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Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma

BACKGROUND: Glioma is the most common brain tumor in adults and is characterized by a short survival time and high resistance to chemotherapy. It is imperative to determine the prognosis and therapy-related targets for glioma. Endoplasmic reticulum stress (ERS), as an adaptive protective mechanism,...

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Autores principales: Li, Lianxin, Yang, Zhihao, Zheng, Yinfei, Chen, Zhigang, Yue, Xiaoyu, Bian, Erbao, Zhao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131635/
https://www.ncbi.nlm.nih.gov/pubmed/35614390
http://dx.doi.org/10.1186/s12883-022-02709-y
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author Li, Lianxin
Yang, Zhihao
Zheng, Yinfei
Chen, Zhigang
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
author_facet Li, Lianxin
Yang, Zhihao
Zheng, Yinfei
Chen, Zhigang
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
author_sort Li, Lianxin
collection PubMed
description BACKGROUND: Glioma is the most common brain tumor in adults and is characterized by a short survival time and high resistance to chemotherapy. It is imperative to determine the prognosis and therapy-related targets for glioma. Endoplasmic reticulum stress (ERS), as an adaptive protective mechanism, indicates the unfolded protein response (UPR) to determine cell survival and affects chemotherapy sensitivity, which is related to the prognosis of glioma. METHODS: Our research used the TCGA database as the training group and the CGGA database as the testing group. Lasso regression and Cox analysis were performed to construct an ERS signature-based risk score model in glioma. Three methods (time-dependent receiver operating characteristic analysis and multivariate and univariate Cox regression analysis) were applied to assess the independent prognostic effect of texture parameters. Consensus clustering was used to classify the two clusters. In addition, functional and immune analyses were performed to assess the malignant process and immune microenvironment. Immunotherapy and anticancer drug response prediction were adopted to evaluate immune checkpoint and chemotherapy sensitivity. RESULTS: The results revealed that the 7-gene signature strongly predicts glioma prognosis. The two clusters have markedly distinct molecular and prognostic features. The validation group result revealed that the signature has exceptional repeatability and certainty. Functional analysis showed that the ERS-related gene signature was closely associated with the malignant process and prognosis of tumors. Immune analysis indicated that the ERS-related gene signature is strongly related to immune infiltration. Immunotherapy and anticancer drug response prediction indicated that the ERS-related gene signature is positively correlated with immune checkpoint and chemotherapy sensitivity. CONCLUSIONS: Collectively, the ERS-related risk model can provide a novel signature to predict glioma prognosis and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02709-y.
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spelling pubmed-91316352022-05-26 Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma Li, Lianxin Yang, Zhihao Zheng, Yinfei Chen, Zhigang Yue, Xiaoyu Bian, Erbao Zhao, Bing BMC Neurol Research BACKGROUND: Glioma is the most common brain tumor in adults and is characterized by a short survival time and high resistance to chemotherapy. It is imperative to determine the prognosis and therapy-related targets for glioma. Endoplasmic reticulum stress (ERS), as an adaptive protective mechanism, indicates the unfolded protein response (UPR) to determine cell survival and affects chemotherapy sensitivity, which is related to the prognosis of glioma. METHODS: Our research used the TCGA database as the training group and the CGGA database as the testing group. Lasso regression and Cox analysis were performed to construct an ERS signature-based risk score model in glioma. Three methods (time-dependent receiver operating characteristic analysis and multivariate and univariate Cox regression analysis) were applied to assess the independent prognostic effect of texture parameters. Consensus clustering was used to classify the two clusters. In addition, functional and immune analyses were performed to assess the malignant process and immune microenvironment. Immunotherapy and anticancer drug response prediction were adopted to evaluate immune checkpoint and chemotherapy sensitivity. RESULTS: The results revealed that the 7-gene signature strongly predicts glioma prognosis. The two clusters have markedly distinct molecular and prognostic features. The validation group result revealed that the signature has exceptional repeatability and certainty. Functional analysis showed that the ERS-related gene signature was closely associated with the malignant process and prognosis of tumors. Immune analysis indicated that the ERS-related gene signature is strongly related to immune infiltration. Immunotherapy and anticancer drug response prediction indicated that the ERS-related gene signature is positively correlated with immune checkpoint and chemotherapy sensitivity. CONCLUSIONS: Collectively, the ERS-related risk model can provide a novel signature to predict glioma prognosis and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02709-y. BioMed Central 2022-05-25 /pmc/articles/PMC9131635/ /pubmed/35614390 http://dx.doi.org/10.1186/s12883-022-02709-y Text en © The Author(s) 2022 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 Research
Li, Lianxin
Yang, Zhihao
Zheng, Yinfei
Chen, Zhigang
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title_full Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title_fullStr Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title_full_unstemmed Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title_short Identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
title_sort identification of an endoplasmic reticulum stress-related signature associated with clinical prognosis and immune therapy in glioma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131635/
https://www.ncbi.nlm.nih.gov/pubmed/35614390
http://dx.doi.org/10.1186/s12883-022-02709-y
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