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丝裂霉素C与C2-神经酰胺或抗Fas单克隆抗体联合治疗膀胱癌的体外研究
引用本文:时京,孔垂泽,王侠,杨绍波,刘奔,孙志熙,杜君. 丝裂霉素C与C2-神经酰胺或抗Fas单克隆抗体联合治疗膀胱癌的体外研究[J]. 中国医科大学学报, 2007, 36(1): 41-43,46
作者姓名:时京  孔垂泽  王侠  杨绍波  刘奔  孙志熙  杜君
作者单位:中国医科大学附属第一医院泌尿外科,辽宁,沈阳,110001
摘    要:目的:探讨丝裂霉素C(MMC)与C2-神经酰胺(C2-Cer)或抗Fas单克隆抗体(anti-FasmAb)联合应用对人膀胱癌BIU-87和T24细胞生长的抑制作用。方法:采用四甲基偶氮唑蓝(MTT)比色法测定MMC、C2-Cer、anti-FasmAb单独应用及MMC分别与C2-Cer或anti-FasmAb联合应用对人膀胱癌BIU-87和T24细胞生长的抑制作用,并应用CHOU-TALALAY联合指数法对药物联合应用的效果进行判定。结果:药物单用及MMC分别与C2-Cer、anti-FasmAb合用对BIU-87和T24细胞的生长均有抑制作用,药物合用时的中效浓度与单用时比较有不同程度的降低。MMC与C2-Cer合用时,对于BIU-87细胞,表现为协同作用(CI<1);对于T24细胞,低浓度(0%1)。MMC与anti-FasmAb合用时,对于BIU-87细胞,在大部分效应范围(18%1);对于T24细胞,则在大部分效应范围(0
关 键 词:膀胱肿瘤    药物治疗  联合
文章编号:0258-4646(2007)01-0041-03
修稿时间:2005-12-21

Effect of mitomycin C combined with C2-ceramide or anti-Fas monoclonal antibody in human bladder cancer cells
SHI Jing,KONG Chui-ze,WANG Xia,YANG Shao-bo,LIU Ben,SUN Zhi-xi,DU Jun. Effect of mitomycin C combined with C2-ceramide or anti-Fas monoclonal antibody in human bladder cancer cells[J]. Journal of China Medical University, 2007, 36(1): 41-43,46
Authors:SHI Jing  KONG Chui-ze  WANG Xia  YANG Shao-bo  LIU Ben  SUN Zhi-xi  DU Jun
Affiliation:Department of Urological Surgery,The Fast Affiliated Hospital, China Medical University, Shenyang 10001, China
Abstract:Objective:To study the anti-cancer effect of mitomycin C (MMC) combined with C2-ceramide (C2-Cer) or anti-Fas monoclonal antibody (anti-Fas mAb) in human bladder cancer cell lines BIU-87 and T24. Methods:The inhibitory effects of MMC,C2-Cer,anti-Fas mAb,and MMC combined with C2-Cer or anti-Fas mAb on BIU-87 and T24 cells were determined by MTT assay,and the effect of the combination therapy was evaluated by combination-index method of CHOU and TALALAY. Results:The inhibitory effect was found when these 3 drugs were used alone or together. The median effect concentrations of these 3 drugs decreased to various extents when the drugs were used together. MMC was synergistic with C2-Cer in BIU-87 cells. In T24 cells,low concentration of MMC was synergistic with low concentration of C2-Cer,and high concentration of MMC was antagonistic to high concentration of C2-Cer. In the majority of effect range,MMC was antagonistic to anti-Fas mAb in BIU-87 cells and synergistic with anti-Fas mAb in T24 cells. Conclusion:The effects of combination therapy are different in different bladder cancer cell lines. The concentrations of anticancer drugs may decrease in the combination therapy.
Keywords:bladder cancer  drug therapy  combination
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