Proteomics-based identification of proteins with altered expression induced by 12-O-tetradecanoylphorbol 13-acetate in nasopharyngeal carcinoma CNE2 cells

被引:12
|
作者
Jiang, PZ
Gan, M
Huang, H
Shen, XM
Wang, S
Yao, KT [1 ]
机构
[1] So Med Univ, Inst Canc Res, Guangzhou 510515, Peoples R China
[2] So Med Univ, Dept Histol & Embryol, Guangzhou 510515, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Med Coll, Dept Parasitol, Guangzhou 510080, Peoples R China
关键词
12-O-tetradecanoyl-phorbol-13-acetate; nasopharyngeal carcinoma; proteomics; apoptosis;
D O I
10.1111/j.1745-7270.2005.00016.x
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
Nasopharyngeal carcinoma (NPC) is a malignancy with high incidence in Southern China and South-East Asia. Etiology studies indicate that chemical carcinogen promoters, such as 12-O-tetradecanoylphorbol- 13-acetate (TPA), are important factors causing NPC development. However, the mechanism of the TPA effect on NPC remains unclear. In the present study, cells from a poorly differentiated squamous cell carcinoma NPC cell line, CNE2, were stimulated by TPA and proteomics technology was carried out to find protein discrepancies between control and TPA-treated cells. Results revealed that TPA treatment in CNE2 cells could upregulate the expression of "triosephosphate isomerase" and "14-3-3 protein sigma" and downregulate the expression of "reticulocalbin I precursor", "nucleophosmin", "mitochondrial matrix protein p I precursor", and "stathmin". The changes in the expression of these genes suggested that TPA induced CNE2 cells to antiproliferation and to apoptosis, which was confirmed by subsequent apoptosis detection. Therefore, the effects of TPA on nasopharyngeal carcinoma cells were distinct from the effects on primary epithelial cells and we suggest reasons for these differences.
引用
收藏
页码:97 / 106
页数:10
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