东南大学学报(医学版)
東南大學學報(醫學版)
동남대학학보(의학판)
JOURNAL OF NANJING RAILWAY MEDICAL COLLEGE
2002年
1期
16-19,23
,共5页
余卫平%王国桢%高蕾%卫开斌%沈成兴
餘衛平%王國楨%高蕾%衛開斌%瀋成興
여위평%왕국정%고뢰%위개빈%침성흥
肝细胞生长因子%肝细胞癌%细胞周期
肝細胞生長因子%肝細胞癌%細胞週期
간세포생장인자%간세포암%세포주기
hepatocyte growth factor%hepatocellular carcinoma%cell cycle%in vitro
目的:观察肝细胞生长因子(HGF)对体外培养的人肝细胞癌细胞的生长效应.方法:将处于指数生长期的SMMC-7721细胞经过(HGF处理组)或不经(对照组)HGF处理培养1~4d,采用四甲基偶氮唑盐(MTT)法检测细胞数,并进行细胞周期分析.结果:HGF对SMMC-7721细胞增殖具有剂量依赖性抑制作用.在实验浓度内,使用最高浓度的HGF(rhHGF为20μg*L-1、cHGF为100mg*L-1)对细胞增殖抑制作用最强.使用不同浓度(5、10、20μg*L-1)rhHGF处理3d的培养细胞均有一半以上停留在G0/G1期.结论:HGF对SMMC-7721人肝细胞癌细胞的体外生长有强烈的抑制作用,这与细胞生长阻滞在G0/G1期有关.
目的:觀察肝細胞生長因子(HGF)對體外培養的人肝細胞癌細胞的生長效應.方法:將處于指數生長期的SMMC-7721細胞經過(HGF處理組)或不經(對照組)HGF處理培養1~4d,採用四甲基偶氮唑鹽(MTT)法檢測細胞數,併進行細胞週期分析.結果:HGF對SMMC-7721細胞增殖具有劑量依賴性抑製作用.在實驗濃度內,使用最高濃度的HGF(rhHGF為20μg*L-1、cHGF為100mg*L-1)對細胞增殖抑製作用最彊.使用不同濃度(5、10、20μg*L-1)rhHGF處理3d的培養細胞均有一半以上停留在G0/G1期.結論:HGF對SMMC-7721人肝細胞癌細胞的體外生長有彊烈的抑製作用,這與細胞生長阻滯在G0/G1期有關.
목적:관찰간세포생장인자(HGF)대체외배양적인간세포암세포적생장효응.방법:장처우지수생장기적SMMC-7721세포경과(HGF처리조)혹불경(대조조)HGF처리배양1~4d,채용사갑기우담서염(MTT)법검측세포수,병진행세포주기분석.결과:HGF대SMMC-7721세포증식구유제량의뢰성억제작용.재실험농도내,사용최고농도적HGF(rhHGF위20μg*L-1、cHGF위100mg*L-1)대세포증식억제작용최강.사용불동농도(5、10、20μg*L-1)rhHGF처리3d적배양세포균유일반이상정류재G0/G1기.결론:HGF대SMMC-7721인간세포암세포적체외생장유강렬적억제작용,저여세포생장조체재G0/G1기유관.
Objective To make sure whether hepatocyte growth factor(HGF) is a negative growth regulator for human hepatocellular carcinoma(HCC) cells or not,we observed the growth effects of both recombinant human HGF(rhHGF) and native calf HGF(cHGF) on SMMC-7721 human HCC cell line,which was derived from the hepatocarcinoma tissue of a Chinese HCC patient.Methods SMMC-7721 human HCC cells were cultured to the exponential phase of growth and then treated with(HGF-treated group)or without(control) rhHGF/cHGF.After 1~4 d,the number of viable cells was determined by a photometric method using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT). The cells incubated with rhHGF were subjected to analysis of cell cycle distribution by flow cytometric assay.Results A similar type of dose-dependent cell growth inhibition effect on SMMC-7721 human HCC cells by rhHGF(5~20μg*L-1) as well as by cHGF(25~100mg*L-1) has been found, with the maximal effect seen at the highest concentration used. Approximately over 50% of the cells treated with rhHGF(5μg*L-1,10μg*L-1,20μg*L-1) accumulated in the quiescent G0/G1 phase of the cell cycle over incubation period for 3d.Conclusion The growth of SMMC-7721 human HCC cells is strongly inhibited by rhHGF or cHGF.The cells exposed to HGF are arrested in the G0/G1 phase of the cell cycle.Thus,our study prove that HGF may be a negative growth regulator for human HCC cells.