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GSK3-beta as a candidate therapeutic target in soft tissue sarcomas

Soft tissue sarcoma (STS) is a predominantly fatal rare malignancy with inadequate treatment options. Glycogen synthase kinase 3β (GSK-3β) is an emerging target in human malignancies. Its therapeutic relevance in STS is unknown. We analyzed the prognostic impact of GSK-3β gene and protein expression...

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Autores principales: Verbeke, S., Perret, R., Chaire, V., Richard, E., Velasco, V., Giles, F., Cavalcante, L., Italiano, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641200/
https://www.ncbi.nlm.nih.gov/pubmed/34857030
http://dx.doi.org/10.1186/s13045-021-01215-x
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author Verbeke, S.
Perret, R.
Chaire, V.
Richard, E.
Velasco, V.
Giles, F.
Cavalcante, L.
Italiano, A.
author_facet Verbeke, S.
Perret, R.
Chaire, V.
Richard, E.
Velasco, V.
Giles, F.
Cavalcante, L.
Italiano, A.
author_sort Verbeke, S.
collection PubMed
description Soft tissue sarcoma (STS) is a predominantly fatal rare malignancy with inadequate treatment options. Glycogen synthase kinase 3β (GSK-3β) is an emerging target in human malignancies. Its therapeutic relevance in STS is unknown. We analyzed the prognostic impact of GSK-3β gene and protein expression in two independent cohorts of patients with STS. We then treated STS cell lines and mice xenografts with a novel GSK-3 inhibitor 9-ING-41 alone or in combination with chemotherapy. We demonstrated that 9-ING-41 treatment induced significant STS cells apoptosis and was synergistic in vivo when combined with chemotherapy. Mechanistically, 9-ING-41 induces significant apoptosis of STS cells via suppression of NF-κB-mediated X-linked inhibitor of apoptosis protein (XIAP) expression. These data support the inclusion of patients with STS in clinical studies of 9-ING-41 alone and in combination with chemotherapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01215-x.
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spelling pubmed-86412002021-12-06 GSK3-beta as a candidate therapeutic target in soft tissue sarcomas Verbeke, S. Perret, R. Chaire, V. Richard, E. Velasco, V. Giles, F. Cavalcante, L. Italiano, A. J Hematol Oncol Letter to the Editor Soft tissue sarcoma (STS) is a predominantly fatal rare malignancy with inadequate treatment options. Glycogen synthase kinase 3β (GSK-3β) is an emerging target in human malignancies. Its therapeutic relevance in STS is unknown. We analyzed the prognostic impact of GSK-3β gene and protein expression in two independent cohorts of patients with STS. We then treated STS cell lines and mice xenografts with a novel GSK-3 inhibitor 9-ING-41 alone or in combination with chemotherapy. We demonstrated that 9-ING-41 treatment induced significant STS cells apoptosis and was synergistic in vivo when combined with chemotherapy. Mechanistically, 9-ING-41 induces significant apoptosis of STS cells via suppression of NF-κB-mediated X-linked inhibitor of apoptosis protein (XIAP) expression. These data support the inclusion of patients with STS in clinical studies of 9-ING-41 alone and in combination with chemotherapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01215-x. BioMed Central 2021-12-02 /pmc/articles/PMC8641200/ /pubmed/34857030 http://dx.doi.org/10.1186/s13045-021-01215-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Letter to the Editor
Verbeke, S.
Perret, R.
Chaire, V.
Richard, E.
Velasco, V.
Giles, F.
Cavalcante, L.
Italiano, A.
GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title_full GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title_fullStr GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title_full_unstemmed GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title_short GSK3-beta as a candidate therapeutic target in soft tissue sarcomas
title_sort gsk3-beta as a candidate therapeutic target in soft tissue sarcomas
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641200/
https://www.ncbi.nlm.nih.gov/pubmed/34857030
http://dx.doi.org/10.1186/s13045-021-01215-x
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