Integrative analysis of ferroptosis-related genes in ulcerative colitis

Objective The aim of this study was to identify and validate ferroptosis-related markers in ulcerative colitis (UC) to explore new directions for UC diagnosis and treatment. Methods We screened UC chips and ferroptosis-related genes from the Gene Expression Omnibus (GEO), FerrDb, and GeneCards datab...

Full description

Bibliographic Details
Main Authors: De-jun Cui, Chen Chen, Wen-qiang Yuan, Yun-han Yang, Lu Han
Format: Article
Language:English
Published: SAGE Publishing 2021-09-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605211042975
_version_ 1818589114304299008
author De-jun Cui
Chen Chen
Wen-qiang Yuan
Yun-han Yang
Lu Han
author_facet De-jun Cui
Chen Chen
Wen-qiang Yuan
Yun-han Yang
Lu Han
author_sort De-jun Cui
collection DOAJ
description Objective The aim of this study was to identify and validate ferroptosis-related markers in ulcerative colitis (UC) to explore new directions for UC diagnosis and treatment. Methods We screened UC chips and ferroptosis-related genes from the Gene Expression Omnibus (GEO), FerrDb, and GeneCards databases. The differentially expressed genes (DEGs) and ferroptosis-related DEGs between the UC group and normal controls were analyzed using bioinformatics methods. Enrichment analysis, protein–protein interaction analysis, and hub genes were screened. Peripheral blood chip and animal experiments were used to validate the ferroptosis-related hub genes. Finally, hub gene–transcription factor, hub gene–microRNA (miRNA), and hub gene–drug interaction networks were constructed. Results Overall, 26 ferroptosis-related DEGs were identified that were significantly enriched in energy pathways and metabolism. We identified ten ferroptosis-related hub genes from the protein–protein interaction network: IL6 , PTGS2 , HIF1A , CD44 , MUC1 , CAV1 , NOS2 , CXCL2 , SCD , and ACSL4 . In the peripheral blood chip GSE94648, CD44 and MUC1 were upregulated, which was consistent with the expression trend in GSE75214. Animal experiments showed that CD44 expression was significantly increased in the colon. Conclusions Our findings indicate that CD44 and MUC1 may be ferroptosis-related markers in UC.
first_indexed 2024-12-16T09:35:30Z
format Article
id doaj.art-32574de3326d4130ae620f0d262e1069
institution Directory Open Access Journal
issn 1473-2300
language English
last_indexed 2024-12-16T09:35:30Z
publishDate 2021-09-01
publisher SAGE Publishing
record_format Article
series Journal of International Medical Research
spelling doaj.art-32574de3326d4130ae620f0d262e10692022-12-21T22:36:25ZengSAGE PublishingJournal of International Medical Research1473-23002021-09-014910.1177/03000605211042975Integrative analysis of ferroptosis-related genes in ulcerative colitisDe-jun CuiChen ChenWen-qiang YuanYun-han YangLu HanObjective The aim of this study was to identify and validate ferroptosis-related markers in ulcerative colitis (UC) to explore new directions for UC diagnosis and treatment. Methods We screened UC chips and ferroptosis-related genes from the Gene Expression Omnibus (GEO), FerrDb, and GeneCards databases. The differentially expressed genes (DEGs) and ferroptosis-related DEGs between the UC group and normal controls were analyzed using bioinformatics methods. Enrichment analysis, protein–protein interaction analysis, and hub genes were screened. Peripheral blood chip and animal experiments were used to validate the ferroptosis-related hub genes. Finally, hub gene–transcription factor, hub gene–microRNA (miRNA), and hub gene–drug interaction networks were constructed. Results Overall, 26 ferroptosis-related DEGs were identified that were significantly enriched in energy pathways and metabolism. We identified ten ferroptosis-related hub genes from the protein–protein interaction network: IL6 , PTGS2 , HIF1A , CD44 , MUC1 , CAV1 , NOS2 , CXCL2 , SCD , and ACSL4 . In the peripheral blood chip GSE94648, CD44 and MUC1 were upregulated, which was consistent with the expression trend in GSE75214. Animal experiments showed that CD44 expression was significantly increased in the colon. Conclusions Our findings indicate that CD44 and MUC1 may be ferroptosis-related markers in UC.https://doi.org/10.1177/03000605211042975
spellingShingle De-jun Cui
Chen Chen
Wen-qiang Yuan
Yun-han Yang
Lu Han
Integrative analysis of ferroptosis-related genes in ulcerative colitis
Journal of International Medical Research
title Integrative analysis of ferroptosis-related genes in ulcerative colitis
title_full Integrative analysis of ferroptosis-related genes in ulcerative colitis
title_fullStr Integrative analysis of ferroptosis-related genes in ulcerative colitis
title_full_unstemmed Integrative analysis of ferroptosis-related genes in ulcerative colitis
title_short Integrative analysis of ferroptosis-related genes in ulcerative colitis
title_sort integrative analysis of ferroptosis related genes in ulcerative colitis
url https://doi.org/10.1177/03000605211042975
work_keys_str_mv AT dejuncui integrativeanalysisofferroptosisrelatedgenesinulcerativecolitis
AT chenchen integrativeanalysisofferroptosisrelatedgenesinulcerativecolitis
AT wenqiangyuan integrativeanalysisofferroptosisrelatedgenesinulcerativecolitis
AT yunhanyang integrativeanalysisofferroptosisrelatedgenesinulcerativecolitis
AT luhan integrativeanalysisofferroptosisrelatedgenesinulcerativecolitis