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Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins

PURPOSE: Hepatocellular carcinoma (HCC) is a common malignant tumor with limited treatment. Our previous studies demonstrated that Huaier enhanced chemotherapy sensitivity and restrained HCC proliferation. This study aimed to identify differentially expressed proteins with Huaier treatment in HCC ce...

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Autores principales: Niu, Yongjie, Shan, Liang, Gao, Han, Zhang, Congcong, Qian, Zijun, Wang, Zhixian, Xu, Xin, Zhang, Xiao, Wang, Jiayi, Ma, Lifang, Chen, Liyun, Yu, Yongchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685376/
https://www.ncbi.nlm.nih.gov/pubmed/33244243
http://dx.doi.org/10.2147/OTT.S279723
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author Niu, Yongjie
Shan, Liang
Gao, Han
Zhang, Congcong
Qian, Zijun
Wang, Zhixian
Xu, Xin
Zhang, Xiao
Wang, Jiayi
Ma, Lifang
Chen, Liyun
Yu, Yongchun
author_facet Niu, Yongjie
Shan, Liang
Gao, Han
Zhang, Congcong
Qian, Zijun
Wang, Zhixian
Xu, Xin
Zhang, Xiao
Wang, Jiayi
Ma, Lifang
Chen, Liyun
Yu, Yongchun
author_sort Niu, Yongjie
collection PubMed
description PURPOSE: Hepatocellular carcinoma (HCC) is a common malignant tumor with limited treatment. Our previous studies demonstrated that Huaier enhanced chemotherapy sensitivity and restrained HCC proliferation. This study aimed to identify differentially expressed proteins with Huaier treatment in HCC cells, providing molecular targets for future targeted therapy of HCC. MATERIALS AND METHODS: The effects of Huaier on the cell cycle were determined by flow cytometry and Western blot (WB). Xenograft models were used to verify the effects of Huaier on tumor growth. Then, proteomics was performed to identify the potential proteins regulated by Huaier. The enrichment analysis of GO and KEGG was performed for the differentially expressed proteins. Western blot (WB) and immunohistochemistry (IHC) were used to detect the levels of proteins after Huaier treatment. After that the correlation of differentially expressed proteins with pathological stages was analyzed via the GEPIA database. We also analyzed candidate expression after Huaier treatment in HCC cells by WB and qRT-PCR. Furthermore, siRNA was performed to verify the targeted regulation of Huaier on candidate proteins. RESULTS: First, the proteomics data showed that a total of 160 proteins were identified as differentially expressed proteins, among which six minichromosome maintenance (MCM) family members were enriched in the tumor-associated pathways after Huaier treatment. Moreover, MCM proteins were highly expressed in HCC and closely correlated with the survival of HCC patients. Finally, we confirmed that MCM proteins were targets of Huaier treatment in HCC cells. CONCLUSION: Huaier treatment was closely associated with the activation and inhibition of cancer-related pathways, and the MCM family was identified as a potential target in the antitumor process of Huaier. This study is helpful in understanding the molecular alterations and clinical relevance of HCC after Huaier treatment, which is beneficial for finding new targets and designing effective chemotherapy regimens for the future treatment of HCC.
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spelling pubmed-76853762020-11-25 Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins Niu, Yongjie Shan, Liang Gao, Han Zhang, Congcong Qian, Zijun Wang, Zhixian Xu, Xin Zhang, Xiao Wang, Jiayi Ma, Lifang Chen, Liyun Yu, Yongchun Onco Targets Ther Original Research PURPOSE: Hepatocellular carcinoma (HCC) is a common malignant tumor with limited treatment. Our previous studies demonstrated that Huaier enhanced chemotherapy sensitivity and restrained HCC proliferation. This study aimed to identify differentially expressed proteins with Huaier treatment in HCC cells, providing molecular targets for future targeted therapy of HCC. MATERIALS AND METHODS: The effects of Huaier on the cell cycle were determined by flow cytometry and Western blot (WB). Xenograft models were used to verify the effects of Huaier on tumor growth. Then, proteomics was performed to identify the potential proteins regulated by Huaier. The enrichment analysis of GO and KEGG was performed for the differentially expressed proteins. Western blot (WB) and immunohistochemistry (IHC) were used to detect the levels of proteins after Huaier treatment. After that the correlation of differentially expressed proteins with pathological stages was analyzed via the GEPIA database. We also analyzed candidate expression after Huaier treatment in HCC cells by WB and qRT-PCR. Furthermore, siRNA was performed to verify the targeted regulation of Huaier on candidate proteins. RESULTS: First, the proteomics data showed that a total of 160 proteins were identified as differentially expressed proteins, among which six minichromosome maintenance (MCM) family members were enriched in the tumor-associated pathways after Huaier treatment. Moreover, MCM proteins were highly expressed in HCC and closely correlated with the survival of HCC patients. Finally, we confirmed that MCM proteins were targets of Huaier treatment in HCC cells. CONCLUSION: Huaier treatment was closely associated with the activation and inhibition of cancer-related pathways, and the MCM family was identified as a potential target in the antitumor process of Huaier. This study is helpful in understanding the molecular alterations and clinical relevance of HCC after Huaier treatment, which is beneficial for finding new targets and designing effective chemotherapy regimens for the future treatment of HCC. Dove 2020-11-20 /pmc/articles/PMC7685376/ /pubmed/33244243 http://dx.doi.org/10.2147/OTT.S279723 Text en © 2020 Niu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Niu, Yongjie
Shan, Liang
Gao, Han
Zhang, Congcong
Qian, Zijun
Wang, Zhixian
Xu, Xin
Zhang, Xiao
Wang, Jiayi
Ma, Lifang
Chen, Liyun
Yu, Yongchun
Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title_full Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title_fullStr Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title_full_unstemmed Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title_short Huaier Suppresses the Hepatocellular Carcinoma Cell Cycle by Regulating Minichromosome Maintenance Proteins
title_sort huaier suppresses the hepatocellular carcinoma cell cycle by regulating minichromosome maintenance proteins
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685376/
https://www.ncbi.nlm.nih.gov/pubmed/33244243
http://dx.doi.org/10.2147/OTT.S279723
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