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Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma
Tissue factor (TF) is a transmembrane glycoprotein to initiate blood coagulation and frequently overexpressed in a variety of tumors. Our previous study has showed that the expression of TF is upregulated and correlated with prognosis in hepatocellular carcinoma (HCC). However, the role and molecula...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428933/ https://www.ncbi.nlm.nih.gov/pubmed/30931258 http://dx.doi.org/10.3389/fonc.2019.00150 |
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author | Huang, Shan-Zhou Wei, Meng-Ning Huang, Jia-Rong Zhang, Zi-Jian Zhang, Wen-Ji Jiang, Qi-Wei Yang, Yang Wang, Huan-Yu Jin, Hui-Lin Wang, Kun Xing, Zi-Hao Yuan, Meng-Ling Li, Yao He, Xiao-Shun Shi, Zhi Zhou, Qi |
author_facet | Huang, Shan-Zhou Wei, Meng-Ning Huang, Jia-Rong Zhang, Zi-Jian Zhang, Wen-Ji Jiang, Qi-Wei Yang, Yang Wang, Huan-Yu Jin, Hui-Lin Wang, Kun Xing, Zi-Hao Yuan, Meng-Ling Li, Yao He, Xiao-Shun Shi, Zhi Zhou, Qi |
author_sort | Huang, Shan-Zhou |
collection | PubMed |
description | Tissue factor (TF) is a transmembrane glycoprotein to initiate blood coagulation and frequently overexpressed in a variety of tumors. Our previous study has showed that the expression of TF is upregulated and correlated with prognosis in hepatocellular carcinoma (HCC). However, the role and molecular mechanism of TF in the growth of HCC are still unclear. In vitro and in vivo functional experiments were performed to determine the effect of TF on the growth of HCC cells. A panel of biochemical assays was used to elucidate the underlying mechanisms. TF could promote the growth of HCC in vitro and in vivo by activating both ERK and AKT signaling pathways. TF induced EGFR upregualtion, and inhibition of EGFR suppressed TF-mediated HCC growth. In addition, TF protein expression was correlated with EGFR in HCC tissues. TF promotes HCC growth by upregulation of EGFR, and TF as well as EGFR may be potential therapeutic targets of HCC. |
format | Online Article Text |
id | pubmed-6428933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64289332019-03-29 Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma Huang, Shan-Zhou Wei, Meng-Ning Huang, Jia-Rong Zhang, Zi-Jian Zhang, Wen-Ji Jiang, Qi-Wei Yang, Yang Wang, Huan-Yu Jin, Hui-Lin Wang, Kun Xing, Zi-Hao Yuan, Meng-Ling Li, Yao He, Xiao-Shun Shi, Zhi Zhou, Qi Front Oncol Oncology Tissue factor (TF) is a transmembrane glycoprotein to initiate blood coagulation and frequently overexpressed in a variety of tumors. Our previous study has showed that the expression of TF is upregulated and correlated with prognosis in hepatocellular carcinoma (HCC). However, the role and molecular mechanism of TF in the growth of HCC are still unclear. In vitro and in vivo functional experiments were performed to determine the effect of TF on the growth of HCC cells. A panel of biochemical assays was used to elucidate the underlying mechanisms. TF could promote the growth of HCC in vitro and in vivo by activating both ERK and AKT signaling pathways. TF induced EGFR upregualtion, and inhibition of EGFR suppressed TF-mediated HCC growth. In addition, TF protein expression was correlated with EGFR in HCC tissues. TF promotes HCC growth by upregulation of EGFR, and TF as well as EGFR may be potential therapeutic targets of HCC. Frontiers Media S.A. 2019-03-15 /pmc/articles/PMC6428933/ /pubmed/30931258 http://dx.doi.org/10.3389/fonc.2019.00150 Text en Copyright © 2019 Huang, Wei, Huang, Zhang, Zhang, Jiang, Yang, Wang, Jin, Wang, Xing, Yuan, Li, He, Shi and Zhou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Huang, Shan-Zhou Wei, Meng-Ning Huang, Jia-Rong Zhang, Zi-Jian Zhang, Wen-Ji Jiang, Qi-Wei Yang, Yang Wang, Huan-Yu Jin, Hui-Lin Wang, Kun Xing, Zi-Hao Yuan, Meng-Ling Li, Yao He, Xiao-Shun Shi, Zhi Zhou, Qi Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title | Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title_full | Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title_fullStr | Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title_full_unstemmed | Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title_short | Targeting TF-AKT/ERK-EGFR Pathway Suppresses the Growth of Hepatocellular Carcinoma |
title_sort | targeting tf-akt/erk-egfr pathway suppresses the growth of hepatocellular carcinoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428933/ https://www.ncbi.nlm.nih.gov/pubmed/30931258 http://dx.doi.org/10.3389/fonc.2019.00150 |
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