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...

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Veröffentlicht in:Nature communications 2016-12, Vol.7 (1), p.13608-13608, Article 13608
Hauptverfasser: Zhu, Pingping, Wang, Yanying, Wu, Jiayi, Huang, Guanling, Liu, Benyu, Ye, Buqing, Du, Ying, Gao, Guangxia, Tian, Yong, He, Lei, Fan, Zusen
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Sprache:eng
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Zusammenfassung: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. Liver cancer stem cells (CSCs) may contribute to the high rate of recurrence of hepatocellular carcinoma. Here, the authors show that the long coding RNA, LcnBRM , regulates the self-renewal of liver CSCs and tumour initiation through binding to BAF complex thereby activating YAP1.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms13608