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Am J Transl Res. 2019 May 15;11(5):3081-3091. eCollection 2019.
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MiR-27a-regulated FOXO1 promotes pancreatic ductal adenocarcinoma cell progression by enhancing Wnt/β-catenin signaling activity.MiR-27a调控的FOXO1通过增强Wnt/β-连环蛋白信号活性促进胰腺导管腺癌细胞进展。
Am J Transl Res. 2019 May 15;11(5):3069-3080. eCollection 2019.
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MiR-30a regulates cancer cell response to chemotherapy through SNAI1/IRS1/AKT pathway.miR-30a 通过 SNAI1/IRS1/AKT 通路调节癌细胞对化疗的反应。
Cell Death Dis. 2019 Feb 15;10(3):153. doi: 10.1038/s41419-019-1326-6.
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MicroRNA-30a suppresses the proliferation, migration and invasion of human renal cell carcinoma cells by directly targeting ADAM9.微小RNA-30a通过直接靶向解聚素金属蛋白酶9抑制人肾癌细胞的增殖、迁移和侵袭。
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5
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J Physiol Pharmacol. 2018 Apr;69(2). doi: 10.26402/jpp.2018.2.07. Epub 2018 Jul 4.
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World J Gastroenterol. 2017 Dec 7;23(45):7965-7977. doi: 10.3748/wjg.v23.i45.7965.
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A novel culture system robustly maintained pluripotency of embryonic stem cells and accelerated somatic reprogramming by activating Wnt signaling.一种新型培养系统通过激活Wnt信号通路,有力地维持了胚胎干细胞的多能性并加速了体细胞重编程。
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MiR-665 regulates VSMCs proliferation via targeting FGF9 and MEF2D and modulating activities of Wnt/β-catenin signaling.微小RNA-665通过靶向成纤维细胞生长因子9和肌细胞增强因子2D并调节Wnt/β-连环蛋白信号通路的活性来调控血管平滑肌细胞的增殖。
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miR-30a acts as a tumor suppressor by double-targeting COX-2 and BCL9 in H. pylori gastric cancer models.miR-30a 通过双重靶向 COX-2 和 BCL9 在 H. pylori 胃癌模型中发挥肿瘤抑制作用。
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Downregulation of miR-193a-3p inhibits cell growth and migration in renal cell carcinoma by targeting PTEN.miR-193a-3p的下调通过靶向PTEN抑制肾细胞癌的细胞生长和迁移。
Tumour Biol. 2017 Jun;39(6):1010428317711951. doi: 10.1177/1010428317711951.

微小RNA-30a-3p通过靶向WNT2在肾细胞癌中发挥肿瘤抑制作用。

MicroRNA-30a-3p functions as a tumor suppressor in renal cell carcinoma by targeting WNT2.

作者信息

Liu Lingqi, Chen Liang, Wu Tianpeng, Qian Huijun, Yang Sixing

机构信息

Department of Urology, Renmin Hospital of Wuhan University Wuhan 430060, Hubei, China.

出版信息

Am J Transl Res. 2019 Aug 15;11(8):4976-4983. eCollection 2019.

PMID:31497214
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6731429/
Abstract

The expression and function of microRNA (miR)-30a-3p in several types of human cancer have been explored. However, the biological function of miR-30a-3p in renal cell carcinoma (RCC) remains largely unknown. In this study, we demonstrate that expression of miR-30a-3p is down-regulated in RCC tissues compared to adjacent normal tissues. Furthermore, ectopic expression of miR-30a-3p significantly suppressed the proliferation, migration, and invasion of a human RCC cell line , while miR-30a-3p inhibited tumor growth as well. TargetScan software identified Wnt2 as a potential direct target of miR-30a-3p. To confirm this relationship, Wnt2 was ectopically expressed. The effects of miR-30a-3p on RCC cell proliferation and invasion were subsequently restored. Therefore, the results of this study support an anti-tumor role for miR-30a-3p in RCC progression which is potentially mediated via Wnt2.

摘要

已经对微小RNA(miR)-30a-3p在几种人类癌症中的表达和功能进行了研究。然而,miR-30a-3p在肾细胞癌(RCC)中的生物学功能仍不清楚。在本研究中,我们证明与相邻正常组织相比,miR-30a-3p在RCC组织中的表达下调。此外,miR-30a-3p的异位表达显著抑制了人RCC细胞系的增殖、迁移和侵袭,同时miR-30a-3p也抑制了肿瘤生长。TargetScan软件将Wnt2鉴定为miR-30a-3p的潜在直接靶点。为了证实这种关系,Wnt2被异位表达。随后miR-30a-3p对RCC细胞增殖和侵袭的影响得以恢复。因此,本研究结果支持miR-30a-3p在RCC进展中具有抗肿瘤作用,这可能是通过Wnt2介导的。