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作 者:蒋明东[1] 向廷秀[2] 李少林[3] 鄢勇[1] 王正洪[1] 方亮[1] 黄小波[1] 赵瑜[1]
机构地区:[1]重庆市第九人民医院肿瘤科,400700 [2]重庆医科大学附属第一医院实验研究中心 [3]重庆医科大学核医学教研室
出 处:《中华超声影像学杂志》2008年第3期258-261,共4页Chinese Journal of Ultrasonography
基 金:国家自然科学基金资助项目(30070230和30570523)
摘 要:目的探讨超声造影剂联合超声介导mdr1、mrp基因反义寡脱氧核苷酸(ASODN)转染QGY耐药肝癌细胞对多药耐药(MDR)的逆转。方法分别将mdr1、mrp-ASODN+超声造影剂+超声辐照转染QGY/CDDP肝癌细胞,检测转染后细胞贴壁率、药物敏感性、耐药基因mRNA表达和相应耐药蛋白表达变化。结果mdr1—ASODN转染后,细胞贴壁率和耐药基因mRNA表达变化大(P〈0.05),细胞药物敏感性和耐药蛋白P-gp、MRP表达变化小(P〉0.05)。实验组(2组)作用更大(P〈0.05)。mrp—As0DN转染后,细胞贴壁率、药物敏感性、耐药基因的mRNA表达和耐药蛋白P-gp、MRP表达均变化明显(P〈().05),实验组(2组)作用更大(P〈0.05)。结论mdrl、mrp—ASODN+超声造影剂+超声辐照能够低毒部分逆转肝癌细胞MDR,是潜在肿瘤基因治疗方法。Objective To discuss the effect of QGY/CDDP hepatoma lines multi-drug resistance (MDR) reversed by gene transfection of mdrl, mrp-ASODN + ultrasound contrast agent + ultrasound. Methods The QGY/CDDP cells were transfected by mdrl, mrp-ASODN + ultrasound contrast agent + ultrasound irradiation respectively and detected of the various indicators:cell adhesion rate,cell sensitivity to cell drug-resistance, the mRNA expression of mdrl and mrp gene, the expression of P-gp and MRP protein. Results After mdrl-ASODN transfection, the drug sensitivity and expression of P-gp, MRP protein of QGY/CDDP cells were smaller changes( P 〉0.05) ,and the rate of cells adherent and expression of resistance gene mRNA were obvious changes (P 〈 0. 05). After mrp-ASODN transfection, the cells adherent rate, the drug sensitivity, the expression of resistance gene mRNA and P-gp, MRP protein were obvious changes respectively( P 〈0.05 ), the experiment group(group 2') had bigger effects( P 〈0.05 ). Conclusions mdrl, mrp-ASODN + ultrasound contrast agent + ultrasound irradiation could safely partly reverse MDR of hepatoma cells,which is a potential new approach for gene therapy.
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