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Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma

The aim of our study is to explore the regulation of C1QTNF1-AS1 on its target miR-221-3p/SOCS3 in human hepatocellular carcinoma (HCC). To explore the underlying molecular regulation of non-coding RNA for HCC, differentially expressed patterns of lncRNAs and genes were examined by RNA-seq. GO and K...

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Autores principales: Han, Weijie, Yu, Guofeng, Meng, Xianmei, Hong, Hong, Zheng, Liansheng, Wu, Xiaobo, Zhang, Dongsheng, Yan, Boshi, Ma, Yongqiang, Li, Xiaolong, Wang, Qiuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745033/
https://www.ncbi.nlm.nih.gov/pubmed/31222560
http://dx.doi.org/10.1007/s11010-019-03569-w
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author Han, Weijie
Yu, Guofeng
Meng, Xianmei
Hong, Hong
Zheng, Liansheng
Wu, Xiaobo
Zhang, Dongsheng
Yan, Boshi
Ma, Yongqiang
Li, Xiaolong
Wang, Qiuhong
author_facet Han, Weijie
Yu, Guofeng
Meng, Xianmei
Hong, Hong
Zheng, Liansheng
Wu, Xiaobo
Zhang, Dongsheng
Yan, Boshi
Ma, Yongqiang
Li, Xiaolong
Wang, Qiuhong
author_sort Han, Weijie
collection PubMed
description The aim of our study is to explore the regulation of C1QTNF1-AS1 on its target miR-221-3p/SOCS3 in human hepatocellular carcinoma (HCC). To explore the underlying molecular regulation of non-coding RNA for HCC, differentially expressed patterns of lncRNAs and genes were examined by RNA-seq. GO and KEGG pathway analysis were done based on the function of mRNAs that mediated by differentially expressed lncRNAs. RT-qPCR and western blot were conducted to detect the mRNA and protein level expression of C1QTNF1-AS1, miR-221-3p, SOCS3 and key proteins in JAK/STAT signaling pathway in HCC tissues and cells. The target miRNA of differentially expressed C1QTNF1-AS1 and SOCS3 was miR-221-3p predicted by bioinformatics analysis. C1QTNF1-AS1 and SOCS3 was downregulated and miR-221-3p was upregulated in HCC tissues and cells. In HepG2 and Huh-7 cells, the overexpression of C1QTNF1-AS1 or SOCS3, and silencing of miR-221-3p inhibited proliferation, migration, invasion and JAK/STAT signaling pathway, while promoted cell apoptosis. The results of dual-luciferase assay indicated that C1QTNF1-AS1 regulated miR-221-3p and miR-221-3p targeted SOCS3 by directly binding. And the growth of HCC in vivo was impeded when C1QTNF1-AS1 was upregulated. Overexpression of C1QTNF1-AS1 could downregulate miR-221-3p thereby inhibited the proliferation, migration and invasion of HCC cells.
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spelling pubmed-67450332019-09-27 Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma Han, Weijie Yu, Guofeng Meng, Xianmei Hong, Hong Zheng, Liansheng Wu, Xiaobo Zhang, Dongsheng Yan, Boshi Ma, Yongqiang Li, Xiaolong Wang, Qiuhong Mol Cell Biochem Article The aim of our study is to explore the regulation of C1QTNF1-AS1 on its target miR-221-3p/SOCS3 in human hepatocellular carcinoma (HCC). To explore the underlying molecular regulation of non-coding RNA for HCC, differentially expressed patterns of lncRNAs and genes were examined by RNA-seq. GO and KEGG pathway analysis were done based on the function of mRNAs that mediated by differentially expressed lncRNAs. RT-qPCR and western blot were conducted to detect the mRNA and protein level expression of C1QTNF1-AS1, miR-221-3p, SOCS3 and key proteins in JAK/STAT signaling pathway in HCC tissues and cells. The target miRNA of differentially expressed C1QTNF1-AS1 and SOCS3 was miR-221-3p predicted by bioinformatics analysis. C1QTNF1-AS1 and SOCS3 was downregulated and miR-221-3p was upregulated in HCC tissues and cells. In HepG2 and Huh-7 cells, the overexpression of C1QTNF1-AS1 or SOCS3, and silencing of miR-221-3p inhibited proliferation, migration, invasion and JAK/STAT signaling pathway, while promoted cell apoptosis. The results of dual-luciferase assay indicated that C1QTNF1-AS1 regulated miR-221-3p and miR-221-3p targeted SOCS3 by directly binding. And the growth of HCC in vivo was impeded when C1QTNF1-AS1 was upregulated. Overexpression of C1QTNF1-AS1 could downregulate miR-221-3p thereby inhibited the proliferation, migration and invasion of HCC cells. Springer US 2019-06-06 2019 /pmc/articles/PMC6745033/ /pubmed/31222560 http://dx.doi.org/10.1007/s11010-019-03569-w Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Han, Weijie
Yu, Guofeng
Meng, Xianmei
Hong, Hong
Zheng, Liansheng
Wu, Xiaobo
Zhang, Dongsheng
Yan, Boshi
Ma, Yongqiang
Li, Xiaolong
Wang, Qiuhong
Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title_full Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title_fullStr Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title_full_unstemmed Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title_short Potential of C1QTNF1-AS1 regulation in human hepatocellular carcinoma
title_sort potential of c1qtnf1-as1 regulation in human hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745033/
https://www.ncbi.nlm.nih.gov/pubmed/31222560
http://dx.doi.org/10.1007/s11010-019-03569-w
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