Yan Liang, Li Qi, Sun Ke, Jiang Fan
Department of Urology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450000, China.
Am J Transl Res. 2020 Oct 15;12(10):6277-6289. eCollection 2020.
Exosome-encapsulated microRNAs (miRNAs) have been identified as potential cancer biomarkers and pro-tumorigenic mediators for several cancers. However, the miRNA profiling in BCa-Exo (exosomes from plasma of patients with bladder cancer) has not yet been explored. Hence, the aim of this study was to analyze the miRNA profiling in BCa-Exo and to explore the function and mechanism of the selected miR-4644 in BCa progression. Of the 8 differentially expressed miRNAs in BCa-Exo relative to NC-Exo (exosomes from plasma of normal control subjects), hsa-miR-4644 was the only upregulated (fold change >2.0, <0.05) miRNA, which was further confirmed to be upregulated in plasma of BCa patients and BCa cell lines. Further assays demonstrated that miR-4644 mimic promoted, whereas miR-4644 inhibitor suppressed BCa cell proliferation and invasion. miR-4644 negatively regulated expression of UBIAD1 (UbiA prenyltransferase domain-containing protein 1) by directly binding to its 3'-UTR region. UBIAD1 overexpression effectively abrogated the promoting effects of miR-4644 mimic on BCa proliferation, migration, and invasion. Additionally, intratumoral injection of miR-4644 antagomir downregulated miR-4644 expression in tumors and suppressed tumorigenesis in mouse xenografts. Collectively, miR-4644 promotes BCa progression by targeting UBIAD1. miR-4644 may be an important therapeutic target for BCa treatment.
外泌体包裹的微小RNA(miRNA)已被确定为几种癌症的潜在生物标志物和促肿瘤发生介质。然而,膀胱癌外泌体(BCa-Exo,来自膀胱癌患者血浆的外泌体)中的miRNA谱尚未得到研究。因此,本研究的目的是分析BCa-Exo中的miRNA谱,并探讨所选miR-4644在膀胱癌进展中的功能和机制。在与正常对照受试者血浆来源的外泌体(NC-Exo)相比,BCa-Exo中8种差异表达的miRNA中,hsa-miR-4644是唯一上调(倍数变化>2.0,<0.05)的miRNA,进一步证实在膀胱癌患者血浆和膀胱癌细胞系中其表达上调。进一步的实验表明,miR-4644模拟物促进,而miR-4644抑制剂抑制膀胱癌细胞的增殖和侵袭。miR-4644通过直接结合其3'-UTR区域负调控含泛醌A异戊二烯基转移酶结构域蛋白1(UBIAD1)的表达。UBIAD1过表达有效消除了miR-4644模拟物对膀胱癌增殖、迁移和侵袭的促进作用。此外,瘤内注射miR-4644拮抗剂可下调肿瘤中miR-4644的表达,并抑制小鼠异种移植瘤的发生。总体而言,miR-4644通过靶向UBIAD1促进膀胱癌进展。miR-4644可能是膀胱癌治疗的重要治疗靶点。