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Troglitazone, a peroxisome proliferator-activated receptor γ ligand, induces growth inhibition and apoptosis of HepG2 human liver cancer cells
作者单位:Yan-Ming Zhou(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;Yin-Hao Wen(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;Xiao-Yan Kang(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;Hai-Hua Qian(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;Jia-Mei Yang(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;Zheng-Feng Yin(Department of Molecular Oncoiogy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China) ;
基金项目:Supported by Grants from the State Key Basic Research Program, No. 2002CB513100
摘    要:AIM: To examine the effect of troglitazone, a peroxisome proliferator-activated receptor γ (PPARγ) ligand, on the proliferation and apoptosis of human liver cancer cells. METHODS: Liver cancer cell line HepG2 was cultured and treated with troglitazone. Cell proliferation was detected by 3-(4-,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay; apoptosis was detected by flow cytometry and terminal deoxynucleotidyl transferase- mediated nick end labeling of DNA fragmentation sites (TUNEL) assay; and apoptosis-related protein was detected by immunocytochemistry and Western blotting. RESULTS: Troglitazone inhibited growth and induced apoptosis of HepG2 cells in a dose-dependent manner, and induced activation of caspase-3 expression. Troglitazone not only drove apoptosis-inhibiting factor survivin to translocate incompletely from the nucleus to the cytoplasm, but also inhibited expression of survivin, while it did not affect expression of apoptosis-promoting factor Bax. CONCLUSION: PPARγ ligands inhibit growth and induce apoptosis of liver cancer cells, and may have applications for the prevention and treatment of liver cancer.

关 键 词:肝肿瘤  细胞凋亡  过氧物酶体  治疗方法
收稿时间:2007-09-19

Troglitazone, a peroxisome proliferator-activated receptor �� ligand, induces growth inhibition and apoptosis of HepG2 human liver cancer cells
Yan-Ming Zhou Yin-Hao Wen Xiao-Yan Kang Hai-Hua Qian Jia-Mei Yang Zheng-Feng Yin. Troglitazone, a peroxisome proliferator-activated receptor �� ligand, induces growth inhibition and apoptosis of HepG2 human liver cancer cells[J]. World journal of gastroenterology : WJG, 2008, 14(14): 2168-2173. DOI: 10.3748/wjg.14.2168
Authors:Yan-Ming Zhou Yin-Hao Wen Xiao-Yan Kang Hai-Hua Qian Jia-Mei Yang Zheng-Feng Yin
Affiliation:Department of Molecular Oncology, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China
Abstract:AIM: To examine the effect of troglitazone, a peroxisome proliferator-activated receptor γ (PPARγ) ligand, on the proliferation and apoptosis of human liver cancer cells.METHODS: Liver cancer cell line HepG2 was cultured and treated with troglitazone. Cell proliferation was detected by 3-(4-,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay; apoptosis was detected by flow cytometry and terminal deoxynucleotidyl transferasemediated nick end labeling of DNA fragmentation sites (TUNEL) assay; and apoptosis-related protein was detected by immunocytochemistry and Western blotting.RESULTS: Troglitazone inhibited growth and induced apoptosis of HepG2 cells in a dose-dependent manner,and induced activation of caspase-3 expression.Troglitazone not only drove apoptosis-inhibiting factor survivin to translocate incompletely from the nucleus to the cytoplasm, but also inhibited expression of survivin,while it did not affect expression of apoptosis-promoting factor Bax.CONCLUSION: PPARγ ligands inhibit growth and induce apoptosis of liver cancer cells, and may have applications for the prevention and treatment of liver cancer.
Keywords:Peroxisome proliferator-activated receptor γ  Troglitazone  Liver neoplasms  Apoptosis
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