Identification of Ferroptosis-Related Genes in Schizophrenia Based on Bioinformatic Analysis

Genes (Basel). 2022 Nov 20;13(11):2168. doi: 10.3390/genes13112168.

Abstract

The purpose of this study is to explore the correlation between ferroptosis-related genes and schizophrenia in order to explore the new direction of diagnosis and treatment of schizophrenia. We screened the datasets related to schizophrenia from the Gene Expression Comprehensive Database (GEO) and obtained ferroptosis-related genes from the FerrDB database. Bioinformatics methods were used to analyze differentially expressed genes (DEGs) and genes associated with ferroptosis-related between schizophrenia patients and healthy controls. On this basis, the hub genes were finally screened by enrichment analysis and PPI interaction analysis. Hub genes associated with ferroptosis were validated using other schizophrenia datasets in the GEO database. Finally, the hub gene-microRNA (miRNA), gene-transcription factor interaction network was constructed, and three ferroptosis-related hub genes (TP53, VEGFA and PTGS2) were screened. The validation results of these three genes in other datasets also support this conclusion. A miRNA: hsa-mir-16-5p was found to be related to the three hub genes, and pPHF8, SAP30 and lKDM5B were identified as common regulators of the three hub genes. Our results indicate that TP53, VEGFA and PTGS2 are significantly associated with schizophrenia, and may be ferroptosis-related markers of the disease.

Keywords: GEO; bioinformatic; ferroptosis; schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Computational Biology
  • Cyclooxygenase 2
  • Ferroptosis* / genetics
  • Humans
  • MicroRNAs* / genetics
  • Schizophrenia* / genetics

Substances

  • Cyclooxygenase 2
  • MicroRNAs

Grants and funding

Shanghai Municipal Science and Technology Major Project (2018SHZDZX05).