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Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN
Maternally expressed gene 3 (MEG3) encodes an lncRNA which is suggested to function as a tumor suppressor and has been showed to involve in a variety of cancers. Herein, our findings demonstrate that MEG3 inhibits the malignant progression of liver cancer cells in vitro and in vivo. Mechanistically,...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833746/ https://www.ncbi.nlm.nih.gov/pubmed/29449541 http://dx.doi.org/10.1038/s41419-018-0305-7 |
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author | Zheng, Qidi Lin, Zhuojia Xu, Jie Lu, Yanan Meng, Qiuyu Wang, Chen Yang, Yuxin Xin, Xiaoru Li, Xiaonan Pu, Hu Gui, Xin Li, Tianming Xiong, Wujun Lu, Dongdong |
author_facet | Zheng, Qidi Lin, Zhuojia Xu, Jie Lu, Yanan Meng, Qiuyu Wang, Chen Yang, Yuxin Xin, Xiaoru Li, Xiaonan Pu, Hu Gui, Xin Li, Tianming Xiong, Wujun Lu, Dongdong |
author_sort | Zheng, Qidi |
collection | PubMed |
description | Maternally expressed gene 3 (MEG3) encodes an lncRNA which is suggested to function as a tumor suppressor and has been showed to involve in a variety of cancers. Herein, our findings demonstrate that MEG3 inhibits the malignant progression of liver cancer cells in vitro and in vivo. Mechanistically, MEG3 promotes the expression and maturition of miR122 which targets PKM2. Therefore, MEG3 decreases the expression and nuclear location of PKM2 dependent on miR122. Furthermore, MEG3 also inhibits CyclinD1 and C-Myc via PKM2 in liver cancer cells. On the other hand, MEG3 promotes β-catenin degradation through ubiquitin–proteasome system dependent on PTEN. Strikingly, MEG3 inhibits β-catenin activity through PKM2 reduction and PTEN increase. Significantly, we also found that excessive β-catenin abrogated the effect of MEG3 in liver cancer. In conclusion, our study for the first time demonstrates that MEG3 acts as a tumor suppressor by negatively regulating the activity of the PKM2 and β-catenin signaling pathway in hepatocarcinogenesis and could provide potential therapeutic targets for the treatment of liver cancer. |
format | Online Article Text |
id | pubmed-5833746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58337462018-03-06 Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN Zheng, Qidi Lin, Zhuojia Xu, Jie Lu, Yanan Meng, Qiuyu Wang, Chen Yang, Yuxin Xin, Xiaoru Li, Xiaonan Pu, Hu Gui, Xin Li, Tianming Xiong, Wujun Lu, Dongdong Cell Death Dis Article Maternally expressed gene 3 (MEG3) encodes an lncRNA which is suggested to function as a tumor suppressor and has been showed to involve in a variety of cancers. Herein, our findings demonstrate that MEG3 inhibits the malignant progression of liver cancer cells in vitro and in vivo. Mechanistically, MEG3 promotes the expression and maturition of miR122 which targets PKM2. Therefore, MEG3 decreases the expression and nuclear location of PKM2 dependent on miR122. Furthermore, MEG3 also inhibits CyclinD1 and C-Myc via PKM2 in liver cancer cells. On the other hand, MEG3 promotes β-catenin degradation through ubiquitin–proteasome system dependent on PTEN. Strikingly, MEG3 inhibits β-catenin activity through PKM2 reduction and PTEN increase. Significantly, we also found that excessive β-catenin abrogated the effect of MEG3 in liver cancer. In conclusion, our study for the first time demonstrates that MEG3 acts as a tumor suppressor by negatively regulating the activity of the PKM2 and β-catenin signaling pathway in hepatocarcinogenesis and could provide potential therapeutic targets for the treatment of liver cancer. Nature Publishing Group UK 2018-02-15 /pmc/articles/PMC5833746/ /pubmed/29449541 http://dx.doi.org/10.1038/s41419-018-0305-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zheng, Qidi Lin, Zhuojia Xu, Jie Lu, Yanan Meng, Qiuyu Wang, Chen Yang, Yuxin Xin, Xiaoru Li, Xiaonan Pu, Hu Gui, Xin Li, Tianming Xiong, Wujun Lu, Dongdong Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title | Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title_full | Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title_fullStr | Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title_full_unstemmed | Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title_short | Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN |
title_sort | long noncoding rna meg3 suppresses liver cancer cells growth through inhibiting β-catenin by activating pkm2 and inactivating pten |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833746/ https://www.ncbi.nlm.nih.gov/pubmed/29449541 http://dx.doi.org/10.1038/s41419-018-0305-7 |
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