shinomura; Shuji Kanayama; Yoshifumi Higashimoto; Jun-Ichiro Miyagawa; Takeshi Minami; Tatsuya Kiyohara; Shinichiro Zushi; Shinji Kitamura; Koji Isozaki; Yuji Matsuzawa
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 543 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
The present study was designed to clarify whether bcl-xL is involved in the development of carcinoma in the stomach. Levels of bcl-xL and bcl-2 mRNA were determined by a reverse-transcription/polymerase-chain reaction in endoscopic gastric biopsy specimens from 10 control subjects, 11 patients with adenomas and 14 patients with carcinomas. In 6 of 11 adenomas, 5 of 8 early carcinomas and 3 of 6 advanced carcinomas, the bcl-xL gene was over-expressed. In carcinomas, over-expression of the bcl-xL gene was observed in 6 of 9 intestinal-type carcinomas and 2 of 5 diffuse-type carcinomas. No correlation was observed between bcl-xL and bcl-2 gene expression. In cases in which the bcl-xL gene was over-expressed, an apparent increase in the protein level of Bcl-xL was observed by immunoblot analysis and intense Bcl-x immunoreactivity was detected immunohistochemically within the tumor cells. In conclusion, we showed that bcl-xL is over-expressed in gastric carcinomas at both the RNA and protein levels, suggesting that over-expression of bcl-xL may play a role in gastric carcinogenesis.
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