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本文引用的文献

1
Targeting non-coding RNA for the therapy of renal disease.靶向非编码RNA治疗肾脏疾病
Curr Opin Pharmacol. 2016 Apr;27:70-7. doi: 10.1016/j.coph.2016.02.001. Epub 2016 Feb 26.
2
Expression and functional role of miR-29b in renal cell carcinoma.miR-29b在肾细胞癌中的表达及功能作用
Int J Clin Exp Pathol. 2015 Nov 1;8(11):14161-70. eCollection 2015.
3
Downregulation of miR-30c promotes renal fibrosis by target CTGF in diabetic nephropathy.在糖尿病肾病中,miR-30c的下调通过靶向结缔组织生长因子(CTGF)促进肾纤维化。
J Diabetes Complications. 2016 Apr;30(3):406-14. doi: 10.1016/j.jdiacomp.2015.12.011. Epub 2015 Dec 17.
4
Downregulation of microRNA-206 suppresses clear cell renal carcinoma proliferation and invasion by targeting vascular endothelial growth factor A.微小RNA-206的下调通过靶向血管内皮生长因子A抑制肾透明细胞癌的增殖和侵袭。
Oncol Rep. 2016 Mar;35(3):1778-86. doi: 10.3892/or.2015.4538. Epub 2015 Dec 30.
5
MicroRNA21 promotes interstitial fibrosis via targeting DDAH1: a potential role in renal fibrosis.微小RNA21通过靶向二甲基精氨酸二甲胺水解酶1促进间质纤维化:在肾纤维化中的潜在作用
Mol Cell Biochem. 2016 Jan;411(1-2):181-9. doi: 10.1007/s11010-015-2580-2. Epub 2015 Oct 12.
6
miR-372 suppresses tumour proliferation and invasion by targeting IGF2BP1 in renal cell carcinoma.微小RNA-372通过靶向胰岛素样生长因子2结合蛋白1抑制肾细胞癌的肿瘤增殖和侵袭。
Cell Prolif. 2015 Oct;48(5):593-9. doi: 10.1111/cpr.12207.
7
Tumour-suppressive microRNA-29s directly regulate LOXL2 expression and inhibit cancer cell migration and invasion in renal cell carcinoma.抑瘤 microRNA-29s 可直接调控 LOXL2 的表达,从而抑制肾细胞癌中癌细胞的迁移和侵袭。
FEBS Lett. 2015 Jul 22;589(16):2136-45. doi: 10.1016/j.febslet.2015.06.005. Epub 2015 Jun 19.
8
miR-514a regulates the tumour suppressor NF1 and modulates BRAFi sensitivity in melanoma.微小RNA-514a调控肿瘤抑制因子神经纤维瘤病1型,并调节黑色素瘤对BRAF抑制剂的敏感性。
Oncotarget. 2015 Jul 10;6(19):17753-63. doi: 10.18632/oncotarget.3924.
9
Prognostic value of meta-signature miRNAs in renal cell carcinoma: an integrated miRNA expression profiling analysis.元特征性微小RNA在肾细胞癌中的预后价值:一项整合的微小RNA表达谱分析
Sci Rep. 2015 May 14;5:10272. doi: 10.1038/srep10272.
10
MicroRNA-509-3p inhibits cancer cell proliferation and migration by targeting the mitogen-activated protein kinase kinase kinase 8 oncogene in renal cell carcinoma.微小RNA-509-3p通过靶向肾细胞癌中的丝裂原活化蛋白激酶激酶激酶8癌基因来抑制癌细胞的增殖和迁移。
Mol Med Rep. 2015 Jul;12(1):1535-43. doi: 10.3892/mmr.2015.3498. Epub 2015 Mar 17.

miR-514a-3p在肾细胞癌中发挥肿瘤抑制作用。

miR-514a-3p functions as a tumor suppressor in renal cell carcinoma.

作者信息

Jin Lu, Li Yifan, Zhang Zeng, He Tao, Hu Jia, Liu Jiaju, Chen Mingwei, Gui Yaoting, Yang Shangqi, Mao Xiangming, Chen Yun, Lai Yongqing

机构信息

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

Department of Urology, Anhui Medical University, Hefei, Anhui 230032, P.R. China.

出版信息

Oncol Lett. 2017 Nov;14(5):5624-5630. doi: 10.3892/ol.2017.6855. Epub 2017 Aug 31.

DOI:10.3892/ol.2017.6855
PMID:29113192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5661369/
Abstract

Renal cell carcinoma (RCC) is the most common type of kidney cancer, and the prognosis of metastatic RCC remains poor with a high rate of recurrence and mortality. A previous study has revealed that microRNA (miRNA), which negatively regulates protein expression, serves a role of oncogene or tumor suppressor. The aim of the present study was to investigate the expression and function of miR-514a-3p in RCC. To detect the expression of miR-514a-3p in 32 paired RCC tissues, quantitative polymerase chain reaction (qPCR) was performed. The function of miR-514a-3p in the proliferation, mobility and apoptosis of RCC cells (786-O and ACHN) was assessed by MTT, CCK-8, cell scratch, Transwell, Hoechst 33342 staining and flow cytometry assay. The results of qPCR revealed that miR-514a-3p was significantly downregulated in RCC tissues compared with adjacent normal tissues. Upregulation of miR-514a-3p by transfection of mimics suppressed RCC cell proliferation, migration and invasion, and induced cell apoptosis. The results revealed that miR-514a-3p was significantly downregulated in RCC and may serve a role as tumor suppressor in RCC. Further studies are required, focusing on the possibility of using miR-514a-3p as a biomarker for RCC as well as the pathway of miR-514a-3p in RCC.

摘要

肾细胞癌(RCC)是最常见的肾癌类型,转移性RCC的预后仍然很差,复发率和死亡率很高。先前的一项研究表明,负向调节蛋白质表达的微小RNA(miRNA)发挥癌基因或肿瘤抑制因子的作用。本研究的目的是调查miR-514a-3p在RCC中的表达和功能。为检测32对RCC组织中miR-514a-3p的表达,进行了定量聚合酶链反应(qPCR)。通过MTT、CCK-8、细胞划痕、Transwell、Hoechst 33342染色和流式细胞术检测评估miR-514a-3p在RCC细胞(786-O和ACHN)增殖、迁移和凋亡中的作用。qPCR结果显示,与相邻正常组织相比,RCC组织中miR-514a-3p明显下调。通过转染模拟物上调miR-514a-3p可抑制RCC细胞增殖、迁移和侵袭,并诱导细胞凋亡。结果表明,miR-514a-3p在RCC中明显下调,可能在RCC中发挥肿瘤抑制因子的作用。需要进一步研究,重点关注将miR-514a-3p用作RCC生物标志物的可能性以及miR-514a-3p在RCC中的作用途径。