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Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells

Transforming growth factor-β1 (TGF-β1) potently inhibits human hepatocellular carcinoma (HCC) cell growth. Here we demonstrated that TGF-β1-induced apoptosis is mediated by decreased phosphorylation of cdc2 at Tyr15 accompanied by down-regulation of Wee1 kinase expression. As expected from these res...

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Detalles Bibliográficos
Autores principales: Kogiso, Tomomi, Nagahara, Hikaru, Hashimoto, Etsuko, Ariizumi, Shunichi, Yamamoto, Masakazu, Shiratori, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069002/
https://www.ncbi.nlm.nih.gov/pubmed/24960176
http://dx.doi.org/10.1371/journal.pone.0100495
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author Kogiso, Tomomi
Nagahara, Hikaru
Hashimoto, Etsuko
Ariizumi, Shunichi
Yamamoto, Masakazu
Shiratori, Keiko
author_facet Kogiso, Tomomi
Nagahara, Hikaru
Hashimoto, Etsuko
Ariizumi, Shunichi
Yamamoto, Masakazu
Shiratori, Keiko
author_sort Kogiso, Tomomi
collection PubMed
description Transforming growth factor-β1 (TGF-β1) potently inhibits human hepatocellular carcinoma (HCC) cell growth. Here we demonstrated that TGF-β1-induced apoptosis is mediated by decreased phosphorylation of cdc2 at Tyr15 accompanied by down-regulation of Wee1 kinase expression. As expected from these results, a Wee1 kinase inhibitor efficiently induced apoptosis in HCC cells in the absence of TGF-β1 treatment. In surgically resected samples, Wee1 kinase was expressed in moderately to poorly differentiated HCC, whereas no Wee1 kinase expression was observed in non-cancerous tissue, including cirrhotic tissue. Our results suggest that Wee1 kinase inhibitors may be a practical novel therapeutic option against advanced HCC.
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spelling pubmed-40690022014-06-27 Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells Kogiso, Tomomi Nagahara, Hikaru Hashimoto, Etsuko Ariizumi, Shunichi Yamamoto, Masakazu Shiratori, Keiko PLoS One Research Article Transforming growth factor-β1 (TGF-β1) potently inhibits human hepatocellular carcinoma (HCC) cell growth. Here we demonstrated that TGF-β1-induced apoptosis is mediated by decreased phosphorylation of cdc2 at Tyr15 accompanied by down-regulation of Wee1 kinase expression. As expected from these results, a Wee1 kinase inhibitor efficiently induced apoptosis in HCC cells in the absence of TGF-β1 treatment. In surgically resected samples, Wee1 kinase was expressed in moderately to poorly differentiated HCC, whereas no Wee1 kinase expression was observed in non-cancerous tissue, including cirrhotic tissue. Our results suggest that Wee1 kinase inhibitors may be a practical novel therapeutic option against advanced HCC. Public Library of Science 2014-06-24 /pmc/articles/PMC4069002/ /pubmed/24960176 http://dx.doi.org/10.1371/journal.pone.0100495 Text en © 2014 Kogiso et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kogiso, Tomomi
Nagahara, Hikaru
Hashimoto, Etsuko
Ariizumi, Shunichi
Yamamoto, Masakazu
Shiratori, Keiko
Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title_full Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title_fullStr Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title_full_unstemmed Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title_short Efficient Induction of Apoptosis by Wee1 Kinase Inhibition in Hepatocellular Carcinoma Cells
title_sort efficient induction of apoptosis by wee1 kinase inhibition in hepatocellular carcinoma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069002/
https://www.ncbi.nlm.nih.gov/pubmed/24960176
http://dx.doi.org/10.1371/journal.pone.0100495
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