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mdr1反义寡核苷酸增强多药耐药肝癌细胞HepG2/ADM化疗敏感性的实验研究

Experimental research of chemotherapeutic sensitization for multidrug resistance hepatocellular carcinoma cell HepG2/ADM enhanced by mdr1antisense oligonucleotides

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【作者】 廖奎刘双何燕琼蒋明东李少林彭志平

【Author】 Liao Kui;Liu Shuang;He Yanqiong;Jiang Mingdong;Li Shaolin;Peng Zhiping;Department of Oncology,the First Affiliated Hospital of Chongqing Medical University;Department of Radiological Medicine,Chongqing Medical University;

【机构】 重庆医科大学附属第一医院肿瘤科重庆医科大学基础医学院放射医学教研室

【摘要】 目的探讨在体外实验条件下mdr1反义寡核苷酸对多药耐药肝癌细胞株化疗敏感性的影响。方法以肝癌细胞Hep G2/ADM为研究对象,设立mdr1反义寡核苷酸组和空白试剂组作对照,利用脂质体包载肿瘤耐药基因mdr1的反义寡核苷酸进行细胞转染,通过反转录聚合酶链反应(RT-PCR)、免疫印迹实验(Western blotting)分别检测mdr1基因m RNA和P-gp蛋白表达,通过MTT实验检测细胞转染前后对阿霉素(ADM)、顺铂(DDP)和5-氟尿嘧啶(5-FU)的化疗敏感性。结果 Hep G2/AMD肝癌细胞经反义寡核苷酸处理后,mdr1m RNA、P-gp蛋白表达水平均明显降低,对ADM、DDP和5-FU的化疗敏感性明显增强。结论反义寡核苷酸能在体外有效增加肝癌细胞Hep G2/ADM对化疗药物的敏感性。

【Abstract】 Objective To study the effect of mdr1 genes antisense oligonucleotides in vitro on chemotherapeutic sensitization for multidrug resistance hepatocellular carcinoma cell lines. Methods The hepatocellular carcinoma cell Hep G2/ADM was taken as research object,and mdr1 genes antisense oligonucleotides group and blank control group were established. The cell transfection was conducted by antisense oligonucleotides of liposome entrapment drug resistance gene mdr1. The protein expressions of m RNA and P-gp of mdr1 gene were detected by reverse transcription-polymerase chain reaction(RT-PCR) and Western blotting respectively,while the chemotherapeutic sensitization to ADM,DDP and 5-FU before and after cell transfection by MTT.Results After transfecting by antisense oligonucleotides,the protein expression levels of mdr1,m RNA and P-gp in hepatocellular carcinoma cell Hep G2/ADM decreased obviously,and the chemotherapeutic sensitization to ADM,DDP and 5-FU increased prominently. Conclusion The antisense oligonucleotides can improve the sensitization of Hep G2/ADM to chemotherapy drugs in vitro.

【基金】 国家自然科学基金(81171365);重庆市自然科学基金(2010BB5358)
  • 【文献出处】 现代医药卫生 ,Journal of Modern Medicine & Health , 编辑部邮箱 ,2014年22期
  • 【分类号】R735.7
  • 【被引频次】1
  • 【下载频次】76
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