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作 者:王薇[1] 邬素芳[1] 许先容[2] 陈刚[1] 徐茜[1] 李辅军[1] 廖国宁[1] 王世宣[1] 周剑峰[1] 卢运萍[1] 马丁[1]
机构地区:[1]华中科技大学同济医学院附属同济医院妇产科,武汉市430030 [2]三峡大学医学院第一临床学院妇产科
出 处:《中国肿瘤临床》2004年第9期485-488,共4页Chinese Journal of Clinical Oncology
基 金:国家重点基础研究发展项目(编号:2002CB513100);国家杰出青年科学基金项目资助(编号:30025017)
摘 要:目的:探讨针对肺耐药基因(LRPgene)设计的反义寡核苷酸(AsODN)对人卵巢癌多药耐药细胞系OVCAR-3顺铂(DDP)耐药性的逆转作用。方法:采用罗丹明B(SRB)显色法检测LRPAsODN和DDP细胞毒性作用;采用脂质体(lipofectamine2000)介导LRPAsODN转染人卵巢癌多药耐药细胞系OVCAR-3;采用逆转录酶链式反应(RT-PCR)和Westernblot法检测LRPAsODN转染前后OVCAR-3细胞中LRP的表达;采用流式细胞仪测定OVCAR-3细胞在顺铂作用后的凋亡率。结果:LRPAsODN浓度低于800nmol/L时,对OVCAR-3细胞无明显细胞毒作用;LRPAsODN能明显减少OVCAR-3细胞中LRPmRNA和蛋白的表达,增加其顺铂敏感性,且与剂量呈正相关;转染LRPAsODN前后的OVCAR-3细胞在DDP作用后,凋亡率分别为(15.43±1.14)%和(27.43±2.05)%,两者间差异有显著性意义(P=0.001)。结论:LRPAsODN能有效阻断OVCAR-3细胞内LRP的表达,恢复细胞对DDP的敏感性。Objective: To evaluate the effect of antisense oligonucleotide(AsODN), which was targeted at LRP gene, on reverting cisplatin-resistance of multidrug-resistant human ovarian cancer cell line OVCAR-3. Methods: The cytotoxicity of LRP AsODN and cisplatin, or comined both of them were assayed by sulforhodanmine B(SRB) method. LRP AsODN was transfected into OVCAR-3 cell by lipofectamine 2000. The expression of LRP was monitored by RT-PCR and Western blot in LRP AsODN transfected and non-transfected OVCAR-3 cells and the apopototic rates of both cells were detected by flowcytometry after having been treaded with cisplatin. Results: The cytotoxity of LRP AsODN was very low when its concentration was under 800nmol/L. The expression of LRP mRNA and protein were inhibited and a positive drug resistance to cisplatin was observed after LRP AsODN was transfected into OVCAR-3 cells. The apopototic rates of LRP AsODN transfected and non-transfected cells were (27.43±2.05)% and (15.43±1.14)% respectively, the difference was statistically significant(P=0.001). Conclusion: Transfection of LRP AsODN could interrupt the expression of LRP and restore drug sensitivity to cisplatin in multidrug-resistant human ovarian cancer cell line OVCAR-3.
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