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作 者:王伟迪[1] 徐维平[1,2] 魏伟[1] 路景涛[1] 王杰[1] 周冉[1] 黄莺[1] 魏浩洁[1]
机构地区:[1]安徽医科大学临床药理研究所,省部共建抗炎免疫重点实验室,安徽省中药研究与开发重点研究室,抗炎免疫药物工程技术研究中心,合肥230032 [2]安徽医科大学附属省立医院,合肥230001
出 处:《中国新药杂志》2011年第14期1334-1340,共7页Chinese Journal of New Drugs
摘 要:目的:观察与相同剂量的单药相比,褪黑素(MT)与酵母硒(Se)联合应用是否能提高对肿瘤的治疗效果及其机制。方法:将S180肉瘤细胞接种于小鼠右腋皮下,分为7组:模型组、Se 100μg.kg-1组、Se200μg.kg-1组、MT40 mg.kg-1组、MT80 mg.kg-1组、Se 100μg.kg-1+MT40 mg.kg-1组、环磷酰胺(CTX)组。10 d后处死小鼠。测定肿瘤组织内细胞周期蛋白依赖性激酶2(CDK2)和p53的表达水平。结果:MT与Se联合应用可显著提高抑瘤率,降低肿瘤重量,降低CDK2的表达水平,提高p53和p21的表达水平。结论:与相同剂量的单药治疗肿瘤相比,MT与Se两者联合应用能明显提高疗效。Objective: To determine whether the antitumor effect of melatonin(MT) combined with selenium(Se) is superior to the same dose of MT or Se alone,and its mechanism.Methods: S180 sarcoma cells were inoculated subcutaneously on the right axilla of male mice.The mice were randomized into 7 groups,and treated with Se 100 and 200 μg·kg-1,MT 40 and 80 mg·kg-1,Se 100 μg·kg-1+MT 40 mg·kg-1,or cyclophosphamide(CTX).At 10 days after inoculation,the mice were euthanized.The expression of cyclin-dependent kinase 2(CDK2) and p53 in tumor tissues was detected.Results: Both Se and MT reduced the growth of S180 sarcoma cells.Their antitumor effects were mediated via decreasing CDK2 expression and increasing the expression of wild-type p53.The effect of MT combined with Se was more evident.Conclusion: MT and Se are promising drugs for tumor treatment,and their combination can potentiate the efficacy.
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