Department of Radiology and Imaging Sciences, Emory University, Atlanta, Georgia 30322, USA.
Pharm Res. 2011 Dec;28(12):3091-100. doi: 10.1007/s11095-011-0570-y. Epub 2011 Aug 19.
To explore whether miR-19 is involved in the regulation of multidrug resistance (MDR), one of the main causes of breast cancer mortality, and modulates sensitivity of tumor cells to chemotherapeutic agents.
We analyzed miRNA expression levels in three MDR cell lines in comparison with their parent cell line, MCF-7, using a miRNA microarray. We investigated whether inhibitor of miR-19 sensitized MDR cells to chemotherapeutic agents in vitro and in vivo.
MiR-19 was overexpressed in all three MDR cell lines compared to their parental cell line, MCF-7. Expression levels of miR-19 in MDR cells were inversely consistent with those of PTEN. Inhibitor of miR-19a restored sensitivity of MDR cells to cytotoxic agents; administration of LNA-antimiR-19a, a chemo-modified miR-19a inhibitor, sensitized MDR cells to chemotherapeutic agents in vivo.
Our findings demonstrate, for the first time, involvement of miR-19 in multidrug resistance through modulation of PTEN and suggest that miR-19 may be a potential target for preventing and reversing MDR in tumor cells.
探讨 miR-19 是否参与调节多药耐药(MDR),这是导致乳腺癌死亡的主要原因之一,并调节肿瘤细胞对化疗药物的敏感性。
我们使用 miRNA 微阵列分析了三种 MDR 细胞系与亲本细胞系 MCF-7 之间的 miRNA 表达水平。我们研究了 miR-19 抑制剂是否能在体外和体内增强 MDR 细胞对化疗药物的敏感性。
与亲本细胞系 MCF-7 相比,所有三种 MDR 细胞系中 miR-19 的表达均升高。MDR 细胞中 miR-19 的表达水平与 PTEN 的表达水平呈负相关。miR-19a 抑制剂恢复了 MDR 细胞对细胞毒性药物的敏感性;给予 LNA-antimiR-19a,一种化学修饰的 miR-19a 抑制剂,能在体内增强 MDR 细胞对化疗药物的敏感性。
我们的研究结果首次表明,miR-19 通过调节 PTEN 参与多药耐药,并表明 miR-19 可能是预防和逆转肿瘤细胞多药耐药的潜在靶点。