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A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT
Liver cancer, also known as primary liver cancer, is cancer that starts in the liver. JNU-144, a new meroterpenoid purified from Lithospermum erythrorhizon, has exhibited promising anticancer activity; however, the molecular mechanisms of action of JNU-144 on malignant cells remain unclear. Our stud...
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/PMC6120861/ https://www.ncbi.nlm.nih.gov/pubmed/30177727 http://dx.doi.org/10.1038/s41598-018-31409-2 |
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author | Wan, Haoqiang Li, Jiemei Zhang, Keda Zou, Xiaoting Ge, Lanlan Zhu, Fuqiang Zhou, Huirong Gong, Minna Wang, Tianwa Chen, Dongling Peng, Shusong Zhou, Boping Zeng, Xiaobin |
author_facet | Wan, Haoqiang Li, Jiemei Zhang, Keda Zou, Xiaoting Ge, Lanlan Zhu, Fuqiang Zhou, Huirong Gong, Minna Wang, Tianwa Chen, Dongling Peng, Shusong Zhou, Boping Zeng, Xiaobin |
author_sort | Wan, Haoqiang |
collection | PubMed |
description | Liver cancer, also known as primary liver cancer, is cancer that starts in the liver. JNU-144, a new meroterpenoid purified from Lithospermum erythrorhizon, has exhibited promising anticancer activity; however, the molecular mechanisms of action of JNU-144 on malignant cells remain unclear. Our studies revealed that JNU-144 suppressed cell viability and proliferation in hepatoma cells by downregulating mTOR activation. Meanwhile, JNU-144 activated the intrinsic apoptosis pathway and subsequently triggered apoptotic cell death in SMMC-7721 cells. We also found that JNU-144 inhibited the epithelial–mesenchymal transition in both SMMC-7721 and HepG2 cells through reprogramming of epithelial–mesenchymal transition (EMT)-related gene expression or regulating protein instability. These findings indicate that JNU-144 exerts potent anticancer activity in hepatoma cells and may be developed as a potential therapeutic drug. |
format | Online Article Text |
id | pubmed-6120861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61208612018-09-06 A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT Wan, Haoqiang Li, Jiemei Zhang, Keda Zou, Xiaoting Ge, Lanlan Zhu, Fuqiang Zhou, Huirong Gong, Minna Wang, Tianwa Chen, Dongling Peng, Shusong Zhou, Boping Zeng, Xiaobin Sci Rep Article Liver cancer, also known as primary liver cancer, is cancer that starts in the liver. JNU-144, a new meroterpenoid purified from Lithospermum erythrorhizon, has exhibited promising anticancer activity; however, the molecular mechanisms of action of JNU-144 on malignant cells remain unclear. Our studies revealed that JNU-144 suppressed cell viability and proliferation in hepatoma cells by downregulating mTOR activation. Meanwhile, JNU-144 activated the intrinsic apoptosis pathway and subsequently triggered apoptotic cell death in SMMC-7721 cells. We also found that JNU-144 inhibited the epithelial–mesenchymal transition in both SMMC-7721 and HepG2 cells through reprogramming of epithelial–mesenchymal transition (EMT)-related gene expression or regulating protein instability. These findings indicate that JNU-144 exerts potent anticancer activity in hepatoma cells and may be developed as a potential therapeutic drug. Nature Publishing Group UK 2018-09-03 /pmc/articles/PMC6120861/ /pubmed/30177727 http://dx.doi.org/10.1038/s41598-018-31409-2 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 Wan, Haoqiang Li, Jiemei Zhang, Keda Zou, Xiaoting Ge, Lanlan Zhu, Fuqiang Zhou, Huirong Gong, Minna Wang, Tianwa Chen, Dongling Peng, Shusong Zhou, Boping Zeng, Xiaobin A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title | A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title_full | A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title_fullStr | A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title_full_unstemmed | A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title_short | A new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mTOR activation and inhibiting EMT |
title_sort | new meroterpenoid functions as an anti-tumor agent in hepatoma cells by downregulating mtor activation and inhibiting emt |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120861/ https://www.ncbi.nlm.nih.gov/pubmed/30177727 http://dx.doi.org/10.1038/s41598-018-31409-2 |
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