Cargando…

LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells

Liver cancer stem cells (CSCs) may contribute to the high rate of recurrence and heterogeneity of hepatocellular carcinoma (HCC). However, the biology of hepatic CSCs remains largely undefined. Through analysis of transcriptome microarray data, we identify a long noncoding RNA (lncRNA) called lncBRM...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Pingping, Wang, Yanying, Wu, Jiayi, Huang, Guanling, Liu, Benyu, Ye, Buqing, Du, Ying, Gao, Guangxia, Tian, Yong, He, Lei, Fan, Zusen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146280/
https://www.ncbi.nlm.nih.gov/pubmed/27905400
http://dx.doi.org/10.1038/ncomms13608
_version_ 1782473452879347712
author Zhu, Pingping
Wang, Yanying
Wu, Jiayi
Huang, Guanling
Liu, Benyu
Ye, Buqing
Du, Ying
Gao, Guangxia
Tian, Yong
He, Lei
Fan, Zusen
author_facet Zhu, Pingping
Wang, Yanying
Wu, Jiayi
Huang, Guanling
Liu, Benyu
Ye, Buqing
Du, Ying
Gao, Guangxia
Tian, Yong
He, Lei
Fan, Zusen
author_sort Zhu, Pingping
collection PubMed
description Liver cancer stem cells (CSCs) may contribute to the high rate of recurrence and heterogeneity of hepatocellular carcinoma (HCC). However, the biology of hepatic CSCs remains largely undefined. Through analysis of transcriptome microarray data, we identify a long noncoding RNA (lncRNA) called lncBRM, which is highly expressed in liver CSCs and HCC tumours. LncBRM is required for the self-renewal maintenance of liver CSCs and tumour initiation. In liver CSCs, lncBRM associates with BRM to initiate the BRG1/BRM switch and the BRG1-embedded BAF complex triggers activation of YAP1 signalling. Moreover, expression levels of lncBRM together with YAP1 signalling targets are positively correlated with tumour severity of HCC patients. Therefore, lncBRM and YAP1 signalling may serve as biomarkers for diagnosis and potential drug targets for HCC.
format Online
Article
Text
id pubmed-5146280
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-51462802016-12-23 LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells Zhu, Pingping Wang, Yanying Wu, Jiayi Huang, Guanling Liu, Benyu Ye, Buqing Du, Ying Gao, Guangxia Tian, Yong He, Lei Fan, Zusen Nat Commun Article Liver cancer stem cells (CSCs) may contribute to the high rate of recurrence and heterogeneity of hepatocellular carcinoma (HCC). However, the biology of hepatic CSCs remains largely undefined. Through analysis of transcriptome microarray data, we identify a long noncoding RNA (lncRNA) called lncBRM, which is highly expressed in liver CSCs and HCC tumours. LncBRM is required for the self-renewal maintenance of liver CSCs and tumour initiation. In liver CSCs, lncBRM associates with BRM to initiate the BRG1/BRM switch and the BRG1-embedded BAF complex triggers activation of YAP1 signalling. Moreover, expression levels of lncBRM together with YAP1 signalling targets are positively correlated with tumour severity of HCC patients. Therefore, lncBRM and YAP1 signalling may serve as biomarkers for diagnosis and potential drug targets for HCC. Nature Publishing Group 2016-12-01 /pmc/articles/PMC5146280/ /pubmed/27905400 http://dx.doi.org/10.1038/ncomms13608 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, Pingping
Wang, Yanying
Wu, Jiayi
Huang, Guanling
Liu, Benyu
Ye, Buqing
Du, Ying
Gao, Guangxia
Tian, Yong
He, Lei
Fan, Zusen
LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title_full LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title_fullStr LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title_full_unstemmed LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title_short LncBRM initiates YAP1 signalling activation to drive self-renewal of liver cancer stem cells
title_sort lncbrm initiates yap1 signalling activation to drive self-renewal of liver cancer stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146280/
https://www.ncbi.nlm.nih.gov/pubmed/27905400
http://dx.doi.org/10.1038/ncomms13608
work_keys_str_mv AT zhupingping lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT wangyanying lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT wujiayi lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT huangguanling lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT liubenyu lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT yebuqing lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT duying lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT gaoguangxia lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT tianyong lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT helei lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells
AT fanzusen lncbrminitiatesyap1signallingactivationtodriveselfrenewaloflivercancerstemcells