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作 者:魏军民[1] 侯明[1] 李丽珍[1] 孔峰[2] 高鹏[3]
机构地区:[1]山东大学齐鲁医院肿瘤中心,济南250012 [2]山东大学医学院分子生物学教研室 [3]山东大学医学院病理教研室
出 处:《中华乳腺病杂志(电子版)》2008年第4期29-32,共4页Chinese Journal of Breast Disease(Electronic Edition)
摘 要:目的探讨针对多药耐药基因(MDR-1)的小分子干扰RNA(siRNAs)和反义脱氧寡核苷酸(asODNs)联合应用逆转人乳腺癌细胞MCF-7/ADR的作用效果。方法设计并合成针对MDR-1基因同一序列的siRNAs和asODNs及阴性对照siRNAs,采用转染试剂lipofectamineTM2000分别转染人乳腺癌耐药细胞MCF-7/ADR;利用RT-PCR检测MDR-1mRNA和Western blot检测MDR-1蛋白质的表达;采用罗丹明123外排实验检测P-gp的转运功能,MTT法检测MCF-7/ADR细胞对阿霉素的耐药逆转效果。结果siRNAs、asODNs、asODNs和siRNAs联合应用均能降低MDR-1mRNA及其蛋白质表达,提高P-gp的转运功能,使细胞对阿霉素的敏感性明显恢复;asODNs和siRNAs联合应用效果明显提高;低浓度siRNAs(200nmol/L)比高浓度asODNs(5μmol/L)的效果强。结论siRNAs、asODNs能有效逆转人乳腺癌细胞MCF-7/ADR的多药耐药,asODNs和siRNAs联合应用效果明显加强。Objective To study the effect of small interfering RNAs(siRNAs) combined with antisense oligodeoxyribonucleotides (asODNs) , which targeted MDR1 gene, on reversing multidrug resistance of human breast cancer cell line MCF-7/ADR. Methods The siRNAs and asODNs which targeted the same sequences of MDR1 gene were designed and synthesized. Human breast cancer MCF-7/ADR cells were cultured and tranfected with asODNs, siRNAs + asODNs, siRNAs, and negative siRNAs using lipofectamineTM 2000, respectively. MDR-1mRNA was assayed by RT-PCR and the protein expression was detected by Western blotting. The function of P-glycoprotein (P-gp) was detected by rhodamine 123 retention and the resistant efficiency of MCF-7/ADR to ADM was determined by MTT method. Results The expressions of MDR-lmRNA and protein decreased significantly after transfection of asODNs, siRNAs + asODNs, and siRNAs respectively. The transporting function of P-gp increased and the resistance of MCF-7/ADR to ADM reversed significantly. The reversing effect increased significantly by siRNAs combined with asODNs. The inhibition effect of the siRNAs with lower concentration (200 nmol/L)was greater than that of asODNs with higher concentration (5 umol/L). Conclusion siRNAs and asODNs could reverse multidmg resistance of human breast cancer cell line MCF-7/ADR. The inhibition effect is increased significantly by siRNAs combined with asODNs.
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