Cargando…

Identification of a mesenchymal-related signature associated with clinical prognosis in glioma

Malignant glioma with a mesenchymal (MES) signature is characterized by shorter survival time due to aggressive dissemination and resistance to chemoradiotherapy. Here, this study used the TCGA database as the training set and the CGGA database as the testing set. Consensus clustering was performed...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Zhengwei, Chen, Jie, Huo, Xiuhao, Zong, Gang, Huang, Kebing, Cheng, Meng, Sun, Libo, Yue, Xiaoyu, Bian, Erbao, Zhao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148476/
https://www.ncbi.nlm.nih.gov/pubmed/33875619
http://dx.doi.org/10.18632/aging.202886
_version_ 1783697847014653952
author Zhang, Zhengwei
Chen, Jie
Huo, Xiuhao
Zong, Gang
Huang, Kebing
Cheng, Meng
Sun, Libo
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
author_facet Zhang, Zhengwei
Chen, Jie
Huo, Xiuhao
Zong, Gang
Huang, Kebing
Cheng, Meng
Sun, Libo
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
author_sort Zhang, Zhengwei
collection PubMed
description Malignant glioma with a mesenchymal (MES) signature is characterized by shorter survival time due to aggressive dissemination and resistance to chemoradiotherapy. Here, this study used the TCGA database as the training set and the CGGA database as the testing set. Consensus clustering was performed on the two data sets, and it was found that two groups had distinguished prognostic and molecular features. Cox analysis and Lasso regression analysis were used to construct MES signature-based risk score model of glioma. Our results show that MES signature-based risk score model can be used to assess the prognosis of glioma. Three methods (ROC curve analyses, univariate Cox regression analysis, multivariate Cox regression analysis) were used to investigate the prognostic role of texture parameters. The result showed that the MES-related gene signature was proved to be an independent prognostic factor for glioma. Furthermore, functional analysis of the gene related to the risk signature showed that the genes sets were closely related to the malignant process of tumors. Finally, FCGR2A and EHD2 were selected for functional verification. Silencing these two genes inhibited the proliferation, migration and invasion of gliomas and reduced the expression of mesenchymal marker genes. Collectively, MES-related risk signature seems to provide a novel target for predicting the prognosis and treatment of glioma.
format Online
Article
Text
id pubmed-8148476
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Impact Journals
record_format MEDLINE/PubMed
spelling pubmed-81484762021-05-26 Identification of a mesenchymal-related signature associated with clinical prognosis in glioma Zhang, Zhengwei Chen, Jie Huo, Xiuhao Zong, Gang Huang, Kebing Cheng, Meng Sun, Libo Yue, Xiaoyu Bian, Erbao Zhao, Bing Aging (Albany NY) Research Paper Malignant glioma with a mesenchymal (MES) signature is characterized by shorter survival time due to aggressive dissemination and resistance to chemoradiotherapy. Here, this study used the TCGA database as the training set and the CGGA database as the testing set. Consensus clustering was performed on the two data sets, and it was found that two groups had distinguished prognostic and molecular features. Cox analysis and Lasso regression analysis were used to construct MES signature-based risk score model of glioma. Our results show that MES signature-based risk score model can be used to assess the prognosis of glioma. Three methods (ROC curve analyses, univariate Cox regression analysis, multivariate Cox regression analysis) were used to investigate the prognostic role of texture parameters. The result showed that the MES-related gene signature was proved to be an independent prognostic factor for glioma. Furthermore, functional analysis of the gene related to the risk signature showed that the genes sets were closely related to the malignant process of tumors. Finally, FCGR2A and EHD2 were selected for functional verification. Silencing these two genes inhibited the proliferation, migration and invasion of gliomas and reduced the expression of mesenchymal marker genes. Collectively, MES-related risk signature seems to provide a novel target for predicting the prognosis and treatment of glioma. Impact Journals 2021-04-19 /pmc/articles/PMC8148476/ /pubmed/33875619 http://dx.doi.org/10.18632/aging.202886 Text en Copyright: © 2021 Zhang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Zhengwei
Chen, Jie
Huo, Xiuhao
Zong, Gang
Huang, Kebing
Cheng, Meng
Sun, Libo
Yue, Xiaoyu
Bian, Erbao
Zhao, Bing
Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title_full Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title_fullStr Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title_full_unstemmed Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title_short Identification of a mesenchymal-related signature associated with clinical prognosis in glioma
title_sort identification of a mesenchymal-related signature associated with clinical prognosis in glioma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148476/
https://www.ncbi.nlm.nih.gov/pubmed/33875619
http://dx.doi.org/10.18632/aging.202886
work_keys_str_mv AT zhangzhengwei identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT chenjie identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT huoxiuhao identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT zonggang identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT huangkebing identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT chengmeng identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT sunlibo identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT yuexiaoyu identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT bianerbao identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma
AT zhaobing identificationofamesenchymalrelatedsignatureassociatedwithclinicalprognosisinglioma