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Review Article | Open Access

MicroRNA-9 as a paradoxical but critical regulator of cancer metastasis: Implications in personalized medicine

Yichen Liua,b,1Qiong Zhaob,1Tao XibLufeng Zhengb( )Xiaoman Lia( )
Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province, 210023, PR China
School of Life Science and Technology, Jiangsu Key Laboratory of Carcinogenesis and Intervention, China Pharmaceutical University, 639 Longmian Road, Nanjing, Jiangsu Province, 211198, PR China

Peer review under responsibility of Chongqing Medical University.1 These authors contributed to this work equally.

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Abstract

Metastasis, is a development of secondary tumor growths at a distance from the primary site, and closely related to poor prognosis and mortality. However, there is still no effective treatment for metastatic cancer. Therefore, there is an urgent need to find an effective therapy for cancer metastasis. Plenty of evidence indicates that miR-9 can function as a promoter or suppressor in cancer metastasis and coordinate multistep of metastatic process. In this review, we summarize the different roles of miR-9 with the corresponding molecular mechanisms in metastasis of twelve common cancers and the multiple mechanisms underlying miR-9-mediated regulation of metastasis, benefiting the further research of miR-9 and metastasis, and hoping to bridge it with clinical applications.

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Genes & Diseases
Pages 759-768

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Cite this article:
Liu Y, Zhao Q, Xi T, et al. MicroRNA-9 as a paradoxical but critical regulator of cancer metastasis: Implications in personalized medicine. Genes & Diseases, 2021, 8(6): 759-768. https://doi.org/10.1016/j.gendis.2020.10.005

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Received: 15 June 2020
Revised: 27 September 2020
Accepted: 18 October 2020
Published: 23 October 2020
© 2020, Chongqing Medical University. Production and hosting by Elsevier B.V.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).