MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF

MicroRNAs (miRNAs) have vastly expanded our view of RNA world in intracellular signal regulating networks. Here, we functionally characterized a normally highly expressed miRNA, miR-30a-5p (MIMAT0000087), which exhibits downregulated expression profiles in prostate cancer samples. MiR-30a-5p knockdo...

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Main Authors: Hu Zhao, Wei Zhang, Xiaofeng Lai, Hehuan Zhu, Shenhang Zhang, Weizhen Wu, Shuiliang Wang, Minying Tang, Zhen Deng, Jianming Tan
Format: Article
Language:English
Published: Taylor & Francis Group 2019-12-01
Series:Artificial Cells, Nanomedicine, and Biotechnology
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/21691401.2018.1553783
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author Hu Zhao
Wei Zhang
Xiaofeng Lai
Hehuan Zhu
Shenhang Zhang
Weizhen Wu
Shuiliang Wang
Minying Tang
Zhen Deng
Jianming Tan
author_facet Hu Zhao
Wei Zhang
Xiaofeng Lai
Hehuan Zhu
Shenhang Zhang
Weizhen Wu
Shuiliang Wang
Minying Tang
Zhen Deng
Jianming Tan
author_sort Hu Zhao
collection DOAJ
description MicroRNAs (miRNAs) have vastly expanded our view of RNA world in intracellular signal regulating networks. Here, we functionally characterized a normally highly expressed miRNA, miR-30a-5p (MIMAT0000087), which exhibits downregulated expression profiles in prostate cancer samples. MiR-30a-5p knockdown and overexpression in PC-3 cell line alters cell proliferation supporting a tumour suppressor role. We also discovered that PCLAF is the direct target of miR-30a-5p. Notably, PC-3 cell proliferation is inhibited by miR-30a-5p/PCLAF axis. miR-30a-5p represents a novel molecule of functionally important miRNAs which may shed light on the novel therapeutic targets for prostate cancer.
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spelling doaj.art-e7cf2983653a46b486d5a5a3de47cf7f2022-12-22T02:25:41ZengTaylor & Francis GroupArtificial Cells, Nanomedicine, and Biotechnology2169-14012169-141X2019-12-0147127828910.1080/21691401.2018.1553783MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAFHu Zhao0Wei Zhang1Xiaofeng Lai2Hehuan Zhu3Shenhang Zhang4Weizhen Wu5Shuiliang Wang6Minying Tang7Zhen Deng8Jianming Tan9Fujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaDepartment of Urology, Bayi Hospital affiliated Nanjing University of Chinese Medicine, Nanjing, P. R. ChinaDepartment of Clinical Genetics and Experimental Medicine, 900 Hospital of the Joint Logistics Team, Xiamen University School of Medicine, Fuzhou, Fujian, P. R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaChinaFujian Key Laboratory of Exercise Rehabilitation, College of Rehabilitation Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian, P. R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaFujian Provincial Key Laboratory of Transplant Biology, Fuzhou Dongfang Hospital of Xiamen University (900 Hospital of the Joint Logistics Team), Fuzhou, Fujian, P.R. ChinaMicroRNAs (miRNAs) have vastly expanded our view of RNA world in intracellular signal regulating networks. Here, we functionally characterized a normally highly expressed miRNA, miR-30a-5p (MIMAT0000087), which exhibits downregulated expression profiles in prostate cancer samples. MiR-30a-5p knockdown and overexpression in PC-3 cell line alters cell proliferation supporting a tumour suppressor role. We also discovered that PCLAF is the direct target of miR-30a-5p. Notably, PC-3 cell proliferation is inhibited by miR-30a-5p/PCLAF axis. miR-30a-5p represents a novel molecule of functionally important miRNAs which may shed light on the novel therapeutic targets for prostate cancer.https://www.tandfonline.com/doi/10.1080/21691401.2018.1553783MiR-30a-5pprostate cancerPCLAFproliferation
spellingShingle Hu Zhao
Wei Zhang
Xiaofeng Lai
Hehuan Zhu
Shenhang Zhang
Weizhen Wu
Shuiliang Wang
Minying Tang
Zhen Deng
Jianming Tan
MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
Artificial Cells, Nanomedicine, and Biotechnology
MiR-30a-5p
prostate cancer
PCLAF
proliferation
title MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
title_full MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
title_fullStr MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
title_full_unstemmed MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
title_short MiR-30a-5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting PCLAF
title_sort mir 30a 5p frequently downregulated in prostate cancer inhibits cell proliferation via targeting pclaf
topic MiR-30a-5p
prostate cancer
PCLAF
proliferation
url https://www.tandfonline.com/doi/10.1080/21691401.2018.1553783
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