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LncRNA H19 induced by helicobacter pylori infection promotes gastric cancer cell growth via enhancing NF-κB-induced inflammation.幽门螺杆菌感染诱导的长链非编码RNA H19通过增强核因子κB诱导的炎症促进胃癌细胞生长。
J Inflamm (Lond). 2019 Nov 26;16:23. doi: 10.1186/s12950-019-0226-y. eCollection 2019.
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The Role of Exosomal MicroRNAs in the Tumor Microenvironment of Breast Cancer.外泌体 microRNAs 在乳腺癌肿瘤微环境中的作用。
Int J Mol Sci. 2019 Aug 9;20(16):3884. doi: 10.3390/ijms20163884.
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MicroRNAs: Key Players in Bladder Cancer.微小 RNA:膀胱癌的关键参与者。
Mol Diagn Ther. 2019 Oct;23(5):579-601. doi: 10.1007/s40291-019-00410-4.
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Circulating microRNAs as potential diagnostic biomarkers and therapeutic targets in prostate cancer: Current status and future perspectives.循环 microRNAs 作为前列腺癌潜在的诊断生物标志物和治疗靶点:现状与展望。
J Cell Biochem. 2019 Oct;120(10):16316-16329. doi: 10.1002/jcb.29053. Epub 2019 Jun 30.
5
Exosomal hsa-miR199a-3p Promotes Proliferation and Migration in Neuroblastoma.外泌体人源微小核糖核酸199a-3p促进神经母细胞瘤的增殖和迁移。
Front Oncol. 2019 Jun 12;9:459. doi: 10.3389/fonc.2019.00459. eCollection 2019.
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Hope and challenge: Precision medicine in bladder cancer.希望与挑战:膀胱癌的精准医学。
Cancer Med. 2019 Apr;8(4):1806-1816. doi: 10.1002/cam4.1979. Epub 2019 Mar 24.
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UBIAD1 suppresses the proliferation of bladder carcinoma cells by regulating H-Ras intracellular trafficking via interaction with the C-terminal domain of H-Ras.UBIAD1 通过与 H-Ras 的 C 末端结构域相互作用调节 H-Ras 细胞内转运从而抑制膀胱癌细胞的增殖。
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MicroRNA‑154 functions as a tumor suppressor in bladder cancer by directly targeting ATG7.MicroRNA-154 在膀胱癌中作为肿瘤抑制因子发挥作用,其直接靶向 ATG7。
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A urinary microRNA (miR) signature for diagnosis of bladder cancer.用于诊断膀胱癌的尿液微小RNA(miR)特征
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Exosomes as a liquid biopsy for lung cancer.外泌体作为肺癌的液体活检。
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MiR-4644在膀胱癌患者血浆外泌体中上调,并通过靶向UBIAD1促进膀胱癌进展。

MiR-4644 is upregulated in plasma exosomes of bladder cancer patients and promotes bladder cancer progression by targeting UBIAD1.

作者信息

Yan Liang, Li Qi, Sun Ke, Jiang Fan

机构信息

Department of Urology, The First Affiliated Hospital of Zhengzhou University Zhengzhou 450000, China.

出版信息

Am J Transl Res. 2020 Oct 15;12(10):6277-6289. eCollection 2020.

PMID:33194029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7653622/
Abstract

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.

摘要

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。