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Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment
INTRODUCTION: Glioma stem cells (GSCs) play an important role in glioma recurrence and chemo‐radiotherapy (CRT) resistance. Currently, there is a lack of efficient treatment approaches targeting GSCs. This study aimed to explore the potential personalized treatment of patients with GSC‐enriched glio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627385/ https://www.ncbi.nlm.nih.gov/pubmed/36070228 http://dx.doi.org/10.1111/cns.13956 |
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author | Chen, Bo Zhou, Xiaoxi Yang, Liting Zhou, Hongshu Meng, Ming Wu, Hao Liu, Zhixiong Zhang, Liyang Li, Chuntao |
author_facet | Chen, Bo Zhou, Xiaoxi Yang, Liting Zhou, Hongshu Meng, Ming Wu, Hao Liu, Zhixiong Zhang, Liyang Li, Chuntao |
author_sort | Chen, Bo |
collection | PubMed |
description | INTRODUCTION: Glioma stem cells (GSCs) play an important role in glioma recurrence and chemo‐radiotherapy (CRT) resistance. Currently, there is a lack of efficient treatment approaches targeting GSCs. This study aimed to explore the potential personalized treatment of patients with GSC‐enriched gliomas. METHODS: Single‐cell RNA sequencing (scRNA‐seq) was used to identify the GSC‐related genes. Then, machine learning methods were applied for clustering and validation. The least absolute shrinkage and selection operator (LASSO) and COX regression were used to construct the risk scores. Survival analysis was performed. Additionally, the incidence of chemo‐radiotherapy resistance, immunotherapy status, and tumor treating field (TTF) therapy response were evaluated in high‐ and low‐risk scores groups. RESULTS: Two GSC clusters exhibited significantly different stemness indices, immune microenvironments, and genomic alterations. Based on GSC clusters, 11‐gene GSC risk scores were constructed, which exhibited a high predictive value for prognosis. In terms of therapy, patients with high GSC risk scores had a higher risk of resistance to chemotherapy. TTF therapy can comprehensively inhibit the malignant biological characteristics of the high GSC‐risk‐score gliomas. CONCLUSION: Our study constructed a GSC signature consisting of 11 GSC‐specific genes and identified its prognostic value in gliomas. TTF is a promising therapeutic approach for patients with GSC‐enriched glioma. |
format | Online Article Text |
id | pubmed-9627385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96273852022-11-03 Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment Chen, Bo Zhou, Xiaoxi Yang, Liting Zhou, Hongshu Meng, Ming Wu, Hao Liu, Zhixiong Zhang, Liyang Li, Chuntao CNS Neurosci Ther Original Articles INTRODUCTION: Glioma stem cells (GSCs) play an important role in glioma recurrence and chemo‐radiotherapy (CRT) resistance. Currently, there is a lack of efficient treatment approaches targeting GSCs. This study aimed to explore the potential personalized treatment of patients with GSC‐enriched gliomas. METHODS: Single‐cell RNA sequencing (scRNA‐seq) was used to identify the GSC‐related genes. Then, machine learning methods were applied for clustering and validation. The least absolute shrinkage and selection operator (LASSO) and COX regression were used to construct the risk scores. Survival analysis was performed. Additionally, the incidence of chemo‐radiotherapy resistance, immunotherapy status, and tumor treating field (TTF) therapy response were evaluated in high‐ and low‐risk scores groups. RESULTS: Two GSC clusters exhibited significantly different stemness indices, immune microenvironments, and genomic alterations. Based on GSC clusters, 11‐gene GSC risk scores were constructed, which exhibited a high predictive value for prognosis. In terms of therapy, patients with high GSC risk scores had a higher risk of resistance to chemotherapy. TTF therapy can comprehensively inhibit the malignant biological characteristics of the high GSC‐risk‐score gliomas. CONCLUSION: Our study constructed a GSC signature consisting of 11 GSC‐specific genes and identified its prognostic value in gliomas. TTF is a promising therapeutic approach for patients with GSC‐enriched glioma. John Wiley and Sons Inc. 2022-09-07 /pmc/articles/PMC9627385/ /pubmed/36070228 http://dx.doi.org/10.1111/cns.13956 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Chen, Bo Zhou, Xiaoxi Yang, Liting Zhou, Hongshu Meng, Ming Wu, Hao Liu, Zhixiong Zhang, Liyang Li, Chuntao Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title | Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title_full | Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title_fullStr | Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title_full_unstemmed | Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title_short | Glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
title_sort | glioma stem cell signature predicts the prognosis and the response to tumor treating fields treatment |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627385/ https://www.ncbi.nlm.nih.gov/pubmed/36070228 http://dx.doi.org/10.1111/cns.13956 |
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