槟榔碱
槟榔
谷胱甘肽
癌变
化学
c-jun公司
致癌物
分子生物学
癌症研究
生物
生物化学
转录因子
酶
基因
螺母
受体
工程类
结构工程
毒蕈碱乙酰胆碱受体
作者
Tse-Jung Ho,Chun-Pin Chiang,Chi-Yuan Hong,Sang-Heng Kok,Ying-Shiung Kuo,M. Tien Kuo
出处
期刊:Oral Oncology
[Elsevier]
日期:2000-09-01
卷期号:36 (5): 432-436
被引量:23
标识
DOI:10.1016/s1368-8375(00)00031-2
摘要
To investigate the mechanisms of areca quid (AQ)-induced carcinogenesis, expression of c-fos and c-jun protooncogenes was examined in human oral mucosal fibroblasts after exposure to areca nut extracts (ANE) or arecoline. We found that treatment of cells with 200 microg/ml ANE or 10 microg/ml arecoline for 1 h induced about three-fold increase in c-jun mRNA levels. This increase was transient and the level of c-jun mRNAs returned rapidly to control levels thereafter. However, ANE and arecoline did not induce c-fos mRNA expression at detectable levels. During AQ chewing, oral mucosal cells are continuously stimulated by ANE and arecoline. Persistent induction of the c-jun protooncogene by ANE and arecoline may be one of the mechanisms in the carcinogenesis of oral squamous cell carcinoma in Taiwan. Furthermore, we observed that pre-incubation of cells with either N-acetyl-cysteine [a glutathione (GSH) precursor] or L-buthionine-S,R-sulfoximine (a specific inhibitor of GSH biosynthesis) had a minimal effect on arecoline-induced c-jun expression. Therefore, arecoline-induced c-jun expression is independent of GSH depletion.
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