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Potential of antiviral drug oseltamivir for the treatment of liver cancer

Liver cancer is a leading cause of cancer-related mortality globally. Since hepatitis virus infections have been strongly associated with the incidence of liver cancer, studies concerning the effects of antiviral drugs on liver cancer have attracted great attention in recent years. The present study...

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Autores principales: Huang, Pei-Ju, Chiu, Chun-Ching, Hsiao, Min-Hua, Le Yow, Jia, Tzang, Bor-Show, Hsu, Tsai-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651232/
https://www.ncbi.nlm.nih.gov/pubmed/34859259
http://dx.doi.org/10.3892/ijo.2021.5289
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author Huang, Pei-Ju
Chiu, Chun-Ching
Hsiao, Min-Hua
Le Yow, Jia
Tzang, Bor-Show
Hsu, Tsai-Ching
author_facet Huang, Pei-Ju
Chiu, Chun-Ching
Hsiao, Min-Hua
Le Yow, Jia
Tzang, Bor-Show
Hsu, Tsai-Ching
author_sort Huang, Pei-Ju
collection PubMed
description Liver cancer is a leading cause of cancer-related mortality globally. Since hepatitis virus infections have been strongly associated with the incidence of liver cancer, studies concerning the effects of antiviral drugs on liver cancer have attracted great attention in recent years. The present study investigated the effects of two anti-hepatitis virus drugs, lamivudine and ribavirin, and one anti-influenza virus drug, oseltamivir, on liver cancer cells to assess alternative methods for treating liver cancer. MTT assays, wound healing assays, Transwell assays, flow cytometry, immunoblotting, ELISA, immunofluorescence staining and a xenograft animal model were adopted to verify the effects of lamivudine, ribavirin and oseltamivir on liver cancer cells. Treatment with ribavirin and oseltamivir for 24 and 48 h significantly decreased the viability of both Huh-7 and HepG2 cells compared with that of THLE-3 cells in a dose-dependent manner. The subsequent investigations focused on oseltamivir, considering the more serious clinical adverse effects of ribavirin than those of oseltamivir. Significantly decreased migration and invasion were observed in both Huh-7 and HepG2 cells that were treated with oseltamivir for 24 and 48 h. In addition, oseltamivir significantly increased autophagy in Huh-7 cells, as revealed by the significantly higher ratios of LC3-II/LC3-I, increased expression of Beclin-1, and decreased expression of p62, whereas no significant increases in the expression of apoptosis-related proteins, including Apaf-1, cleaved caspase-3, and cleaved PARP-1, were detected. Notably, apoptosis and autophagy were significantly increased in HepG2 cells in the presence of oseltamivir, as revealed by the significant increases in the expression of Apaf-1, cleaved caspase-3, and cleaved PARP-1, the higher ratios of LC3-II/LC3-I, the increased expression of Beclin-1, and the decreased expression of p62. Additionally, significant inhibitory effects of oseltamivir on xenografted Huh-7 cells in athymic nude mice were observed. The present study, for the first time to the best of our knowledge, reported the differential effects of oseltamivir on inducing liver cancer cell death both in vitro and in vivo and may provide an alternative approach for treating liver cancer.
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spelling pubmed-86512322021-12-20 Potential of antiviral drug oseltamivir for the treatment of liver cancer Huang, Pei-Ju Chiu, Chun-Ching Hsiao, Min-Hua Le Yow, Jia Tzang, Bor-Show Hsu, Tsai-Ching Int J Oncol Articles Liver cancer is a leading cause of cancer-related mortality globally. Since hepatitis virus infections have been strongly associated with the incidence of liver cancer, studies concerning the effects of antiviral drugs on liver cancer have attracted great attention in recent years. The present study investigated the effects of two anti-hepatitis virus drugs, lamivudine and ribavirin, and one anti-influenza virus drug, oseltamivir, on liver cancer cells to assess alternative methods for treating liver cancer. MTT assays, wound healing assays, Transwell assays, flow cytometry, immunoblotting, ELISA, immunofluorescence staining and a xenograft animal model were adopted to verify the effects of lamivudine, ribavirin and oseltamivir on liver cancer cells. Treatment with ribavirin and oseltamivir for 24 and 48 h significantly decreased the viability of both Huh-7 and HepG2 cells compared with that of THLE-3 cells in a dose-dependent manner. The subsequent investigations focused on oseltamivir, considering the more serious clinical adverse effects of ribavirin than those of oseltamivir. Significantly decreased migration and invasion were observed in both Huh-7 and HepG2 cells that were treated with oseltamivir for 24 and 48 h. In addition, oseltamivir significantly increased autophagy in Huh-7 cells, as revealed by the significantly higher ratios of LC3-II/LC3-I, increased expression of Beclin-1, and decreased expression of p62, whereas no significant increases in the expression of apoptosis-related proteins, including Apaf-1, cleaved caspase-3, and cleaved PARP-1, were detected. Notably, apoptosis and autophagy were significantly increased in HepG2 cells in the presence of oseltamivir, as revealed by the significant increases in the expression of Apaf-1, cleaved caspase-3, and cleaved PARP-1, the higher ratios of LC3-II/LC3-I, the increased expression of Beclin-1, and the decreased expression of p62. Additionally, significant inhibitory effects of oseltamivir on xenografted Huh-7 cells in athymic nude mice were observed. The present study, for the first time to the best of our knowledge, reported the differential effects of oseltamivir on inducing liver cancer cell death both in vitro and in vivo and may provide an alternative approach for treating liver cancer. D.A. Spandidos 2021-12-02 /pmc/articles/PMC8651232/ /pubmed/34859259 http://dx.doi.org/10.3892/ijo.2021.5289 Text en Copyright: © Huang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Huang, Pei-Ju
Chiu, Chun-Ching
Hsiao, Min-Hua
Le Yow, Jia
Tzang, Bor-Show
Hsu, Tsai-Ching
Potential of antiviral drug oseltamivir for the treatment of liver cancer
title Potential of antiviral drug oseltamivir for the treatment of liver cancer
title_full Potential of antiviral drug oseltamivir for the treatment of liver cancer
title_fullStr Potential of antiviral drug oseltamivir for the treatment of liver cancer
title_full_unstemmed Potential of antiviral drug oseltamivir for the treatment of liver cancer
title_short Potential of antiviral drug oseltamivir for the treatment of liver cancer
title_sort potential of antiviral drug oseltamivir for the treatment of liver cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651232/
https://www.ncbi.nlm.nih.gov/pubmed/34859259
http://dx.doi.org/10.3892/ijo.2021.5289
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