Identification of Potential Biomarkers for Ulcerative Colitis and Analysis of Immune Cell Infiltration: A Study Based on Data-Independent Acquisition Proteomics and the GEO Public Database.
- 1Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
- 2Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Abstract
Background
Ulcerative colitis (UC) is a challenging inflammatory bowel disease characterized by chronic inflammation of the colon's mucosal layer. Despite advances in medical research, UC lacks definitive diagnostic tests and targeted treatments.Aims
This study aimed to preliminarily explore non-invasive potential biomarkers for UC based on proteomic analysis and publicly available GEO datasets.Materials & methods
Bioinformatics analyses including ssGSEA for immune infiltration assessment, Spearman correlation analysis, ROC analysis, GSEA, and in silico drug prediction were performed.Results
Four candidate hub genes (KRT17, TCEA3, ACP5, and ACOT13) were identified. ROC analysis demonstrated their potential clinical diagnostic value, and GSEA revealed their association with inflammatory pathways. A total of 28 potential compounds targeting these biomarkers were predicted, among which cinacalcet was selected as a priority candidate drug for further research.Conclusion
The identified hub genes have the potential to act as non-invasive candidate biomarkers for the early diagnosis of UC.
Related
- Identification of potential biomarkers for ulcerative colitis based on multidimensional data analysis and investigation of the mechanisms of therapeutic effects
- Identification of functional genes and immune cell infiltration analysis in liposarcoma
- Identification of CLOCK and MARK2 as Candidate Blood-Based Biomarkers in Type 2 Diabetes: An Integrated Bulk and Single-Cell Transcriptomic Study
- Identification of meat spoilage gene biomarkers in Pseudomonas putida using gene profiling
- Development of immunological reagents for the identification of biomarkers of inflammation in the common marmoset
BibTeX
@article{wang2026identification,
title = {{Identification of Potential Biomarkers for Ulcerative Colitis and Analysis of Immune Cell Infiltration: A Study Based on Data-Independent Acquisition Proteomics and the GEO Public Database.}},
author = {Shuai Wang and Hualiang Deng and Dajuan Sun},
journal = {Proteomics. Clinical applications},
year = {2026},
month = nov,
doi = {10.1002/prca.70061},
url = {https://europepmc.org/article/MED/42974952},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Identification of Potential Biomarkers for Ulcerative Colitis and Analysis of Immune Cell Infiltration: A Study Based on Data-Independent Acquisition Proteomics and the GEO Public Database.
AU - Shuai Wang
AU - Hualiang Deng
AU - Dajuan Sun
PY - 2026
DA - 2026/11/01
JO - Proteomics. Clinical applications
DO - 10.1002/prca.70061
UR - https://europepmc.org/article/MED/42974952
AB - Background Ulcerative colitis (UC) is a challenging inflammatory bowel disease characterized by chronic inflammation of the colon's mucosal layer. Despite advances in medical research, UC lacks definitive diagnostic tests and targeted treatments.Aims This study aimed to preliminarily explore non-invasive potential biomarkers for UC based on proteomic analysis and publicly available GEO datasets.Materials & methods Bioinformatics analyses including ssGSEA for immune infiltration assessment, Spearman correlation analysis, ROC analysis, GSEA, and in silico drug prediction were performed.Results Four candidate hub genes (KRT17, TCEA3, ACP5, and ACOT13) were identified. ROC analysis demonstrated their potential clinical diagnostic value, and GSEA revealed their association with inflammatory pathways. A total of 28 potential compounds targeting these biomarkers were predicted, among which cinacalcet was selected as a priority candidate drug for further research.Conclusion The identified hub genes have the potential to act as non-invasive candidate biomarkers for the early diagnosis of UC.
SN - 1862-8346
SN - 1862-8354
ER -