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Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism

OBJECTIVE: The aim of this study is to discover the possible working mechanisms of Ardisiae Japonicae Herba (AJH) on hepatoma carcinoma (HCC). METHODS: In this study, ethanol extract of AJH was prepared and used to treat HCC cell in vitro. Furthermore, a genomic wide RNA sequencing (RNA-seq) was per...

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Autores principales: Gong, Xue, Cui, Huan-tian, Bian, Yu-hong, Li, Yu-ting, Wang, Yang-xue, Peng, Yan-fei, Wen, Wei-bo, Li, Kuan, Wang, Hong-wu, Zhang, Zhai-yi, Zheng, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476705/
https://www.ncbi.nlm.nih.gov/pubmed/36118924
http://dx.doi.org/10.1016/j.chmed.2021.06.003
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author Gong, Xue
Cui, Huan-tian
Bian, Yu-hong
Li, Yu-ting
Wang, Yang-xue
Peng, Yan-fei
Wen, Wei-bo
Li, Kuan
Wang, Hong-wu
Zhang, Zhai-yi
Zheng, Fang
author_facet Gong, Xue
Cui, Huan-tian
Bian, Yu-hong
Li, Yu-ting
Wang, Yang-xue
Peng, Yan-fei
Wen, Wei-bo
Li, Kuan
Wang, Hong-wu
Zhang, Zhai-yi
Zheng, Fang
author_sort Gong, Xue
collection PubMed
description OBJECTIVE: The aim of this study is to discover the possible working mechanisms of Ardisiae Japonicae Herba (AJH) on hepatoma carcinoma (HCC). METHODS: In this study, ethanol extract of AJH was prepared and used to treat HCC cell in vitro. Furthermore, a genomic wide RNA sequencing (RNA-seq) was performed to screen deregulated genes in HCC cells after the treatment of AJH extract. The gene and protein expression related to lipid metabolism in HCC cells were also investigated to validate the results obtained from RNA-seq. RESULTS: AJH extract could inhibit HCC cell proliferation in vitro. RNA-seq analysis has identified 1,601 differentially expressed genes (DEGs, fold change ≥ 2.0 or fold change ≤ 0.5, P < 0.05) in HCC after AJH extract treatment, which included 225 up-regulated genes and 1,376 down-regulated genes. KEGG pathway analysis of DEGs demonstrated that lipid metabolism was a potential pathway related to AJH treatment. In agreement with the RNA-seq data, qPCR and Western-blot analysis indicated that expression of genes and proteins related to lipid metabolism (SREBP1, ACC, ACLY and FASN) were significantly down-regulated in AJH treatment group as compared with the control group. Furthermore, AJH extract could also decrease lipid contents and cellular free fatty acid levels in HCC cells. CONCLUSION: Ethanol extract of AJH could inhibit HCC cell proliferation in vitro, the possible mechanism may be related to the inhibition of lipid metabolism.
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spelling pubmed-94767052022-09-16 Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism Gong, Xue Cui, Huan-tian Bian, Yu-hong Li, Yu-ting Wang, Yang-xue Peng, Yan-fei Wen, Wei-bo Li, Kuan Wang, Hong-wu Zhang, Zhai-yi Zheng, Fang Chin Herb Med Original Article OBJECTIVE: The aim of this study is to discover the possible working mechanisms of Ardisiae Japonicae Herba (AJH) on hepatoma carcinoma (HCC). METHODS: In this study, ethanol extract of AJH was prepared and used to treat HCC cell in vitro. Furthermore, a genomic wide RNA sequencing (RNA-seq) was performed to screen deregulated genes in HCC cells after the treatment of AJH extract. The gene and protein expression related to lipid metabolism in HCC cells were also investigated to validate the results obtained from RNA-seq. RESULTS: AJH extract could inhibit HCC cell proliferation in vitro. RNA-seq analysis has identified 1,601 differentially expressed genes (DEGs, fold change ≥ 2.0 or fold change ≤ 0.5, P < 0.05) in HCC after AJH extract treatment, which included 225 up-regulated genes and 1,376 down-regulated genes. KEGG pathway analysis of DEGs demonstrated that lipid metabolism was a potential pathway related to AJH treatment. In agreement with the RNA-seq data, qPCR and Western-blot analysis indicated that expression of genes and proteins related to lipid metabolism (SREBP1, ACC, ACLY and FASN) were significantly down-regulated in AJH treatment group as compared with the control group. Furthermore, AJH extract could also decrease lipid contents and cellular free fatty acid levels in HCC cells. CONCLUSION: Ethanol extract of AJH could inhibit HCC cell proliferation in vitro, the possible mechanism may be related to the inhibition of lipid metabolism. Elsevier 2021-06-28 /pmc/articles/PMC9476705/ /pubmed/36118924 http://dx.doi.org/10.1016/j.chmed.2021.06.003 Text en © 2021 Tianjin Press of Chinese Herbal Medicines. Published by ELSEVIER B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Gong, Xue
Cui, Huan-tian
Bian, Yu-hong
Li, Yu-ting
Wang, Yang-xue
Peng, Yan-fei
Wen, Wei-bo
Li, Kuan
Wang, Hong-wu
Zhang, Zhai-yi
Zheng, Fang
Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title_full Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title_fullStr Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title_full_unstemmed Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title_short Ethanol extract of Ardisiae Japonicae Herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
title_sort ethanol extract of ardisiae japonicae herba inhibits hepatoma carcinoma cell proliferation in vitro through regulating lipid metabolism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476705/
https://www.ncbi.nlm.nih.gov/pubmed/36118924
http://dx.doi.org/10.1016/j.chmed.2021.06.003
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