Methylation of LINE-1 and Alu repetitive sequence in keloid

Keloid is a trauma-induced fibroproliferative condition characterized by excessive extracellular matrix (ECM) deposition and aberrant keloid fibroblast activation, leading to physical, psychological, functional, and cosmetic impairments. This study investigates DNA methylation alterations at Long Interspersed Nuclear Element-1 (LINE-1) and Alu repetitive elements in keloid tissues compared to normal skin tissues. Methylation levels and patterns were analyzed in keloid (n = 38) and normal skin tissues (n = 32). The results revealed significantly lower LINE-1 (P < 0.0001) and Alu (P = 0.0147) methylation levels in keloids, with hypomethylation inversely correlated with chronological age. Younger individuals exhibited higher methylation levels compared to older individuals. These findings offer critical insights into the epigenetic mechanisms underlying keloid formation and progression, providing a foundation for developing epigenetic-based therapeutic strategies.

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Publication Details

Journal
Scientific Reports
Published
2025-08-30
DOI
https://doi.org/10.1038/s41598-025-17646-2
Primary Topic
Dermatologic Treatments and Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Methylation of LINE-1 and Alu repetitive sequence in keloid

Piyawan Prabsattru, Nakarin Kitkumthorn, Jiraroch Meevassana, Tanchanok Nakbua et al.
Scientific Reports
Dermatologic Treatments and Research
article

Methylation of LINE-1 and Alu repetitive sequence in keloid

Piyawan Prabsattru, Nakarin Kitkumthorn, Jiraroch Meevassana, Tanchanok Nakbua, Suthida Sengphairogh
article en

Abstract

Keloid is a trauma-induced fibroproliferative condition characterized by excessive extracellular matrix (ECM) deposition and aberrant keloid fibroblast activation, leading to physical, psychological, functional, and cosmetic impairments. This study investigates DNA methylation alterations at Long Interspersed Nuclear Element-1 (LINE-1) and Alu repetitive elements in keloid tissues compared to normal skin tissues. Methylation levels and patterns were analyzed in keloid (n = 38) and normal skin tissues (n = 32). The results revealed significantly lower LINE-1 (P < 0.0001) and Alu (P = 0.0147) methylation levels in keloids, with hypomethylation inversely correlated with chronological age. Younger individuals exhibited higher methylation levels compared to older individuals. These findings offer critical insights into the epigenetic mechanisms underlying keloid formation and progression, providing a foundation for developing epigenetic-based therapeutic strategies.

Scientific ReportsVol. 15(1)
Chulalongkorn University (TH), Mahidol University (TH)
Chulalongkorn University
Openalex Percentile: Top 60%
Dermatologic Treatments and Research
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