14,15-Epoxyeicosatrienoic acid induces the proliferation and anti-apoptosis of human carcinoma cell

被引:0
|
作者
Zhang, Z. [1 ]
Hu, D. [2 ,3 ]
Zhou, M. G. [1 ]
Liu, H. X. [1 ]
Wu, J. [1 ]
Huang, S. [1 ]
Wang, D. W. [2 ,3 ]
Cai, L. [1 ]
机构
[1] Third Peoples Hosp Chengdu, Inst Cardiovasc Dis Chengdu, Chengdu, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Internal Med, Wuhan 430074, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Gene Therapy Ctr, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Peroxisome proliferator-activated receptor gamma; Expression; Signaling pathways; ACTIVATED PROTEIN-KINASE; PPAR-GAMMA; EPOXYEICOSATRIENOIC ACIDS; CYTOCHROME-P450; 2J2; SIGNALING PATHWAYS; RECEPTOR-GAMMA; GROWTH; PROMOTES; DISEASES; LIGANDS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and the purpose of the study: Epoxyeicosatrienoic acids (EETs), which are cytochrome P450 epoxygenase metabolites of arachidonic acid, have anti-inflammatory effects, modulate smooth muscle proliferation, and inhibit smooth muscle migration. This study was designed to determine whether exogenous EETs have any effect on the cell proliferation and apoptosis of carcinoma cell as well as the possible signaling pathways of EETs in this regulation. Methods: The effects of EETs on the proliferation and anti-apoptosis of human carcinoma cells were measured by MTT assay and flowcytometric analysis, and the regulation of PPAR gamma, epithelial growth factor receptor (EGFR), extracellular signal-regulated kinase (ERK), phosphatidylinositol 3 (PI3)-Kinase/AKT pathways was investigated by reverse transcriptase polymerase chain reaction (RT-PCR) and western blot analysis. Results: Results of this study suggested that 14, 15-EET may activate the expression of PPAR gamma in Tca-8113 cells. 14,15-EET may stimulate cell proliferation, and increase the percentage of cells during S-G2-M phase in Tca-8113 cells significantly. The levels of EGFR, ERK, and PI3 kinase/AKT proteins were significantly induced by treatment of 14, 15-EET and 14,15-EET/AUDA, but no significant changes were observed by addition of GW9662. Conclusion: These findings suggest that exogenous 14,15-EET has potent inhibitory effect on proliferation, and could induce apoptosis in Tca-8113 cell, and these changes are related to the expression of PPAR gamma, the activation of EGFR, ERK, and PI3 kinase/AKT proteins.
引用
收藏
页码:462 / 468
页数:7
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