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机构地区:[1]河南医科大学一附院肿瘤科 [2]河南医科大学二附院肿瘤科
出 处:《实用癌症杂志》1999年第3期171-173,共3页The Practical Journal of Cancer
摘 要:为探讨甲氰咪呱(CIM)对鼠体内IL2/LAK抗肿瘤作用的影响,将B16细胞经尾静脉接种于C57BL/6小鼠,第3d分别应用DHanks液、CIM(10mg/ml)+CIM(1μg/ml)诱导的脾细胞,IL2+IL2(500U/ml)诱导的LAK细胞,CIM(10mg/ml)+IL2+CIM(1μg/ml)和IL2(500U/ml)共同诱导的LAK细胞,观察鼠肺转移结节和生存期。结果显示,单用CIM并不能减少肺转移结节和延长生存期;CIM+IL2/LAK治疗组与IL2/LAK治疗组相比,可减少肺转移结节(P<0.05)和显著延长生存期(P<0.01)。结果表明,CIM能够增强IL2/LAK抗肿瘤作用,可用于治疗肿瘤。To investigate the influence of cimetidine(CIM) on IL 2/LAK antitumor effects of mice in vivo,C57BL/6 mice were injected intravenously with B16 cells and on the third day treated with:D Hanks;CIM(10 mg/ml)+splenocytes induced by CIM(1 μg/ml)(CIM);IL 2+syngeneic LAK cell induced by IL 2(500 U/ml)(IL 2/LAK);CIM(10 mg/ml)+IL 2+syngeneic LAK cell induced by CIM(1 μg/ml) and IL 2(500 U/ml)(CIM+IL 2/LAK) respectively.The number of pulmonary metastases was counted and survival time was observed.Results:The number of pulmonary metastases of mice was not reduced and survival time was not prolonged by CIM alone(both P >0.05);The number of pulmonary metastases of mice was reduced( P <0.05) and survival time was significantly prolonged( P <0.01) by CIM+IL 2/LAK compared with IL 2/LAK alone.Results indicated that CIM could augment antitumor effects of IL 2/LAK.
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