Department of Biochemistry and Molecular Biology, Central University of Kerala Periye, Kerala 671316, India.
Department of Medicine, Thomas Jefferson University, Jefferson Alumni Hall, 1020 Locust Street, Philadelphia, PA 19107, USA.
Cells. 2021 May 28;10(6):1341. doi: 10.3390/cells10061341.
Acquisition of resistance to cisplatin is a major impediment to the success of cisplatin-based combination therapies for cancer. Recent studies indicate that exosomal miRNAs derived from drug-resistant tumour cells can confer resistance properties to recipient cells by a horizontal transfer mechanism. Although the role of horizontal transfer of a few miRNAs has been described, little is known about the concerted action of horizontal transfer of miRNAs in conferring cisplatin resistance. The present study was designed to identify the role of miR-643, which is one of the most significantly increased miRNA in exosomes released from cisplatin-resistant Heptocarcinoma cells, in altering the cisplatin resistance properties of recipient cells. Drug-sensitivity assays involving miR-643 revealed that ectopic expression of miR-643 can desensitise the cells towards cisplatin. Furthermore, we identified APOL6 as a major target of miR-643. Further mechanistic studies showed that miR-643 can modulate APOL6 mRNA and protein levels, leading to a reversal of APOL6-mediated apoptosis. Altogether, our results suggest an APOL6-dependent mechanism for miR-643 mediated cisplatin resistance upon the horizontal transfer across cell types.
获得对顺铂的耐药性是顺铂为基础的联合疗法治疗癌症成功的主要障碍。最近的研究表明,来源于耐药肿瘤细胞的外泌体 miRNA 可以通过水平转移机制将耐药特性赋予受体细胞。虽然已经描述了少数 miRNA 的水平转移作用,但对于 miRNA 水平转移在赋予顺铂耐药性中的协同作用知之甚少。本研究旨在确定 miR-643 的作用,miR-643 是从顺铂耐药肝癌细胞释放的外泌体中增加最显著的 miRNA 之一,在改变受体细胞的顺铂耐药性方面。涉及 miR-643 的药物敏感性测定表明,miR-643 的异位表达可以使细胞对顺铂脱敏。此外,我们鉴定出 APOL6 是 miR-643 的主要靶标。进一步的机制研究表明,miR-643 可以调节 APOL6 mRNA 和蛋白水平,导致 APOL6 介导的细胞凋亡逆转。总之,我们的研究结果表明,miR-643 通过细胞间的水平转移介导顺铂耐药性的机制依赖于 APOL6。