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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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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. |
format | Online Article Text |
id | pubmed-6984786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
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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