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Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer

Glycogen synthase kinase-3 (GSK-3), a serine/threonine kinase, is involved in a broad range of pathological processes including cancer. GSK-3 has two isoforms, GSK-3α and GSK-3β, and GSK-3β has been recognized as a therapeutic target for the development of new anticancer drugs. The present study aim...

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Autores principales: Anraku, Tsutomu, Kuroki, Hiroo, Kazama, Akira, Bilim, Vladimir, Tasaki, Masaaki, Schmitt, Daniel, Mazar, Andrew, Giles, Francis J., Ugolkov, Andrey, Tomita, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984786/
https://www.ncbi.nlm.nih.gov/pubmed/31894292
http://dx.doi.org/10.3892/ijmm.2019.4427
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author Anraku, Tsutomu
Kuroki, Hiroo
Kazama, Akira
Bilim, Vladimir
Tasaki, Masaaki
Schmitt, Daniel
Mazar, Andrew
Giles, Francis J.
Ugolkov, Andrey
Tomita, Yoshihiko
author_facet Anraku, Tsutomu
Kuroki, Hiroo
Kazama, Akira
Bilim, Vladimir
Tasaki, Masaaki
Schmitt, Daniel
Mazar, Andrew
Giles, Francis J.
Ugolkov, Andrey
Tomita, Yoshihiko
author_sort Anraku, Tsutomu
collection PubMed
description Glycogen synthase kinase-3 (GSK-3), a serine/threonine kinase, is involved in a broad range of pathological processes including cancer. GSK-3 has two isoforms, GSK-3α and GSK-3β, and GSK-3β has been recognized as a therapeutic target for the development of new anticancer drugs. The present study aimed to investigate the antitumor effects of 9-ING-41, which is a maleimide-based ATP-competitive small molecule GSK-3β inhibitor active in patients with advanced cancer. In renal cancer cell lines, treatment with 9-ING-41 alone induced cell cycle arrest and apoptosis, and autophagy inhibitors increased the antitumor effects of 9-ING-41 when used in combination. Treatment with 9-ING-41 potentiated the antitumor effects of targeted therapeutics and increased the cytotoxic effects of cytokine-activated immune cells on renal cancer cell lines. These results provided a compelling rationale for the inclusion of patients with renal cancer in studies of 9-ING-41, both as a single agent and in combination with current standard therapies.
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spelling pubmed-69847862020-02-04 Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer Anraku, Tsutomu Kuroki, Hiroo Kazama, Akira Bilim, Vladimir Tasaki, Masaaki Schmitt, Daniel Mazar, Andrew Giles, Francis J. Ugolkov, Andrey Tomita, Yoshihiko Int J Mol Med Articles Glycogen synthase kinase-3 (GSK-3), a serine/threonine kinase, is involved in a broad range of pathological processes including cancer. GSK-3 has two isoforms, GSK-3α and GSK-3β, and GSK-3β has been recognized as a therapeutic target for the development of new anticancer drugs. The present study aimed to investigate the antitumor effects of 9-ING-41, which is a maleimide-based ATP-competitive small molecule GSK-3β inhibitor active in patients with advanced cancer. In renal cancer cell lines, treatment with 9-ING-41 alone induced cell cycle arrest and apoptosis, and autophagy inhibitors increased the antitumor effects of 9-ING-41 when used in combination. Treatment with 9-ING-41 potentiated the antitumor effects of targeted therapeutics and increased the cytotoxic effects of cytokine-activated immune cells on renal cancer cell lines. These results provided a compelling rationale for the inclusion of patients with renal cancer in studies of 9-ING-41, both as a single agent and in combination with current standard therapies. D.A. Spandidos 2020-02 2019-12-12 /pmc/articles/PMC6984786/ /pubmed/31894292 http://dx.doi.org/10.3892/ijmm.2019.4427 Text en Copyright: © Anraku et al. 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
Anraku, Tsutomu
Kuroki, Hiroo
Kazama, Akira
Bilim, Vladimir
Tasaki, Masaaki
Schmitt, Daniel
Mazar, Andrew
Giles, Francis J.
Ugolkov, Andrey
Tomita, Yoshihiko
Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title_full Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title_fullStr Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title_full_unstemmed Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title_short Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
title_sort clinically relevant gsk-3β inhibitor 9-ing-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984786/
https://www.ncbi.nlm.nih.gov/pubmed/31894292
http://dx.doi.org/10.3892/ijmm.2019.4427
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