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MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway
The decrease of microRNA-452 (miR-452) in gliomas promoted stem-like features and tumorigenesis. However, the role of miR-452, especially in regulating cancer stem cells (CSCs) in hepatocellular carcinoma (HCC) remains ambiguous. We enriched stem-like HCC cells by serial passages of hepatospheres wi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053705/ https://www.ncbi.nlm.nih.gov/pubmed/27058905 http://dx.doi.org/10.18632/oncotarget.8584 |
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author | Zheng, Zhiyun Liu, Jimin Yang, Zhe Wu, Limin Xie, Haiyang Jiang, Chaozhe Lin, Binyi Chen, Tianchi Xing, Chunyang Liu, Zhikun Song, Penghong Yin, Shengyong Zheng, Shusen Zhou, Lin |
author_facet | Zheng, Zhiyun Liu, Jimin Yang, Zhe Wu, Limin Xie, Haiyang Jiang, Chaozhe Lin, Binyi Chen, Tianchi Xing, Chunyang Liu, Zhikun Song, Penghong Yin, Shengyong Zheng, Shusen Zhou, Lin |
author_sort | Zheng, Zhiyun |
collection | PubMed |
description | The decrease of microRNA-452 (miR-452) in gliomas promoted stem-like features and tumorigenesis. However, the role of miR-452, especially in regulating cancer stem cells (CSCs) in hepatocellular carcinoma (HCC) remains ambiguous. We enriched stem-like HCC cells by serial passages of hepatospheres with chemotherapeutic agents. Stem-like characteristics including the capabilities of chemo-resistance, stemness-related gene expression profiling, self-renewal, tumorigenicity and metastasis formation were detected. MiR-452 was markedly increased in the chemo-resistant hepatospheres and human HCC tissues. and the overexpression of miR-452 in HCC patients predicted poor overall survival. MiR-452 significantly promoted stem-like characteristics in vitro and in vivo. Further, Sox7 was identified as the direct target of miR-452, which could physically bind with β-catenin and TCF4 in the nucleus and then inhibit the activity of Wnt/β-catenin signaling pathway. Finally, the combined chemotherapy of doxorubicin and all-trans retinoic acid (ATRA) showed dramatically efficiency in suppressing HCC metastasis. These data suggested that miR-452 promoted stem-like traits of HCC, which might be a potential therapeutic target for HCC. The combination of doxorubicin and ATRA might be a promising therapy in HCC management. |
format | Online Article Text |
id | pubmed-5053705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50537052016-10-12 MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway Zheng, Zhiyun Liu, Jimin Yang, Zhe Wu, Limin Xie, Haiyang Jiang, Chaozhe Lin, Binyi Chen, Tianchi Xing, Chunyang Liu, Zhikun Song, Penghong Yin, Shengyong Zheng, Shusen Zhou, Lin Oncotarget Research Paper The decrease of microRNA-452 (miR-452) in gliomas promoted stem-like features and tumorigenesis. However, the role of miR-452, especially in regulating cancer stem cells (CSCs) in hepatocellular carcinoma (HCC) remains ambiguous. We enriched stem-like HCC cells by serial passages of hepatospheres with chemotherapeutic agents. Stem-like characteristics including the capabilities of chemo-resistance, stemness-related gene expression profiling, self-renewal, tumorigenicity and metastasis formation were detected. MiR-452 was markedly increased in the chemo-resistant hepatospheres and human HCC tissues. and the overexpression of miR-452 in HCC patients predicted poor overall survival. MiR-452 significantly promoted stem-like characteristics in vitro and in vivo. Further, Sox7 was identified as the direct target of miR-452, which could physically bind with β-catenin and TCF4 in the nucleus and then inhibit the activity of Wnt/β-catenin signaling pathway. Finally, the combined chemotherapy of doxorubicin and all-trans retinoic acid (ATRA) showed dramatically efficiency in suppressing HCC metastasis. These data suggested that miR-452 promoted stem-like traits of HCC, which might be a potential therapeutic target for HCC. The combination of doxorubicin and ATRA might be a promising therapy in HCC management. Impact Journals LLC 2016-04-05 /pmc/articles/PMC5053705/ /pubmed/27058905 http://dx.doi.org/10.18632/oncotarget.8584 Text en Copyright: © 2016 Zheng 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 Zheng, Zhiyun Liu, Jimin Yang, Zhe Wu, Limin Xie, Haiyang Jiang, Chaozhe Lin, Binyi Chen, Tianchi Xing, Chunyang Liu, Zhikun Song, Penghong Yin, Shengyong Zheng, Shusen Zhou, Lin MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title | MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title_full | MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title_fullStr | MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title_full_unstemmed | MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title_short | MicroRNA-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting Sox7 involving Wnt/β-catenin signaling pathway |
title_sort | microrna-452 promotes stem-like cells of hepatocellular carcinoma by inhibiting sox7 involving wnt/β-catenin signaling pathway |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053705/ https://www.ncbi.nlm.nih.gov/pubmed/27058905 http://dx.doi.org/10.18632/oncotarget.8584 |
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