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The adaptive transition of glioblastoma stem cells and its implications on treatments
Glioblastoma is the most malignant tumor occurring in the human central nervous system with overall median survival time <14.6 months. Current treatments such as chemotherapy and radiotherapy cannot reach an optimal remission since tumor resistance to therapy remains a challenge. Glioblastoma ste...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985200/ https://www.ncbi.nlm.nih.gov/pubmed/33753720 http://dx.doi.org/10.1038/s41392-021-00491-w |
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author | Wang, Zeyu Zhang, Hao Xu, Shengchao Liu, Zhixiong Cheng, Quan |
author_facet | Wang, Zeyu Zhang, Hao Xu, Shengchao Liu, Zhixiong Cheng, Quan |
author_sort | Wang, Zeyu |
collection | PubMed |
description | Glioblastoma is the most malignant tumor occurring in the human central nervous system with overall median survival time <14.6 months. Current treatments such as chemotherapy and radiotherapy cannot reach an optimal remission since tumor resistance to therapy remains a challenge. Glioblastoma stem cells are considered to be responsible for tumor resistance in treating glioblastoma. Previous studies reported two subtypes, proneural and mesenchymal, of glioblastoma stem cells manifesting different sensitivity to radiotherapy or chemotherapy. Mesenchymal glioblastoma stem cells, as well as tumor cells generate from which, showed resistance to radiochemotherapies. Besides, two metabolic patterns, glutamine or glucose dependent, of mesenchymal glioblastoma stem cells also manifested different sensitivity to radiochemotherapies. Glutamine dependent mesenchymal glioblastoma stem cells are more sensitive to radiotherapy than glucose-dependent ones. Therefore, the transition between proneural and mesenchymal subtypes, or between glutamine-dependent and glucose-dependent, might lead to tumor resistance to radiochemotherapies. Moreover, neural stem cells were also hypothesized to participate in glioblastoma stem cells mediated tumor resistance to radiochemotherapies. In this review, we summarized the basic characteristics, adaptive transition and implications of glioblastoma stem cells in glioblastoma therapy. |
format | Online Article Text |
id | pubmed-7985200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79852002021-04-12 The adaptive transition of glioblastoma stem cells and its implications on treatments Wang, Zeyu Zhang, Hao Xu, Shengchao Liu, Zhixiong Cheng, Quan Signal Transduct Target Ther Review Article Glioblastoma is the most malignant tumor occurring in the human central nervous system with overall median survival time <14.6 months. Current treatments such as chemotherapy and radiotherapy cannot reach an optimal remission since tumor resistance to therapy remains a challenge. Glioblastoma stem cells are considered to be responsible for tumor resistance in treating glioblastoma. Previous studies reported two subtypes, proneural and mesenchymal, of glioblastoma stem cells manifesting different sensitivity to radiotherapy or chemotherapy. Mesenchymal glioblastoma stem cells, as well as tumor cells generate from which, showed resistance to radiochemotherapies. Besides, two metabolic patterns, glutamine or glucose dependent, of mesenchymal glioblastoma stem cells also manifested different sensitivity to radiochemotherapies. Glutamine dependent mesenchymal glioblastoma stem cells are more sensitive to radiotherapy than glucose-dependent ones. Therefore, the transition between proneural and mesenchymal subtypes, or between glutamine-dependent and glucose-dependent, might lead to tumor resistance to radiochemotherapies. Moreover, neural stem cells were also hypothesized to participate in glioblastoma stem cells mediated tumor resistance to radiochemotherapies. In this review, we summarized the basic characteristics, adaptive transition and implications of glioblastoma stem cells in glioblastoma therapy. Nature Publishing Group UK 2021-03-23 /pmc/articles/PMC7985200/ /pubmed/33753720 http://dx.doi.org/10.1038/s41392-021-00491-w Text en © The Author(s) 2021 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Article Wang, Zeyu Zhang, Hao Xu, Shengchao Liu, Zhixiong Cheng, Quan The adaptive transition of glioblastoma stem cells and its implications on treatments |
title | The adaptive transition of glioblastoma stem cells and its implications on treatments |
title_full | The adaptive transition of glioblastoma stem cells and its implications on treatments |
title_fullStr | The adaptive transition of glioblastoma stem cells and its implications on treatments |
title_full_unstemmed | The adaptive transition of glioblastoma stem cells and its implications on treatments |
title_short | The adaptive transition of glioblastoma stem cells and its implications on treatments |
title_sort | adaptive transition of glioblastoma stem cells and its implications on treatments |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985200/ https://www.ncbi.nlm.nih.gov/pubmed/33753720 http://dx.doi.org/10.1038/s41392-021-00491-w |
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