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MiR-127 and miR-376a act as tumor suppressors by in vivo targeting of COA1 and PDIA6 in giant cell tumor of bone.miR-127 和 miR-376a 通过体内靶向作用于 COA1 和 PDIA6 抑制骨巨细胞瘤的生长。
Cancer Lett. 2017 Nov 28;409:49-55. doi: 10.1016/j.canlet.2017.08.029. Epub 2017 Sep 1.
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Long Noncoding RNA H19/miR-675 Axis Promotes Gastric Cancer via FADD/Caspase 8/Caspase 3 Signaling Pathway.长链非编码RNA H19/miR-675轴通过FADD/半胱天冬酶8/半胱天冬酶3信号通路促进胃癌发生。
Cell Physiol Biochem. 2017;42(6):2364-2376. doi: 10.1159/000480028. Epub 2017 Aug 18.
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A microRNA-7/growth arrest specific 6/TYRO3 axis regulates the growth and invasiveness of sorafenib-resistant cells in human hepatocellular carcinoma.一个 microRNA-7/生长停滞特异性 6/TYRO3 轴调节人肝癌索拉非尼耐药细胞的生长和侵袭。
Hepatology. 2018 Jan;67(1):216-231. doi: 10.1002/hep.29478. Epub 2017 Nov 29.
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MicroRNA-218 functions as a tumor suppressor in lung cancer by targeting IL-6/STAT3 and negatively correlates with poor prognosis.MicroRNA-218 通过靶向 IL-6/STAT3 发挥抑癌作用,与不良预后呈负相关。
Mol Cancer. 2017 Aug 22;16(1):141. doi: 10.1186/s12943-017-0710-z.
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miR-10b is a prognostic marker in clear cell renal cell carcinoma.微小RNA-10b是透明细胞肾细胞癌的一种预后标志物。
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MicroRNAs in clear cell renal cell carcinoma: biological functions and applications.透明细胞肾细胞癌中的微小RNA:生物学功能与应用
J Kidney Cancer VHL. 2015 Aug 23;2(4):140-152. doi: 10.15586/jkcvhl.2015.40. eCollection 2015.
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Renal cell carcinoma.肾细胞癌。
Nat Rev Dis Primers. 2017 Mar 9;3:17009. doi: 10.1038/nrdp.2017.9.
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Therapeutic Potentials of BDNF/TrkB in Breast Cancer; Current Status and Perspectives.BDNF/TrkB在乳腺癌中的治疗潜力:现状与展望
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MicroRNA-191 acts as a tumor promoter by modulating the TET1-p53 pathway in intrahepatic cholangiocarcinoma.MicroRNA-191 通过调节 TET1-p53 通路在肝内胆管癌中发挥肿瘤促进作用。
Hepatology. 2017 Jul;66(1):136-151. doi: 10.1002/hep.29116. Epub 2017 May 18.
10
Anti-GD2-ch14.18/CHO coated nanoparticles mediate glioblastoma (GBM)-specific delivery of the aromatase inhibitor, Letrozole, reducing proliferation, migration and chemoresistance in patient-derived GBM tumor cells.抗GD2-ch14.18/CHO包被的纳米颗粒介导芳香化酶抑制剂来曲唑对胶质母细胞瘤(GBM)的特异性递送,降低患者来源的GBM肿瘤细胞的增殖、迁移和化疗耐药性。
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微小RNA-191-5p在肾细胞癌中发挥肿瘤抑制作用。

MicroRNA-191-5p exerts a tumor suppressive role in renal cell carcinoma.

作者信息

Chen Peijie, Pan Xiang, Zhao Liwen, Jin Lu, Lin Canbin, Quan Jing, He Tao, Zhou Liang, Wu Xueling, Wang Yong, Ni Liangchao, Yang Shangqi, Lai Yongqing

机构信息

Department of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.

Department of Urology, Shantou University Medical College, Shantou, Guangdong 515041, P.R. China.

出版信息

Exp Ther Med. 2018 Feb;15(2):1686-1693. doi: 10.3892/etm.2017.5581. Epub 2017 Nov 28.

DOI:10.3892/etm.2017.5581
PMID:29434754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5774385/
Abstract

Renal cell carcinoma (RCC) is a common tumor of the urinary system. Previously, miR-191-5p has been reported to be associated with various types of cancer; however, its specific functions in RCC have not been investigated to date. In the present study, the expression of miR-191-5p in the 786-O and ACHN cell lines was detected by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The results of RT-qPCR revealed that miR-191-5p was significantly downregulated in the two cell lines compared with the 293T cell line. miR-191-5p was also significantly downregulated in RCC tissue compared with paired normal tissue. In addition, the effects of miR-191-5p on cell proliferation, migration, invasion and apoptosis were examined by CCK-8, MTT, wound scratch, Transwell and flow cytometry assays. Downregulation of miR-191-5p was observed to promote cell proliferation, migration and invasion, as well as to repress the cell apoptosis of 786-O and ACHN cells. Therefore, the current study suggests that miR-191-5p functions as a tumor suppressor in RCC. Further studies are required to uncover the underlying signaling pathway of miR-191-5p and its potential role as a biomarker for early detection and prognosis prediction, and as a therapeutic target of RCC.

摘要

肾细胞癌(RCC)是泌尿系统的常见肿瘤。此前,已有报道称miR-191-5p与多种类型的癌症相关;然而,其在RCC中的具体功能迄今尚未得到研究。在本研究中,通过逆转录-定量聚合酶链反应(RT-qPCR)检测了miR-191-5p在786-O和ACHN细胞系中的表达。RT-qPCR结果显示,与293T细胞系相比,miR-191-5p在这两种细胞系中显著下调。与配对的正常组织相比,miR-191-5p在RCC组织中也显著下调。此外,通过CCK-8、MTT、划痕试验、Transwell和流式细胞术检测了miR-191-5p对细胞增殖、迁移、侵袭和凋亡的影响。观察到miR-191-5p的下调促进了786-O和ACHN细胞的增殖、迁移和侵袭,并抑制了细胞凋亡。因此,当前研究表明miR-191-5p在RCC中发挥肿瘤抑制作用。需要进一步研究以揭示miR-191-5p的潜在信号通路及其作为早期检测和预后预测生物标志物以及RCC治疗靶点的潜在作用。