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作 者:刘芳[1] 刘杰 张华[1] 于雁[1] 钱路静[3] 尚丽华[1] 胡静[1] 车德海[1]
机构地区:[1]哈尔滨医科大学附属第三医院肿瘤内六科,哈尔滨150081 [2]鹤岗矿务局有限责任公司总医院消化内科 [3]厦门市第三医院
出 处:《实用肿瘤学杂志》2013年第1期42-45,共4页Practical Oncology Journal
基 金:黑龙江省教育厅科学技术研究资助项目(11541248)
摘 要:目的探讨不同序贯的阿妥昔单抗(Cetuximab,C225)与化疗药物联合对人胃腺癌细胞株SGC-7901的增殖抑制作用,寻找治疗胃癌的新方法、新配方。方法选用浓度递增的Cetuximab和化疗药物奥沙利铂、氟尿嘧啶、卡培他滨,分别按照不同给药方式单药、序贯作用于SGC-790l细胞,采用细胞计数试剂盒检测不同给药方式对SGC-7901细胞的增殖抑制作用,计算不同序贯给药时Cetuximab和化疗药物的半数抑制浓度(1C50)的变化,及其l卡}I瓦作川的协同系数(CI)。结果Cetuximab和化疗药物联用对SGC-7901细胞的增殖抑制作用受给药序贯影响:Cetuximab先于化疗药物给药,两者的IC50较单用时降低,但cI值均大于l,两者之间为拈抗效应;Cetuximab后于化疗药物给药,两者的IC50较单川时降低更为明显,且cI值均小于1,两者之间具有较明品的协同效应。结论Cetuximab联合化疔药物对胃癌细胞SGC-7901的增殖具有协同抑制作用,化疗药物先于Cetuximab的序贯给药方式能获得明显的协同效应。Objective To evaluate inhibition effecton proliferation of SCG -7901 cell in different se- quences comlfination of Cetuximab with either oxaliplafin, funaioniding or Capeeitabine. To explore the optimal treatmenl schedule of combination of Cetuximab and eytotoxic drngs. Methods Increasing concentration of Celuximab(5 -500 rag/L)eombined with increasing concentration cytotoxic drugs was administrated to human gaslrie cancer cell lines SCG- 7901 with different sequences. The prolilbration inhihition eftet on SCG -7901 cell was detected with CCK -8 assay. The IC50 and CIef Cetuximab and either eytotoxie drugs were eahulated. Results The eombinalion of a eytotoxie drug with Celuximab caused differeul antiproliferatiw effees on SCG - 7901 cells depending on diflerenl treatment sequenees. The respective 1C50 nf Cet/iximab and eytotoxie drugs decreased when (eluxima) followed by chemotherapy,while the CI values were all 〉 I , which indicated an antagonistic interaction. In eonlrasl, wh chemotherapy was tllowed by Cetuximab, the respective50 of drugs decreased more remarkably aud lhe (21 wl.lues were all 〈 I ,which indicated a signitieanl synergistic auliprolib,raliwlivily and conduce to less doses and mihler side effecls in cliuical application.
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