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作 者:魏育林[1] 赵天德[1] 金思源 曹炜[1] 牛建昭[1] 刘德若[1] 崔振宇 张宜俊 孔祥平
机构地区:[1]中日友好医院临床医学研究所,北京中医药大学,北京地坛医院,空军广州医院
出 处:《上海免疫学杂志》1996年第1期33-36,共4页Shanghai Journal of Immunology
摘 要:本文从细胞学、DNA凝胶电泳、流式细胞术三方面研究促肝细胞生长素(pHGF)在体外对肝癌细胞增殖活性的影响。结果表明:pHGF对肝癌BEL-7402细胞增殖有抑制作用,并存在剂量和时间相关性。其48h的半数抑制浓度(ID50)为0.37mg/ml±0.04mg/ml。而37℃灭活的pHGF对BEL-7402细胞增殖在15h无抑制作用,在24和48h抑制作用很弱(ID50>1.5mg/ml)。DNA凝胶电泳结果表明,pHGF可诱导BEL7402细胞产生细胞凋亡(Apoptosis)。流式细胞术(FCM)结果显示:pHGF抑制BEL-7402细胞增殖过程是先使细胞停留在G0/G1期,继而诱导细胞产生凋亡。后两项结果均显示pHGF对人肝癌细胞凋亡的诱导里时间和剂量相关性。Hepatocyte growth-promoting factor(pHGF), a drug for the treatment of severe and chronic active hepatitisis in China, has been reported to accelerate hepatocyte growth in vitro and in vivo. But effect of pHGF on human hepatocelluar carcinoma cell is unknown. In the present study, we conducted an investigation to determine the anti-tumor effect of pHGF in vitro. The result showed that pHGF suppressed the proliferation of BEL-7402 cells. Inhibitory dose 50(ID50) at 48 hours of exposure to pHGF was 0.37mg/ml±0.04mg/ml. However, almost no suppressive effects were detected at 15 hours of exposure to the heat-inactived pHGF. At 24 hours and 48 hours,the ID50 of the heat-inactived pHGF were > 1.5mg/ml, less than the active pHGF(P<0.05). In agarose gel, DNA fragmentation and ladder form were demonstrated. Cell cycle analysis revealed that at the early period of exposure, pHGF induced arrest of the cells on the G0/G1 phase and at the late period, it induced apoptosis.
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