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miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway

The Wnt/β-catenin signalling pathway is known to play a vital role in the maintenance of cancer stem cells (CSCs), which are reported to be the origine of malignant cancers, and result in poor prognosis of multiple kinds of cancer. Therefore, it is of great importance to illuminate the mechanism by...

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Autores principales: Ge, Chunlei, Wu, Shikai, Wang, Weiwei, Liu, Zhimin, Zhang, Jianhua, Wang, Zhenyu, Li, Ruilei, Zhang, Zhiwei, Li, Zhen, Dong, Suwei, Wang, Ying, Xue, Yuanbo, Yang, Jinyan, Tan, Qinghua, Wang, Ziping, Song, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484432/
https://www.ncbi.nlm.nih.gov/pubmed/25844602
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author Ge, Chunlei
Wu, Shikai
Wang, Weiwei
Liu, Zhimin
Zhang, Jianhua
Wang, Zhenyu
Li, Ruilei
Zhang, Zhiwei
Li, Zhen
Dong, Suwei
Wang, Ying
Xue, Yuanbo
Yang, Jinyan
Tan, Qinghua
Wang, Ziping
Song, Xin
author_facet Ge, Chunlei
Wu, Shikai
Wang, Weiwei
Liu, Zhimin
Zhang, Jianhua
Wang, Zhenyu
Li, Ruilei
Zhang, Zhiwei
Li, Zhen
Dong, Suwei
Wang, Ying
Xue, Yuanbo
Yang, Jinyan
Tan, Qinghua
Wang, Ziping
Song, Xin
author_sort Ge, Chunlei
collection PubMed
description The Wnt/β-catenin signalling pathway is known to play a vital role in the maintenance of cancer stem cells (CSCs), which are reported to be the origine of malignant cancers, and result in poor prognosis of multiple kinds of cancer. Therefore, it is of great importance to illuminate the mechanism by which the Wnt/β-catenin pathway regulates the cancer stem cell-like traits in cancers. Here, we report that miR-942 is significantly upregulated in esophageal squamous cell carcinoma (ESCC), and miR-942 levels are associated with poor prognosis in ESCC patients. Overexpression of miR-942 promotes, whereas inhibition of miR-942 decreases, the tumor sphere formation, the CD90(+) subpopulation cells and the expression of pluripotency associated markers. Moreover, in vivo assay shows that miR-942 overexpressing cells form larger tumors and display higher tumourigenesis. Furthermore, we demonstrate that miR-942 upregulates the Wnt/β-catenin signaling activity via directly targeting sFRP4, GSK3β and TLE1, which are multiple level negative regulators of the Wnt/β-catenin signaling cascade. In addition, our results indicate that c-myc directly binds to the miR-942 promoter and promotes its expression. Taken together, our findings establish an oncogenic role of miR-942 in ESCC and indicate that miR-942 might be an effective therapeutic target for ESCC.
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spelling pubmed-44844322015-07-10 miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway Ge, Chunlei Wu, Shikai Wang, Weiwei Liu, Zhimin Zhang, Jianhua Wang, Zhenyu Li, Ruilei Zhang, Zhiwei Li, Zhen Dong, Suwei Wang, Ying Xue, Yuanbo Yang, Jinyan Tan, Qinghua Wang, Ziping Song, Xin Oncotarget Research Paper The Wnt/β-catenin signalling pathway is known to play a vital role in the maintenance of cancer stem cells (CSCs), which are reported to be the origine of malignant cancers, and result in poor prognosis of multiple kinds of cancer. Therefore, it is of great importance to illuminate the mechanism by which the Wnt/β-catenin pathway regulates the cancer stem cell-like traits in cancers. Here, we report that miR-942 is significantly upregulated in esophageal squamous cell carcinoma (ESCC), and miR-942 levels are associated with poor prognosis in ESCC patients. Overexpression of miR-942 promotes, whereas inhibition of miR-942 decreases, the tumor sphere formation, the CD90(+) subpopulation cells and the expression of pluripotency associated markers. Moreover, in vivo assay shows that miR-942 overexpressing cells form larger tumors and display higher tumourigenesis. Furthermore, we demonstrate that miR-942 upregulates the Wnt/β-catenin signaling activity via directly targeting sFRP4, GSK3β and TLE1, which are multiple level negative regulators of the Wnt/β-catenin signaling cascade. In addition, our results indicate that c-myc directly binds to the miR-942 promoter and promotes its expression. Taken together, our findings establish an oncogenic role of miR-942 in ESCC and indicate that miR-942 might be an effective therapeutic target for ESCC. Impact Journals LLC 2015-03-30 /pmc/articles/PMC4484432/ /pubmed/25844602 Text en Copyright: © 2015 Ge et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ge, Chunlei
Wu, Shikai
Wang, Weiwei
Liu, Zhimin
Zhang, Jianhua
Wang, Zhenyu
Li, Ruilei
Zhang, Zhiwei
Li, Zhen
Dong, Suwei
Wang, Ying
Xue, Yuanbo
Yang, Jinyan
Tan, Qinghua
Wang, Ziping
Song, Xin
miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title_full miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title_fullStr miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title_full_unstemmed miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title_short miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathway
title_sort mir-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of wnt/β-catenin signalling pathway
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484432/
https://www.ncbi.nlm.nih.gov/pubmed/25844602
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