摘要: |
[目的]探讨伊立替康(CPT-11)及联合5-氟尿嘧啶(5-FU)、顺铂(DDP)对人肝癌细胞株的细胞毒性作用。[方法]利用MTT比色法检测CPT-11,5-FU,DDP 3种药物对人肝癌HepG2细胞株的抑制率,进一步测定3种药物单药及联合用药对细胞生长抑制的情况并进行比较。[结果]不同浓度CPT-11,5-FU,DDP作用细胞后,细胞生长受到不同程度的抑制,这一抑制作用随药物浓度的升高而增强(P<0.01), 单药对肝癌细胞株抑制作用最强的为CPT-11,其次为DDP,5-FU(三药作用于相同起始浓度的肝癌细胞株48、72、96、120 h后细胞数量分别为 4.70±0.25、12.71±0.23、20.30±1.59、24.20±2.31;6.50±0.81、16.25±0.72、24.60±0.65、31.30±2.31;9.50±0.06、17.75±0.19、30.00±0.41、38.40±1.01;单位为1×104 个/孔,与对照组比较P<0.01)。联合用药时抑制作用最强的为CPT-11、DDP、5-FU联合用药组,后依次为CPT-11、DDP联合、CPT-11、
5-FU联合、5-FU、DDP联合(四组药物作用于相同起始浓度的肝癌细胞株48、72、96、120 h后细胞数量分别为6.30±0.79、9.50±0.66、14.50±0.03、21.40±0.66;6.60±0.54、12.20±0.71、20.90±0.45、28.80±0.36;9.00±0.61、16.40±0.29、30.40±0.37、37.30±0.25;12.00±0.02、18.80±0.39、30.70±0.07、35.40±0.08;单位为1×104 个/孔,与对照组比较P<0.01)。[结论]CPT-11对肝癌细胞株具有一定的细胞毒性作用,并强于目前肝癌临床常规用药5-FU、DDP,CPT-11可与DDP、5-FU联合应用于原发性肝癌的治疗。 |
关键词: 伊立替康 5-氟尿嘧啶 顺铂 原发性肝癌 HepG2细胞株 |
DOI:10.11724/jdmu.2008.02.09 |
分类号:R73-3 |
基金项目: |
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Experimental study of cytotoxicity of CPT-11 and combinated with 5-FU and DDP on human hepatocellular carcinoma strain |
LIU Fang1, ZHANG Yang1, SHAO Shu-juan2, ZHOU Jin-ping1, ZHAO Jin-bo1
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1.Department of Oncology, the Second Affiliated Hospital of Dalian Medical University, Dalian 116027, China;2.Department of Histology and Embryology,Dalian Medical University, Dalian 116044,China
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Abstract: |
[Objective]This study explore the cytotoxic effect of CPT-11 and combinated with 5-FU and DDP on hepatocellular carcinoma strain.[Methods]To detect the depression rate of CPT-11,5-FU and DDP on human hepatocellular carcinoma HepG2 strain respectively though MTT colorimetric method and to determine further the depression rate of combination of three drugs to contract.[Results]The growth of cell was depressed at various levels by sequential concentration of CPT-11,5-FU and DDP , and the effect promote with increasement of concentration; the depression effect of CPT-11 was most great in the three drugs, the more was DDP, and the last was 5-FU(the respective cell quantities of CPT-11 and DDP and 5-FU on human hepatocellular carcinoma strain with equal initial concentration after 48,72,96,120 h was 4.70±0.25,12.71±0.23,20.30±1.59,24.20±2.31;6.50±0.81,16.25±0.72,24.60±0.65,31.30±2.31;9.50±0.06,17.75±0.19,30.00±0.41,38.40±1.01;1×104/ hole,contrast with control group P<0.01), while combination with three drugs depress most strongly cell growth in various drugs combination, the more is CPT-11 and DDP,CPT-11 and 5-FU, the last was 5-FU and DDP (the respective cell quantities of four groups on human hepatocellular carcinoma strain with equal initial concentration after 48,72,96,120 h was:6.30±0.79,9.50±0.66,14.50±0.03,21.40±0.66;6.60±0.54,12.20±0.71,20.90±0.45,28.80±0.36;9.00±0.61,16.40±0.29,30.40±0.37,37.30±0.25;12.00±0.02,18.80±0.39,30.70±0.07,35.40±0.08;1×104/ hole,contrast with control group P<0.01).[Conclusion]There is considerable effect of CPT-11 on hepatocellular carcinoma strain. It is more obvious than 5-FU and DDP, which are used commonly in clinic. The strong depression of combination with three drugs provide theoretic foundation for clinical combination therapy. |
Key words: hepatocellular carcinoma Irinotecan HepG2 cell strain 5-FU DDP |