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JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells

BACKGROUND: Studies have shown that Jianpi Huayu Decoction (JPHYD) can inhibit the growth of hepatocellular carcinoma cells, but the mechanism of its effect was not clear at present. METHODS: We assessed the effect of JPHYD using liver cancer cells as in vitro cell model and xenograft tumor as in vi...

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Autores principales: Liu, Li-Hua, Fang, Chong-Kai, Ge, Fu-Cheng, Wang, Ji-Nan, Zhang, Xiu-Bing, Luo, Rui, Zhang, Ying, Feng, Kun-Liang, Qiu, Zhen-Wen, Zhong, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064503/
https://www.ncbi.nlm.nih.gov/pubmed/35518787
http://dx.doi.org/10.1155/2022/7823433
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author Liu, Li-Hua
Fang, Chong-Kai
Ge, Fu-Cheng
Wang, Ji-Nan
Zhang, Xiu-Bing
Luo, Rui
Zhang, Ying
Feng, Kun-Liang
Qiu, Zhen-Wen
Zhong, Chong
author_facet Liu, Li-Hua
Fang, Chong-Kai
Ge, Fu-Cheng
Wang, Ji-Nan
Zhang, Xiu-Bing
Luo, Rui
Zhang, Ying
Feng, Kun-Liang
Qiu, Zhen-Wen
Zhong, Chong
author_sort Liu, Li-Hua
collection PubMed
description BACKGROUND: Studies have shown that Jianpi Huayu Decoction (JPHYD) can inhibit the growth of hepatocellular carcinoma cells, but the mechanism of its effect was not clear at present. METHODS: We assessed the effect of JPHYD using liver cancer cells as in vitro cell model and xenograft tumor as in vivo model. CCK8, EdU, wound-healing, and transwell assays were performed to assess the cell growth, migration, and invasion of hepatocellular carcinoma (HCC) cell lines HepG2 and MHCC97H. Western blot assay was performed to observe the protein level of E-cadherin, Smad7, N-cadherin, Snail, Smad3, Vimentin, and Zeb1. qRT-PCR assay was used to observe the expression of miR-21-5p in clinical liver cancer tissue samples and in HepG2 and MHCC97H cells. Animal tumorigenesis experiments and in vivo imaging experiments were performed to assess the results of in vitro experiments. RESULTS: We found that JPHYD could inhibit the proliferation, invasion, and migration of hepatocellular carcinoma cells and JPHYD decreased the level of N-cadherin, Snail, Vimentin, Smad3, and Zeb1 and increased E-cadherin and Smad7 proteins. The expression of miR-21-5p was increased while that protein of Smad7 was decreased in HCC tissues. The vivo experiments also showed that miR-21-5p could promote the migration of HCC cells. JPHYD decreased miR-21-5p expression. The same results have been found in animal studies. CONCLUSION: Our results indicated that JPHYD inhibited epithelial-mesenchymal transition by increasing Smad7 expression and inhibiting miR-21-5p. Therefore, blocking the occurrence and development of EMT may be a new mechanism of JPHYD's anti-liver cancer effect.
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spelling pubmed-90645032022-05-04 JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells Liu, Li-Hua Fang, Chong-Kai Ge, Fu-Cheng Wang, Ji-Nan Zhang, Xiu-Bing Luo, Rui Zhang, Ying Feng, Kun-Liang Qiu, Zhen-Wen Zhong, Chong J Oncol Research Article BACKGROUND: Studies have shown that Jianpi Huayu Decoction (JPHYD) can inhibit the growth of hepatocellular carcinoma cells, but the mechanism of its effect was not clear at present. METHODS: We assessed the effect of JPHYD using liver cancer cells as in vitro cell model and xenograft tumor as in vivo model. CCK8, EdU, wound-healing, and transwell assays were performed to assess the cell growth, migration, and invasion of hepatocellular carcinoma (HCC) cell lines HepG2 and MHCC97H. Western blot assay was performed to observe the protein level of E-cadherin, Smad7, N-cadherin, Snail, Smad3, Vimentin, and Zeb1. qRT-PCR assay was used to observe the expression of miR-21-5p in clinical liver cancer tissue samples and in HepG2 and MHCC97H cells. Animal tumorigenesis experiments and in vivo imaging experiments were performed to assess the results of in vitro experiments. RESULTS: We found that JPHYD could inhibit the proliferation, invasion, and migration of hepatocellular carcinoma cells and JPHYD decreased the level of N-cadherin, Snail, Vimentin, Smad3, and Zeb1 and increased E-cadherin and Smad7 proteins. The expression of miR-21-5p was increased while that protein of Smad7 was decreased in HCC tissues. The vivo experiments also showed that miR-21-5p could promote the migration of HCC cells. JPHYD decreased miR-21-5p expression. The same results have been found in animal studies. CONCLUSION: Our results indicated that JPHYD inhibited epithelial-mesenchymal transition by increasing Smad7 expression and inhibiting miR-21-5p. Therefore, blocking the occurrence and development of EMT may be a new mechanism of JPHYD's anti-liver cancer effect. Hindawi 2022-04-26 /pmc/articles/PMC9064503/ /pubmed/35518787 http://dx.doi.org/10.1155/2022/7823433 Text en Copyright © 2022 Li-Hua Liu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Li-Hua
Fang, Chong-Kai
Ge, Fu-Cheng
Wang, Ji-Nan
Zhang, Xiu-Bing
Luo, Rui
Zhang, Ying
Feng, Kun-Liang
Qiu, Zhen-Wen
Zhong, Chong
JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title_full JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title_fullStr JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title_full_unstemmed JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title_short JPHYD Inhibits miR-21-5p/Smad7-Mediated Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells
title_sort jphyd inhibits mir-21-5p/smad7-mediated epithelial-mesenchymal transition of hepatocellular carcinoma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064503/
https://www.ncbi.nlm.nih.gov/pubmed/35518787
http://dx.doi.org/10.1155/2022/7823433
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