Hu Haihong, Wang Yu, Qin Zhiyuan, Sun Wen, Chen Yanhong, Wang Jiaqi, Wang Yingying, Nie Jing, Chen Lu, Cai Sheng, Yu Lushan, Zeng Su
Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, Cancer Center of Zhejiang University, Hangzhou 310058, China.
Institute of Drug Metabolism and Pharmaceutical Analysis, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Biomedicines. 2021 Apr 30;9(5):497. doi: 10.3390/biomedicines9050497.
Multidrug resistance-associated protein 4 (MRP4), a member of the adenosine triphosphate (ATP) binding cassette transporter family, pumps various molecules out of the cell and is involved in cell communication and drug distribution. Several studies have reported the role of miRNAs in downregulating the expression of MRP4. However, regulation of MRP4 by circular RNA (circRNA) is yet to be elucidated. In this study, MRP4 was significantly upregulated in hepatocellular carcinoma (HCC) tissues compared to the adjacent noncancerous tissues. Computational prediction, luciferase reporter assay and miRNA transfection were used to investigate the interaction between miRNAs and MRP4. miR-124-3p and miR-4524-5p reduced the expression of MRP4 at the protein but not mRNA level. Circular RNA in vivo precipitation and luciferase reporter assays demonstrated that circHIPK3, as a competitive endogenous RNA, binds with miR-124-3p and miR-4524-5p. Further, knockdown of circHIPK3 resulted in downregulation of MRP4 protein, whereas cotransfection of circHIPK3-siRNA and miR-124-3p or miR-4524-5p inhibitors restored its expression. In conclusion, we report that miR-4524-5p downregulates the expression of MRP4 and circHIPK3 regulates MRP4 expression by sponging miR-124-3p and miR-4524-5p for the first time. Our results may provide novel insights into the prevention of MRP4-related proliferation and multiple drug resistance in HCC.
多药耐药相关蛋白4(MRP4)是三磷酸腺苷(ATP)结合盒转运体家族的成员之一,可将多种分子泵出细胞,并参与细胞通讯和药物分布。多项研究报道了微小RNA(miRNA)在下调MRP4表达中的作用。然而,环状RNA(circRNA)对MRP4的调控作用尚待阐明。在本研究中,与癌旁非肿瘤组织相比,MRP4在肝细胞癌(HCC)组织中显著上调。采用计算预测、荧光素酶报告基因检测和miRNA转染等方法研究miRNA与MRP4之间的相互作用。miR-124-3p和miR-4524-5p在蛋白质水平而非mRNA水平降低了MRP4的表达。体内环状RNA沉淀和荧光素酶报告基因检测表明,circHIPK3作为一种竞争性内源RNA,可与miR-124-3p和miR-4524-5p结合。此外,敲低circHIPK3导致MRP4蛋白表达下调,而共转染circHIPK3-siRNA与miR-124-3p或miR-4524-5p抑制剂可恢复其表达。总之,我们首次报道miR-4524-5p下调MRP4的表达,且circHIPK3通过海绵吸附miR-