Identification and validation of five ferroptosis-related molecular signatures in keloids based on multiple transcriptome data analysis
- Zhen Sun 1, Yonghong Qin 1, Xuanfen Zhang 1
- Zhen Sun 1, Yonghong Qin 1, Xuanfen Zhang 1
- 1Department of Plastic Surgery, Second Hospital and Clinical Medical School, Lanzhou University, Lanzhou, China.
- 0Department of Plastic Surgery, Second Hospital and Clinical Medical School, Lanzhou University, Lanzhou, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies key ferroptosis-related genes involved in keloid formation, offering potential new biomarkers and therapeutic targets for this common skin disorder.
Area Of Science
- Dermatology
- Molecular Biology
- Genetics
Background
- Keloids are characterized by excessive fibrous tissue growth.
- Ferroptosis, a regulated cell death pathway, is implicated in fibrosis but its role in keloids is unclear.
Purpose Of The Study
- To identify key ferroptosis-related genes in keloid formation.
- To explore their potential as biomarkers or therapeutic targets.
Main Methods
- Analysis of NCBI GEO datasets (GSE145725, GSE7890, GSE44270, GSE181316).
- Identification of differentially expressed and ferroptosis-related genes using LASSO regression.
- Validation via qRT-PCR and Western blot.
Main Results
- Identified 471 differentially expressed genes; selected five key ferroptosis-related genes.
- Two genes were upregulated, three downregulated in keloid tissue.
- These genes are involved in fibrotic processes, confirmed by validation.
Conclusions
- Novel insights into ferroptosis mechanisms in keloid pathogenesis.
- Identified ferroptosis genes may serve as potential keloid biomarkers or therapeutic targets.
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