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作 者:李璐璐[1] 迟寿军[2] 王莹[1] 井欢[3] 刘春英[1]
机构地区:[1]辽宁中医药大学基础医学院病理教研室,沈阳110032 [2]辽宁中医药大学基础医学院中医基础教研室,沈阳110032 [3]辽宁中医药大学重大科研平台显微形态实验中心,沈阳110032
出 处:《重庆医科大学学报》2014年第9期1211-1214,共4页Journal of Chongqing Medical University
基 金:国家自然科学基金资助项目(编号:81072743);辽宁省自然基金资助项目(编号:20102145)
摘 要:目的:运用小干扰RNA片段(small interfering RNA,siRNA)的方法特异性沉默肺耐药蛋白(lung resistance protein,LRP)基因,观测该方法同补中益气汤含药血清联合应用逆转人肺腺癌耐药细胞A549/DDP的效果。方法:设计并合成针对LRP基因对应序列的siRNA,采用转染试剂对细胞进行转染。实验分组为:空白对照组、补中益气汤含药血清组、siRNA组及补中益气汤含药血清+siRNA组,利用逆转录聚合酶链反应(reverse transcription-polymerase chain reaction,RT-PCR)检测对该基因的抑制作用,Western blot及免疫细胞化学法检测蛋白质表达。结果:参照空白对照组,补中益气汤含药血清组、siRNA组及补中益气汤含药血清+siRNA组mRNA及LRP蛋白表达均减少,差异有统计学意义(P<0.05)。结论:补中益气汤含药血清和siRNA均能降低A549/DDP的LRP蛋白表达,并且2种因素之间存在交互作用。Objective:To discuss the effect of concomitant application of small interfering RNA(siRNA)after targeted resection of lung resistance protein(LRP)and Buzhongyiqitang serum on the human lung adenocarcinoma drug-resistant cell-line A549/DDP. Methods:The siRNAs which had the same sequences of LRP gene were designed and synthesized,then the human lung adenocarcinoma drug-resistant cell-line A549/DPP was transected with transfection reagent. The experimental cells were grouped into control group,Buzhongyiqitang serum group,siRNA-processed group and Buzhongyiqitang plus siRNA-processed group. RT-PCR was applied to determine the mRNA expression of LRP. Western blot and immunocytochemical method were adopted to determine the protein expression of LRP. Results:Protein and mRNA expression of LRP in Buzhongxiqitang serum group,siRNA group and Buzhongyiqitang plus siRNA-processed group was decreased significantly compared with that in control group(P〈0.05). Conclusion:Both Buzhongyiqitang serum and siRNA serve effectively in decreasing protein expression of LRP,and Buzhongyiqitang serum combined siRNA show synergistic effect.
关 键 词:补中益气汤 小干扰RNA片段 A549/DDP细胞 肺耐药蛋白
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