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Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation
Dexmedetomidine (DEX) is an anesthetic that is widely used in the clinic, and it has been reported to exhibit paradoxical effects in the progression of multiple solid tumors. In this study, we sought to explore the mechanism by which DEX regulates hepatocellular carcinoma (HCC) progression underlyin...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080602/ https://www.ncbi.nlm.nih.gov/pubmed/32632241 http://dx.doi.org/10.1038/s12276-020-0461-6 |
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author | Chen, Peng Luo, Xiaojun Dai, Guanqi Jiang, Yuchuan Luo, Yue Peng, Shuang Wang, Hao Xie, Penghui Qu, Chen Lin, Wenyu Hong, Jian Ning, Xue Li, Aimin |
author_facet | Chen, Peng Luo, Xiaojun Dai, Guanqi Jiang, Yuchuan Luo, Yue Peng, Shuang Wang, Hao Xie, Penghui Qu, Chen Lin, Wenyu Hong, Jian Ning, Xue Li, Aimin |
author_sort | Chen, Peng |
collection | PubMed |
description | Dexmedetomidine (DEX) is an anesthetic that is widely used in the clinic, and it has been reported to exhibit paradoxical effects in the progression of multiple solid tumors. In this study, we sought to explore the mechanism by which DEX regulates hepatocellular carcinoma (HCC) progression underlying liver fibrosis. We determined the effects of DEX on tumor progression in an orthotopic HCC mouse model of fibrotic liver. A coculture system and a subcutaneous xenograft model involving coimplantation of mouse hepatoma cells (H22) and primary activated hepatic stellate cells (aHSCs) were used to study the effects of DEX on HCC progression. We found that in the preclinical mouse model of liver fibrosis, DEX treatment significantly shortened median survival time and promoted tumor growth, intrahepatic metastasis and pulmonary metastasis. The DEX receptor (ADRA2A) was mainly expressed in aHSCs but was barely detected in HCC cells. DEX dramatically reinforced HCC malignant behaviors in the presence of aHSCs in both the coculture system and the coimplantation mouse model, but DEX alone exerted no significant effects on the malignancy of HCC. Mechanistically, DEX induced IL-6 secretion from aHSCs and promoted HCC progression via STAT3 activation. Our findings provide evidence that the clinical application of DEX may cause undesirable side effects in HCC patients with liver fibrosis. |
format | Online Article Text |
id | pubmed-8080602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80806022021-04-29 Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation Chen, Peng Luo, Xiaojun Dai, Guanqi Jiang, Yuchuan Luo, Yue Peng, Shuang Wang, Hao Xie, Penghui Qu, Chen Lin, Wenyu Hong, Jian Ning, Xue Li, Aimin Exp Mol Med Article Dexmedetomidine (DEX) is an anesthetic that is widely used in the clinic, and it has been reported to exhibit paradoxical effects in the progression of multiple solid tumors. In this study, we sought to explore the mechanism by which DEX regulates hepatocellular carcinoma (HCC) progression underlying liver fibrosis. We determined the effects of DEX on tumor progression in an orthotopic HCC mouse model of fibrotic liver. A coculture system and a subcutaneous xenograft model involving coimplantation of mouse hepatoma cells (H22) and primary activated hepatic stellate cells (aHSCs) were used to study the effects of DEX on HCC progression. We found that in the preclinical mouse model of liver fibrosis, DEX treatment significantly shortened median survival time and promoted tumor growth, intrahepatic metastasis and pulmonary metastasis. The DEX receptor (ADRA2A) was mainly expressed in aHSCs but was barely detected in HCC cells. DEX dramatically reinforced HCC malignant behaviors in the presence of aHSCs in both the coculture system and the coimplantation mouse model, but DEX alone exerted no significant effects on the malignancy of HCC. Mechanistically, DEX induced IL-6 secretion from aHSCs and promoted HCC progression via STAT3 activation. Our findings provide evidence that the clinical application of DEX may cause undesirable side effects in HCC patients with liver fibrosis. Nature Publishing Group UK 2020-07-06 /pmc/articles/PMC8080602/ /pubmed/32632241 http://dx.doi.org/10.1038/s12276-020-0461-6 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chen, Peng Luo, Xiaojun Dai, Guanqi Jiang, Yuchuan Luo, Yue Peng, Shuang Wang, Hao Xie, Penghui Qu, Chen Lin, Wenyu Hong, Jian Ning, Xue Li, Aimin Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title | Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title_full | Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title_fullStr | Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title_full_unstemmed | Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title_short | Dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
title_sort | dexmedetomidine promotes the progression of hepatocellular carcinoma through hepatic stellate cell activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080602/ https://www.ncbi.nlm.nih.gov/pubmed/32632241 http://dx.doi.org/10.1038/s12276-020-0461-6 |
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