Characterization of an endoplasmic reticulum stress-related signature to evaluate immune features and predict prognosis in glioma

J Cell Mol Med. 2021 Apr;25(8):3870-3884. doi: 10.1111/jcmm.16321. Epub 2021 Feb 21.

Abstract

Endoplasmic reticulum (ER) stress has considerable impact on cell growth, proliferation, metastasis, invasion, angiogenesis and chemoradiotherapy resistance in various cancers. However, the effect of ER stress on the outcomes of glioma patients remains unclear. In this study, we established an ER stress risk model based on The Cancer Genome Atlas (TCGA) glioma data set to reflect immune characteristics and predict the prognosis of glioma patients. Survival analysis indicated that there were significant differences in the overall survival (OS) of glioma patients with different ER stress-related risk scores. Moreover, the ER stress-related risk signature, which was markedly associated with the clinicopathological properties of glioma patients, could serve as an independent prognostic indicator. Functional enrichment analysis revealed that the risk model correlated with immune and inflammation responses, as well as biosynthesis and degradation. In addition, the ER stress-related risk model indicated an immunosuppressive microenvironment. In conclusion, we present an ER stress risk model that is an independent prognostic factor and indicates the general immune characteristics in the glioma microenvironment.

Keywords: endoplasmic reticulum stress; endoplasmic reticulum stress risk model; glioma; immunosuppressive; overall survival; tumour microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Brain Neoplasms / genetics
  • Brain Neoplasms / immunology
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology*
  • Endoplasmic Reticulum Stress*
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic*
  • Glioma / genetics
  • Glioma / immunology
  • Glioma / metabolism
  • Glioma / pathology*
  • Humans
  • Nomograms*
  • Prognosis
  • Risk Factors
  • Survival Rate

Substances

  • Biomarkers, Tumor