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MicroRNA-449a maintains self-renewal in liver cancer stem-like cells by targeting Tcf3.


ABSTRACT: Cancer stem cells (CSCs) are thought to be responsible for tumor invasion, metastasis, and recurrence. We previously showed that the pluripotency factor Nanog not only serves as a novel biomarker of CSCs but also potentially plays a crucial role in maintaining the self-renewal ability of liver CSCs. However, how CSCs maintain Nanog gene expression has not been elucidated. Here, we demonstrated that microRNA-449a (miR-449a) is overexpressed in poorly differentiated hepatocellular carcinoma tissues, drug-resistant liver cancer cells, cultured liver tumorspheres, and Nanog-positive liver cancer cells. The upregulation of miR-449a in non-CSCs increased stemness, whereas the downregulation of miR-449a in Nanog-positive CSCs reduced stemness. Furthermore, transcription factor 3 (TCF3), a target of miR-449a, could downregulate Nanog expression, and restoring TCF3 expression in miR-449a-expressing Nanog-negative cells abrogated cellular stemness. These data establish that the miR449a-TCF3-Nanog axis maintains stemness in liver CSCs.

SUBMITTER: Zhang Q 

PROVIDER: S-EPMC5746375 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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MicroRNA-449a maintains self-renewal in liver cancer stem-like cells by targeting <i>Tcf3</i>.

Zhang Qianzhen Q   Yang Zhi Z   Shan Juanjuan J   Liu Limei L   Liu Chungang C   Shen Junjie J   Chen Xuejiao X   Xu Yanmin Y   Chen Jun J   Ma Qinghua Q   Yang Li L   Qian Cheng C  

Oncotarget 20171127 66


Cancer stem cells (CSCs) are thought to be responsible for tumor invasion, metastasis, and recurrence. We previously showed that the pluripotency factor Nanog not only serves as a novel biomarker of CSCs but also potentially plays a crucial role in maintaining the self-renewal ability of liver CSCs. However, how CSCs maintain <i>Nanog</i> gene expression has not been elucidated. Here, we demonstrated that microRNA-449a (miR-449a) is overexpressed in poorly differentiated hepatocellular carcinoma  ...[more]

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