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Advances in prognostic and therapeutic targets for hepatocellular carcinoma and intrahepatic cholangiocarcinoma: The hippo signaling pathway.肝细胞癌和肝内胆管癌的预后及治疗靶点研究进展:河马信号通路
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MiR-186-3p attenuates tumorigenesis of cervical cancer by targeting IGF1.miR-186-3p 通过靶向 IGF1 抑制宫颈癌的发生。
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Upregulated microRNA let-7a accelerates apoptosis and inhibits proliferation in uterine junctional zone smooth muscle cells in adenomyosis under conditions of a normal activated hippo-YAP1 axis.上调的 microRNA let-7a 在正常激活的 hippo-YAP1 轴条件下加速子宫交界区平滑肌细胞的凋亡并抑制其增殖,从而导致子宫腺肌病。
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COL4A1, negatively regulated by XPD and miR-29a-3p, promotes cell proliferation, migration, invasion and epithelial-mesenchymal transition in liver cancer cells.COL4A1受XPD和miR-29a-3p负调控,促进肝癌细胞的增殖、迁移、侵袭及上皮-间质转化。
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本文引用的文献

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The Hippo signaling pathway in liver regeneration and tumorigenesis.肝脏再生与肿瘤发生中的河马信号通路。
Acta Biochim Biophys Sin (Shanghai). 2015 Jan;47(1):46-52. doi: 10.1093/abbs/gmu106. Epub 2014 Dec 4.
2
Targeting Hippo pathway by specific interruption of YAP-TEAD interaction using cyclic YAP-like peptides.靶向 Hippo 通路通过使用环状 YAP 样肽特异性阻断 YAP-TEAD 相互作用。
FASEB J. 2015 Feb;29(2):724-32. doi: 10.1096/fj.14-262980. Epub 2014 Nov 10.
3
Plasma microRNA-186 and proteinuria in focal segmental glomerulosclerosis.局灶节段性肾小球硬化症中的血浆 microRNA-186 和蛋白尿。
Am J Kidney Dis. 2015 Feb;65(2):223-32. doi: 10.1053/j.ajkd.2014.07.013. Epub 2014 Sep 11.
4
YAP activation is an early event and a potential therapeutic target in liver cancer development.YAP 激活是肝癌发展中的早期事件和潜在治疗靶点。
J Hepatol. 2014 Nov;61(5):1088-96. doi: 10.1016/j.jhep.2014.06.033. Epub 2014 Jul 7.
5
Predicted overlapping microRNA regulators of acetylcholine packaging and degradation in neuroinflammation-related disorders.预测神经炎症相关疾病中乙酰胆碱包装和降解的重叠 microRNA 调控因子。
Front Mol Neurosci. 2014 Feb 10;7:9. doi: 10.3389/fnmol.2014.00009. eCollection 2014.
6
miR-186, miR-3651 and miR-494: potential biomarkers for oral squamous cell carcinoma extracted from whole blood.miR-186、miR-3651和miR-494:从全血中提取的口腔鳞状细胞癌潜在生物标志物。
Oncol Rep. 2014 Mar;31(3):1429-36. doi: 10.3892/or.2014.2983. Epub 2014 Jan 20.
7
miR-186 inhibits muscle cell differentiation through myogenin regulation.miR-186 通过调节肌生成蛋白抑制肌肉细胞分化。
J Biol Chem. 2014 Feb 14;289(7):3923-35. doi: 10.1074/jbc.M113.507343. Epub 2014 Jan 2.
8
The hippo-yes association protein pathway in liver cancer.肝癌中的河马样激酶-Yes 关联蛋白通路。
Gastroenterol Res Pract. 2013;2013:187070. doi: 10.1155/2013/187070. Epub 2013 Aug 6.
9
PTTG1 promotes migration and invasion of human non-small cell lung cancer cells and is modulated by miR-186.PTTG1 促进人非小细胞肺癌细胞的迁移和侵袭,并受 miR-186 调节。
Carcinogenesis. 2013 Sep;34(9):2145-55. doi: 10.1093/carcin/bgt158. Epub 2013 May 13.
10
Structures of YAP protein domains reveal promising targets for development of new cancer drugs.YAP 蛋白结构域的结构为开发新的癌症药物提供了有希望的靶点。
Semin Cell Dev Biol. 2012 Sep;23(7):827-33. doi: 10.1016/j.semcdb.2012.05.002. Epub 2012 May 17.

微小RNA-186靶向Yes相关蛋白1以抑制肝细胞癌中的Hippo信号通路和肿瘤发生。

MicroRNA-186 targets Yes-associated protein 1 to inhibit Hippo signaling and tumorigenesis in hepatocellular carcinoma.

作者信息

Ruan Tingyan, He Xiaoting, Yu Jun, Hang Zhiqiang

机构信息

Department of Oncology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, Jiangsu 214023, P.R. China.

Department of Thoracic Surgery, The Second People's Hospital of Wuxi, Wuxi, Jiangsu 214002, P.R. China.

出版信息

Oncol Lett. 2016 Apr;11(4):2941-2945. doi: 10.3892/ol.2016.4312. Epub 2016 Mar 8.

DOI:10.3892/ol.2016.4312
PMID:27073580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4812570/
Abstract

Liver cancer, particularly hepatocellular carcinoma (HCC), is one of leading causes of cancer-related mortality worldwide. Upregulation of the evolutionary conserved Hippo signaling pathway has been observed in HCC patients, and Yes-associated protein 1 (YAP1) has been reported to play a key role in HCC tumorigenesis. microRNAs (miRNAs) are a family of small non-coding RNAs, usually 21-25 nucleotides in length, and are essential in the regulation of gene expression. Abnormal miRNA expression has been implicated in the initiation and progression of numerous forms of cancers, including liver cancer. Here, we report the identification of a novel miRNA, miR-186, and its functions as an HCC tumor suppressor. We observed that miR-186 was downregulated in several HCC cell lines, and that it directly targets YAP1 mRNA. Overexpression of miR-186 in HCC cells significantly downregulates YAP1 mRNA and protein levels, leading to downregulation of the Hippo signaling pathway, which in turn severely inhibits HCC cell migration, invasion and proliferation. Our study is the first to report the direct involvement of miR-186 in downregulating YAP1 and, more significantly, inhibiting HCC tumorigenesis, and supports the role miR-186 as a potential therapeutic target in treating liver cancer.

摘要

肝癌,尤其是肝细胞癌(HCC),是全球癌症相关死亡的主要原因之一。在HCC患者中观察到进化保守的Hippo信号通路上调,并且据报道Yes相关蛋白1(YAP1)在HCC肿瘤发生中起关键作用。微小RNA(miRNA)是一类小的非编码RNA,通常长度为21 - 25个核苷酸,在基因表达调控中至关重要。miRNA表达异常与包括肝癌在内的多种癌症的发生和发展有关。在此,我们报告了一种新型miRNA miR - 186的鉴定及其作为HCC肿瘤抑制因子的功能。我们观察到miR - 186在几种HCC细胞系中表达下调,并且它直接靶向YAP1 mRNA。在HCC细胞中过表达miR - 186显著下调YAP1 mRNA和蛋白水平,导致Hippo信号通路下调,进而严重抑制HCC细胞的迁移、侵袭和增殖。我们的研究首次报道了miR - 186直接参与下调YAP1,更重要的是,抑制HCC肿瘤发生,并支持miR - 186作为治疗肝癌的潜在治疗靶点的作用。