检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]河北联合大学附属医院妇科,河北唐山063000
出 处:《实用药物与临床》2014年第9期1096-1099,共4页Practical Pharmacy and Clinical Remedies
摘 要:目的探讨靶向治疗药物甲磺酸伊马替尼(Imatinib mesylate)对耐顺铂人卵巢腺癌细胞株SKOV3/DDP的增殖抑制和诱导凋亡作用以及与顺铂合用的效果。方法 MTT法检测不同浓度甲磺酸伊马替尼、DDP以及联合用药对人卵巢癌耐顺铂细胞株SKOV3/DDP的增殖抑制情况,采用双染色流式细胞术检测甲磺酸伊马替尼对SKOV3/DDP的诱导凋亡作用。结果 MTT法检测出不同药物浓度的甲磺酸伊马替尼作用于SKOV3/DDP细胞呈现细胞生长抑制作用,甲磺酸伊马替尼与不同浓度顺铂联合用药对细胞生长抑制率分别为38.63%、51.55%、66.54%,明显高于DDP单用药组的8.30%、16.68%、30.83%,两组比较差异有统计学意义(P<0.05)。两药合用后的IC50为9.57,是单用顺铂组的4.13倍。甲磺酸伊马替尼与顺铂合用后,早期凋亡率由1.25%增加到12.31%(P<0.05)。结论甲磺酸伊马替尼可以抑制卵巢癌耐DDP细胞株SKOV3/DDP的增殖和诱导细胞凋亡,并显著增强其对DDP的敏感性。Objective To study the effects of imatinib mesylate on proliferation,apoptosis and cell resistance of drug-resistant ovarian cancer cell line SKOV3/DDP.Methods MTT assay was used to examine the inhibition effect of different concentrations of imatinib mesylate,DDP and combination drugs use on proliferation of ovarian cancer cell line SKOV3/DDP,and flow cytometry was used to detect the apoptosis of SKOV3/DDP induced by imatinib mesylate.Results MTT showed that different concentrations of imatinib mesylate in SKOV3/DDP cells had inhibition effect.The inhibition rates of imatinib mesylate and cisplatin combination in different concentrations were 38.63%,51.55 %,66.54 %,which were significantly higher than those for DDP (8.30%,16.68 %,30.83 %),there were signifi cant differences between the two groups(P < 0.05).IC50 of combination was 9.57,which was 4.13 times for that of cisplatin alone.When cisplatin was used combination with imatinib mesylate,early apoptosis rate increased from 1.25 %to 12.31% (P < 0.05).Conclusion Imatinib mesylate can inhibit DDP resistant ovarian cancer cell lines SKOV3/ DDP proliferation and induce cell apoptosis,and significantly enhance its sensitivity to the DDP.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.190.219.46