Cargando…

Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma

Long non‐coding RNAs (lncRNAs) play essential roles in diverse biological processes; however, current understanding of the mechanism underlying the regulation of tumour proliferation and metastasis is limited. Lung cancer‐associated transcript 1 (LUCAT1) has been reported in a variety of human cance...

Descripción completa

Detalles Bibliográficos
Autores principales: Lou, Yun, Yu, Yue, Xu, Xiaolia, Zhou, Shu, Shen, Haiyuan, Fan, Tianlong, Wu, Di, Yin, Jie, Li, Guoqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378214/
https://www.ncbi.nlm.nih.gov/pubmed/30588744
http://dx.doi.org/10.1111/jcmm.14088
_version_ 1783395887562620928
author Lou, Yun
Yu, Yue
Xu, Xiaolia
Zhou, Shu
Shen, Haiyuan
Fan, Tianlong
Wu, Di
Yin, Jie
Li, Guoqiang
author_facet Lou, Yun
Yu, Yue
Xu, Xiaolia
Zhou, Shu
Shen, Haiyuan
Fan, Tianlong
Wu, Di
Yin, Jie
Li, Guoqiang
author_sort Lou, Yun
collection PubMed
description Long non‐coding RNAs (lncRNAs) play essential roles in diverse biological processes; however, current understanding of the mechanism underlying the regulation of tumour proliferation and metastasis is limited. Lung cancer‐associated transcript 1 (LUCAT1) has been reported in a variety of human cancers, while its role in hepatocellular carcinoma (HCC) remains unclear. This study aimed to determine the biological role and underlying mechanism of LUCAT1 on progression and metastasis in HCC cells and clinical specimens. Our results demonstrated that LUCAT1 was up‐regulated in HCC tissues and cells. Loss‐ and gain‐of‐function studies revealed that LUCAT1 promotes the proliferation and metastasis of HCC cells in vitro and in vivo. Furthermore, RNA pulldown and Western blot assays indicated that LUCAT1 inhibited the phosphorylation of Annexin A2 (ANXA2) to reduce the degradation of ANXA2‐S100A10 heterotetramer (AIIt), which in turn accelerated the secretion of plasminogen into plasmin, thereby resulting in the activation of metalloprotease proteins. In conclusion, we propose that LUCAT1 serves as a novel diagnostic and therapeutic target for HCC.
format Online
Article
Text
id pubmed-6378214
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-63782142019-03-01 Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma Lou, Yun Yu, Yue Xu, Xiaolia Zhou, Shu Shen, Haiyuan Fan, Tianlong Wu, Di Yin, Jie Li, Guoqiang J Cell Mol Med Original Articles Long non‐coding RNAs (lncRNAs) play essential roles in diverse biological processes; however, current understanding of the mechanism underlying the regulation of tumour proliferation and metastasis is limited. Lung cancer‐associated transcript 1 (LUCAT1) has been reported in a variety of human cancers, while its role in hepatocellular carcinoma (HCC) remains unclear. This study aimed to determine the biological role and underlying mechanism of LUCAT1 on progression and metastasis in HCC cells and clinical specimens. Our results demonstrated that LUCAT1 was up‐regulated in HCC tissues and cells. Loss‐ and gain‐of‐function studies revealed that LUCAT1 promotes the proliferation and metastasis of HCC cells in vitro and in vivo. Furthermore, RNA pulldown and Western blot assays indicated that LUCAT1 inhibited the phosphorylation of Annexin A2 (ANXA2) to reduce the degradation of ANXA2‐S100A10 heterotetramer (AIIt), which in turn accelerated the secretion of plasminogen into plasmin, thereby resulting in the activation of metalloprotease proteins. In conclusion, we propose that LUCAT1 serves as a novel diagnostic and therapeutic target for HCC. John Wiley and Sons Inc. 2018-12-26 2019-03 /pmc/articles/PMC6378214/ /pubmed/30588744 http://dx.doi.org/10.1111/jcmm.14088 Text en © 2018 The Authors Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Lou, Yun
Yu, Yue
Xu, Xiaolia
Zhou, Shu
Shen, Haiyuan
Fan, Tianlong
Wu, Di
Yin, Jie
Li, Guoqiang
Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title_full Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title_fullStr Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title_full_unstemmed Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title_short Long non‐coding RNA LUCAT1 promotes tumourigenesis by inhibiting ANXA2 phosphorylation in hepatocellular carcinoma
title_sort long non‐coding rna lucat1 promotes tumourigenesis by inhibiting anxa2 phosphorylation in hepatocellular carcinoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378214/
https://www.ncbi.nlm.nih.gov/pubmed/30588744
http://dx.doi.org/10.1111/jcmm.14088
work_keys_str_mv AT louyun longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT yuyue longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT xuxiaolia longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT zhoushu longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT shenhaiyuan longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT fantianlong longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT wudi longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT yinjie longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma
AT liguoqiang longnoncodingrnalucat1promotestumourigenesisbyinhibitinganxa2phosphorylationinhepatocellularcarcinoma