Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784609459096518656 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8641200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT verbekes gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT perretr gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT chairev gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT richarde gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT velascov gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT gilesf gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT cavalcantel gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas AT italianoa gsk3betaasacandidatetherapeutictargetinsofttissuesarcomas |