Sun Y-L, Zhou G-Y, Li K-N, Gao P, Zhang Q-H, Zhen J-H, Bai Y-H, Zhang X-F
Department of Pathology, School of Medicine, Shandong University, 250012 Jinan, China.
Neoplasma. 2006;53(1):1-8.
Glucosylceramide synthase (GCS), the enzyme that converts ceramide to glucosylceramide, induce multidrug resistance (MDR) in cancer cells. Recently, RNA interference (RNAi) is a powerful strategy for gene therapy by introducing double-stranded RNA and leading to the sequence-specific destruction. We have designed two different short hairpin RNAs (shRNAs) targeting GCS and introduced them into adriamycin- resistant human breast cancer cells (MCF-7/AdrR cells) to inhibit GCS expression. The results demonstrated that the shRNAs targeting GCS decreased GCS mRNA, abolished GCS protein levels and restored the sensitivity of MCF-7/AdrR cells to several antineoplastic drugs. This study revealed that this approach can reverse MDR effectively and it may be applicable to cancer patients as a specific means to restore the sensitivity to chemotherapy.
葡糖神经酰胺合酶(GCS)是一种将神经酰胺转化为葡糖神经酰胺的酶,可诱导癌细胞产生多药耐药性(MDR)。最近,RNA干扰(RNAi)是一种通过引入双链RNA并导致序列特异性破坏来进行基因治疗的强大策略。我们设计了两种针对GCS的不同短发夹RNA(shRNA),并将它们导入阿霉素耐药的人乳腺癌细胞(MCF-7/AdrR细胞)中以抑制GCS表达。结果表明,靶向GCS的shRNA降低了GCS mRNA水平,消除了GCS蛋白水平,并恢复了MCF-7/AdrR细胞对几种抗肿瘤药物的敏感性。这项研究表明,这种方法可以有效地逆转多药耐药性,并且作为恢复化疗敏感性的一种特定手段,它可能适用于癌症患者。