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胡关胜  范学工  周蓉蓉  王志明 《肝脏》2011,16(2):109-112
目的 研究晚期糖基化终产物受体(RAGE)在原发性肝细胞癌(PHC)中的表达.方法 收集10例PHC患者的肝癌组织、癌旁组织、血清及正常人的血清;用RT-PCR及Western blot分别检测组织中RAGE基因及蛋白的表达;用ELISA检测血清RAGE表达,同时用化学发光法检测血清中甲胎蛋白(AFP)表达.结果 RA...  相似文献   
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The aim of this study was to investigate the effect of Paris saponinⅠ(PSⅠ)on human gas-tric carcinoma cell growth and apoptosis and to explore the potential mechanisms.The proliferation of SGC7901 cells was monitored by the MTT cell viability assay,while the nuclear morphology of apoptotic cells was assessed by Hoechst 33258 staining.Flow cytometry was performed to analyze the cell cycle progression of propidium iodide(PI)-stained SGC7901 cells and the apoptotic rate of annex-inⅤ/PI-stained cells.Western blotting was used to examine the expression of several cell cycle proteins,including cyclin B1 and Cdk1,and the apoptosis-regulated proteins Bcl-2,Bax,cytochrome c,procas-pase-9,and procaspase-3.The MTT assay demonstrated that PSⅠ could induce significant dose-and time-dependent inhibition of SGC7901 cell proliferation.Marked morphological changes,including condensation of chromatin,nuclear fragmentation and apoptotic bodies were clearly shown on Hoechst 33258 staining.PSⅠ treatment also resulted in the disruption of the cell cycle at G2/M and the induction of apoptosis.Following PSⅠ treatment,the cell cycle-related proteins cyclin B1 and Cdk1 were down-regulated.Expression of the pro-apoptotic protein Bax was increased,while anti-apoptotic protein Bcl-2 decreased.PSⅠ treatment resulted in elevated cytoplasmic cytochrome c and activation of the apoptotic proteases caspase-9 and caspase-3.These data indicate that PSⅠ acts as an inhibitor of proliferation in SGC7901 cells by inducing cell cycle arrest and mitochondria-dependent apoptosis.PSⅠ is a potential therapeutic agent against human gastric carcinoma.  相似文献   
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