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Karonudib is a promising anticancer therapy in hepatocellular carcinoma
BACKGROUND: Hepatocellular carcinoma (HCC) is the most common form of liver cancer and is generally caused by viral infections or consumption of mutagens, such as alcohol. While liver transplantation and hepatectomy is curative for some patients, many relapse into disease with few treatment options...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710815/ https://www.ncbi.nlm.nih.gov/pubmed/31489034 http://dx.doi.org/10.1177/1758835919866960 |
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author | Hua, Xiangwei Sanjiv, Kumar Gad, Helge Pham, Therese Gokturk, Camilla Rasti, Azita Zhao, Zhenjun He, Kang Feng, Mingxuan Zang, Yunjin Zhang, Jianjun Xia, Qiang Helleday, Thomas Warpman Berglund, Ulrika |
author_facet | Hua, Xiangwei Sanjiv, Kumar Gad, Helge Pham, Therese Gokturk, Camilla Rasti, Azita Zhao, Zhenjun He, Kang Feng, Mingxuan Zang, Yunjin Zhang, Jianjun Xia, Qiang Helleday, Thomas Warpman Berglund, Ulrika |
author_sort | Hua, Xiangwei |
collection | PubMed |
description | BACKGROUND: Hepatocellular carcinoma (HCC) is the most common form of liver cancer and is generally caused by viral infections or consumption of mutagens, such as alcohol. While liver transplantation and hepatectomy is curative for some patients, many relapse into disease with few treatment options such as tyrosine kinase inhibitors, for example, sorafenib or lenvatinib. The need for novel systemic treatment approaches is urgent. METHODS: MTH1 expression profile was first analyzed in a HCC database and MTH1 mRNA/protein level was determined in resected HCC and paired paracancerous tissues with polymerase chain reaction (PCR) and immunohistochemistry. HCC cancer cell lines were exposed in vitro to MTH1 inhibitors or depleted of MTH1 by siRNA. 8-oxoG was measured by the modified comet assay. The effect of MTH1 inhibition on tumor growth was explored in HCC xenograft in vivo models. RESULTS: MTH1 protein level is elevated in HCC tissue compared with paracancerous liver tissue and indicates poor prognosis. The MTH1 inhibitor Karonudib (TH1579) and siRNA effectively introduce toxic oxidized nucleotides into DNA, 8-oxoG, and kill HCC cell lines in vitro. Furthermore, we demonstrate that HCC growth in a xenograft mouse model in vivo is efficiently suppressed by Karonudib. CONCLUSION: Altogether, these data suggest HCC relies on MTH1 for survival, which can be targeted and may open up a novel treatment option for HCC in the future. |
format | Online Article Text |
id | pubmed-6710815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67108152019-09-05 Karonudib is a promising anticancer therapy in hepatocellular carcinoma Hua, Xiangwei Sanjiv, Kumar Gad, Helge Pham, Therese Gokturk, Camilla Rasti, Azita Zhao, Zhenjun He, Kang Feng, Mingxuan Zang, Yunjin Zhang, Jianjun Xia, Qiang Helleday, Thomas Warpman Berglund, Ulrika Ther Adv Med Oncol Original Research BACKGROUND: Hepatocellular carcinoma (HCC) is the most common form of liver cancer and is generally caused by viral infections or consumption of mutagens, such as alcohol. While liver transplantation and hepatectomy is curative for some patients, many relapse into disease with few treatment options such as tyrosine kinase inhibitors, for example, sorafenib or lenvatinib. The need for novel systemic treatment approaches is urgent. METHODS: MTH1 expression profile was first analyzed in a HCC database and MTH1 mRNA/protein level was determined in resected HCC and paired paracancerous tissues with polymerase chain reaction (PCR) and immunohistochemistry. HCC cancer cell lines were exposed in vitro to MTH1 inhibitors or depleted of MTH1 by siRNA. 8-oxoG was measured by the modified comet assay. The effect of MTH1 inhibition on tumor growth was explored in HCC xenograft in vivo models. RESULTS: MTH1 protein level is elevated in HCC tissue compared with paracancerous liver tissue and indicates poor prognosis. The MTH1 inhibitor Karonudib (TH1579) and siRNA effectively introduce toxic oxidized nucleotides into DNA, 8-oxoG, and kill HCC cell lines in vitro. Furthermore, we demonstrate that HCC growth in a xenograft mouse model in vivo is efficiently suppressed by Karonudib. CONCLUSION: Altogether, these data suggest HCC relies on MTH1 for survival, which can be targeted and may open up a novel treatment option for HCC in the future. SAGE Publications 2019-08-23 /pmc/articles/PMC6710815/ /pubmed/31489034 http://dx.doi.org/10.1177/1758835919866960 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Hua, Xiangwei Sanjiv, Kumar Gad, Helge Pham, Therese Gokturk, Camilla Rasti, Azita Zhao, Zhenjun He, Kang Feng, Mingxuan Zang, Yunjin Zhang, Jianjun Xia, Qiang Helleday, Thomas Warpman Berglund, Ulrika Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title | Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title_full | Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title_fullStr | Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title_full_unstemmed | Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title_short | Karonudib is a promising anticancer therapy in hepatocellular carcinoma |
title_sort | karonudib is a promising anticancer therapy in hepatocellular carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710815/ https://www.ncbi.nlm.nih.gov/pubmed/31489034 http://dx.doi.org/10.1177/1758835919866960 |
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