# Lipid metabolism dysregulation in solar lentigo: a multi-system-level analysis reveals membrane instability and energy homeostasis disruption

**Authors:** Sohyun Kim, Wonmin Lee, Junghyun Kim, Yoonsung Lee, Kiwon Lee, Man S. Kim, Soon-Hyo Kwon

PMC · DOI: 10.3389/fcell.2026.1751543 · Frontiers in Cell and Developmental Biology · 2026-03-02

## TL;DR

This study finds that solar lentigo involves disrupted lipid metabolism, leading to membrane instability and energy issues in the skin.

## Contribution

The study reveals novel lipid metabolism dysregulation in solar lentigo beyond melanogenesis, identifying potential therapeutic targets.

## Key findings

- Solar lentigo samples show inhibited fatty acid elongation and sphingolipid biosynthesis.
- Cholesterol synthesis is impaired due to reduced squalene epoxidase and 7-dehydrocholesterol reductase activity.
- Phospholipid synthesis enzymes and dihydroceramide desaturases are compensatorily upregulated.

## Abstract

Solar lentigo is a common hyperpigmented skin condition caused by chronic ultraviolet exposure, primarily affecting photoaged skin. While previous investigations focused on inflammatory and melanogenic mechanisms, the comprehensive role of lipid metabolism in pathogenesis remains unclear. We aimed to investigate systemic alterations in lipid metabolism and their contribution to solar lentigo development. We performed comprehensive analysis of RNA sequencing data from solar lentigo lesions and control skin samples (n = 7 per group) using metabolic flux simulations, gene co-expression networks, and protein-protein interaction analysis. These multi-system approaches were integrated to identify coordinated alterations in lipid metabolic pathways. Solar lentigo samples exhibited coordinated inhibition of fatty acid elongation, acetyl-CoA carboxylase activity, and sphingolipid biosynthesis, alongside impaired cholesterol synthesis via reduced squalene epoxidase and 7-dehydrocholesterol reductase activity. Compensatory upregulation of phospholipid synthesis enzymes and dihydroceramide desaturases was observed. Pathway disruption and altered calcium signaling, indicating aberrant cellular energy metabolism and membrane integrity. These findings suggest that solar lentigo pathogenesis involves systematic lipid metabolism dysregulation beyond melanogenesis, potentially contributing to membrane instability, energy homeostasis disruption and redox imbalance. The identification of specific metabolic bottlenecks reveals novel targets for lipid-based therapeutic approaches in pigmentary diseases.

## Linked entities

- **Proteins:** CAC2 (acetyl Co-enzyme a carboxylase biotin carboxylase subunit)

## Full-text entities

- **Genes:** SQLE (squalene epoxidase) [NCBI Gene 6713], DHCR7 (7-dehydrocholesterol reductase) [NCBI Gene 1717] {aka SLOS}
- **Diseases:** pigmentary diseases (MESH:D004194), Solar lentigo (MESH:D007911), inflammatory (MESH:D007249), hyperpigmented skin condition (MESH:D012871)
- **Chemicals:** fatty acid (MESH:D005227), calcium (MESH:D002118), cholesterol (MESH:D002784), Lipid (MESH:D008055), sphingolipid (MESH:D013107), phospholipid (MESH:D010743)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12989492/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12989492/full.md

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Source: https://tomesphere.com/paper/PMC12989492