Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma

Abstract Background Tissue inhibitors of metalloproteinase (TIMP) family proteins are peptidases involved in extracellular matrix (ECM) degradation. Various diseases are related to TIMPs, and the primary reason is that TIMPs can indirectly regulate remodelling of the ECM and cell signalling by regul...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Jinkun Han, Yajun Jing, Fubing Han, Peng Sun
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Acceso en línea:https://doaj.org/article/8594ef83a918433bb13445844b10a59e
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8594ef83a918433bb13445844b10a59e
record_format dspace
spelling oai:doaj.org-article:8594ef83a918433bb13445844b10a59e2021-11-21T12:09:34ZComprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma10.1186/s12883-021-02477-11471-2377https://doaj.org/article/8594ef83a918433bb13445844b10a59e2021-11-01T00:00:00Zhttps://doi.org/10.1186/s12883-021-02477-1https://doaj.org/toc/1471-2377Abstract Background Tissue inhibitors of metalloproteinase (TIMP) family proteins are peptidases involved in extracellular matrix (ECM) degradation. Various diseases are related to TIMPs, and the primary reason is that TIMPs can indirectly regulate remodelling of the ECM and cell signalling by regulating matrix metalloproteinase (MMP) activity. However, the link between TIMPs and glioblastoma (GBM) is unclear. Objective This study aimed to explore the role of TIMP expression and immune infiltration in GBM. Methods Oncomine, GEPIA, OSgbm, LinkedOmics, STRING, GeneMANIA, Enrichr, and TIMER were used to conduct differential expression, prognosis, and immune infiltration analyses of TIMPs in GBM. Results All members of the TIMP family had significantly higher expression levels in GBM. High TIMP3 expression correlated with better overall survival (OS) and disease-specific survival (DSS) in GBM patients. TIMP4 was associated with a long OS in GBM patients. We found a positive relationship between TIMP3 and TIMP4, identifying gene sets with similar or opposite expression directions to those in GBM patients. TIMPs and associated genes are mainly associated with extracellular matrix organization and involve proteoglycan pathways in cancer. The expression levels of TIMPs in GBM correlate with the infiltration of various immune cells, including CD4+ T cells, macrophages, neutrophils, B cells, CD8+ T cells, and dendritic cells. Conclusions Our study inspires new ideas for the role of TIMPs in GBM and provides new directions for multiple treatment modalities, including immunotherapy, in GBM.Jinkun HanYajun JingFubing HanPeng SunBMCarticleBioinformatics analysisTissue inhibitors of metalloproteinases familyGlioblastomaBiomarkerPrognosisImmune infiltrationNeurology. Diseases of the nervous systemRC346-429ENBMC Neurology, Vol 21, Iss 1, Pp 1-15 (2021)
institution DOAJ
collection DOAJ
language EN
topic Bioinformatics analysis
Tissue inhibitors of metalloproteinases family
Glioblastoma
Biomarker
Prognosis
Immune infiltration
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Bioinformatics analysis
Tissue inhibitors of metalloproteinases family
Glioblastoma
Biomarker
Prognosis
Immune infiltration
Neurology. Diseases of the nervous system
RC346-429
Jinkun Han
Yajun Jing
Fubing Han
Peng Sun
Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
description Abstract Background Tissue inhibitors of metalloproteinase (TIMP) family proteins are peptidases involved in extracellular matrix (ECM) degradation. Various diseases are related to TIMPs, and the primary reason is that TIMPs can indirectly regulate remodelling of the ECM and cell signalling by regulating matrix metalloproteinase (MMP) activity. However, the link between TIMPs and glioblastoma (GBM) is unclear. Objective This study aimed to explore the role of TIMP expression and immune infiltration in GBM. Methods Oncomine, GEPIA, OSgbm, LinkedOmics, STRING, GeneMANIA, Enrichr, and TIMER were used to conduct differential expression, prognosis, and immune infiltration analyses of TIMPs in GBM. Results All members of the TIMP family had significantly higher expression levels in GBM. High TIMP3 expression correlated with better overall survival (OS) and disease-specific survival (DSS) in GBM patients. TIMP4 was associated with a long OS in GBM patients. We found a positive relationship between TIMP3 and TIMP4, identifying gene sets with similar or opposite expression directions to those in GBM patients. TIMPs and associated genes are mainly associated with extracellular matrix organization and involve proteoglycan pathways in cancer. The expression levels of TIMPs in GBM correlate with the infiltration of various immune cells, including CD4+ T cells, macrophages, neutrophils, B cells, CD8+ T cells, and dendritic cells. Conclusions Our study inspires new ideas for the role of TIMPs in GBM and provides new directions for multiple treatment modalities, including immunotherapy, in GBM.
format article
author Jinkun Han
Yajun Jing
Fubing Han
Peng Sun
author_facet Jinkun Han
Yajun Jing
Fubing Han
Peng Sun
author_sort Jinkun Han
title Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
title_short Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
title_full Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
title_fullStr Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
title_full_unstemmed Comprehensive analysis of expression, prognosis and immune infiltration for TIMPs in glioblastoma
title_sort comprehensive analysis of expression, prognosis and immune infiltration for timps in glioblastoma
publisher BMC
publishDate 2021
url https://doaj.org/article/8594ef83a918433bb13445844b10a59e
work_keys_str_mv AT jinkunhan comprehensiveanalysisofexpressionprognosisandimmuneinfiltrationfortimpsinglioblastoma
AT yajunjing comprehensiveanalysisofexpressionprognosisandimmuneinfiltrationfortimpsinglioblastoma
AT fubinghan comprehensiveanalysisofexpressionprognosisandimmuneinfiltrationfortimpsinglioblastoma
AT pengsun comprehensiveanalysisofexpressionprognosisandimmuneinfiltrationfortimpsinglioblastoma
_version_ 1718419196767895552