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微小RNA-429介导结直肠癌的肿瘤生长和转移。

miR-429 mediates tumor growth and metastasis in colorectal cancer.

作者信息

Han Yantao, Zhao Qian, Zhou Jie, Shi Rui

机构信息

Qingdao University Qingdao 266071, Shandong, China.

Qingdao University Affiliated Hospital Qingdao 266071, Shandong, China.

出版信息

Am J Cancer Res. 2017 Feb 1;7(2):218-233. eCollection 2017.

PMID:28337372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5336497/
Abstract

Colorectal cancer (CRC), presenting the third most common malignancy worldwide. In recent years, the aberrantly upregulation or downregulation of miRNAs in CRC have been evidenced in a number of studies. In this study, our results showed that the expression of miR-429 was significantly higher in CRC tissue compared with adjacent non-tumor tissue. In addition, our findings showed that miR-429 level was significantly associated with clinicoplathological features and prognosis of patients with CRC. Moreover, our findings showed that miR-429 exerted oncogenic effect by directly targeting HOXA5, a transcription factor of HOX families that is involved in the development and progression of CRC.

摘要

结直肠癌(CRC)是全球第三大常见恶性肿瘤。近年来,多项研究证实了CRC中miRNAs的异常上调或下调。在本研究中,我们的结果显示,与相邻非肿瘤组织相比,miR-429在CRC组织中的表达显著更高。此外,我们的研究结果表明,miR-429水平与CRC患者的临床病理特征和预后显著相关。而且,我们的研究结果表明,miR-429通过直接靶向HOXA5发挥致癌作用,HOXA5是HOX家族的一个转录因子,参与CRC的发生和发展。

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本文引用的文献

1
miR-429 is involved in regulation of NF-κBactivity by targeting IKKβ and suppresses oncogenic activity in cervical cancer cells.miR-429 通过靶向 IKKβ 参与 NF-κB 活性的调节,并抑制宫颈癌细胞的致癌活性。
FEBS Lett. 2017 Jan;591(1):118-128. doi: 10.1002/1873-3468.12502. Epub 2016 Dec 20.
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The Clinical Significance of MiR-429 as a Predictive Biomarker in Colorectal Cancer Patients Receiving 5-Fluorouracil Treatment.MiR-429作为接受5-氟尿嘧啶治疗的结直肠癌患者预测生物标志物的临床意义
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MiR-429 is linked to metastasis and poor prognosis in renal cell carcinoma by affecting epithelial-mesenchymal transition.MiR-429通过影响上皮-间质转化与肾细胞癌的转移及不良预后相关。
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miR-429 promotes the proliferation of non-small cell lung cancer cells via targeting DLC-1.微小RNA-429通过靶向DLC-1促进非小细胞肺癌细胞的增殖。
Oncol Lett. 2016 Sep;12(3):2163-2168. doi: 10.3892/ol.2016.4904. Epub 2016 Jul 22.
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Effect of evodiamine and berberine on miR-429 as an oncogene in human colorectal cancer.吴茱萸碱和小檗碱对作为人类结直肠癌致癌基因的miR-429的影响。
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Niclosamide inhibits colon cancer progression through downregulation of the Notch pathway and upregulation of the tumor suppressor miR-200 family.氯硝柳胺通过下调Notch信号通路和上调肿瘤抑制因子miR-200家族来抑制结肠癌进展。
Int J Mol Med. 2016 Sep;38(3):776-84. doi: 10.3892/ijmm.2016.2689. Epub 2016 Jul 22.
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HOXA5 determines cell fate transition and impedes tumor initiation and progression in breast cancer through regulation of E-cadherin and CD24.HOXA5通过调控E-钙黏蛋白和CD24来决定细胞命运转变,并抑制乳腺癌的起始和进展。
Oncogene. 2016 Oct 20;35(42):5539-5551. doi: 10.1038/onc.2016.95. Epub 2016 May 9.
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MiR-429 reverses epithelial-mesenchymal transition by restoring E-cadherin expression in bladder cancer.微小RNA-429通过恢复膀胱癌中E-钙黏蛋白的表达来逆转上皮-间质转化。
Oncotarget. 2016 May 3;7(18):26593-603. doi: 10.18632/oncotarget.8557.
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miR-429 functions as a tumor suppressor by targeting FSCN1 in gastric cancer cells.在胃癌细胞中,miR-429通过靶向FSCN1发挥肿瘤抑制作用。
Onco Targets Ther. 2016 Mar 3;9:1123-33. doi: 10.2147/OTT.S91879. eCollection 2016.
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HOXA5 Counteracts Stem Cell Traits by Inhibiting Wnt Signaling in Colorectal Cancer.HOXA5 通过抑制结直肠癌中的 Wnt 信号通路来拮抗干细胞特性。
Cancer Cell. 2015 Dec 14;28(6):815-829. doi: 10.1016/j.ccell.2015.11.001.