# 5,7-Dihydroxy-4-Methylcoumarin as a Functional Compound for Skin Pigmentation and Human Skin Safety

**Authors:** Ye-Jin Lee, Yang Xu, Chang-Gu Hyun

PMC · DOI: 10.3390/ph18040463 · Pharmaceuticals · 2025-03-25

## TL;DR

This study shows that 5,7-dihydroxy-4-methylcoumarin boosts melanin production and is safe for skin use, making it a potential treatment for pigmentation disorders.

## Contribution

The study introduces 5,7-dihydroxy-4-methylcoumarin as a novel compound with melanogenic and low-irritation properties for cosmetics and therapies.

## Key findings

- 5,7D-4MC increased melanin production and tyrosinase activity in a dose-dependent manner.
- The compound activated PKA and GSK3β pathways while downregulating PI3K/AKT.
- Human skin irritation tests showed low irritation at 50 µM and 100 µM concentrations.

## Abstract

Background/Objectives: This study aims to investigate the effects of 5,7-dihydroxy-4-methylcoumarin (5,7D-4MC) on melanogenesis in B16F10 murine melanoma cells and to evaluate its safety as a potential ingredient for functional cosmetics and therapeutic agents targeting pigmentation-related disorders. Method: The cytotoxicity of 5,7D-4MC was assessed using an MTT assay, and melanin content and tyrosinase activity were measured at different concentrations (25, 50, 100 µM). Western blot analyses were conducted to evaluate the expression of key melanogenesis-related proteins (TYR, TRP-1, TRP-2, and MITF) and to investigate the regulation of major signaling pathways, including PKA/cAMP, GSK3β, and PI3K/AKT. Additionally, a human primary skin irritation test was performed on 32 participants to assess the dermatological safety of 5,7D-4MC. Results: 5,7D-4MC did not affect cell viability at concentrations below 100 µM and significantly promoted melanin production in a dose-dependent manner. Tyrosinase activity and the expression levels of melanogenic proteins increased significantly following 5,7D-4MC treatment. PKA and GSK3β pathways were activated, while the PI3K/AKT pathway was downregulated. The skin irritation test showed that 5,7D-4MC exhibited low irritation potential at concentrations of 50 µM and 100 µM. Conclusions: 5,7D-4MC enhances melanogenesis and demonstrates low skin irritation, making it a promising candidate for therapeutic applications in treating hypopigmentation disorders, such as vitiligo, as well as a functional cosmetic ingredient. However, further studies involving human melanocytes and clinical trials are required to validate their efficacy.

## Linked entities

- **Proteins:** TYR (tyrosinase), PRSS1 (serine protease 1), DCT (dopachrome tautomerase), MITF (melanocyte inducing transcription factor), PKA (cAMP dependent protein kinase), GSK3B (glycogen synthase kinase 3 beta), PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1)
- **Chemicals:** 5,7-dihydroxy-4-methylcoumarin (PubChem CID 5354284), doxorubicin (PubChem CID 31703)
- **Diseases:** vitiligo (MONDO:0008661)

## Full-text entities

- **Genes:** MITF (melanocyte inducing transcription factor) [NCBI Gene 4286] {aka CMM8, COMMAD, MI, MITF-A, WS2, WS2A}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, TYR (tyrosinase) [NCBI Gene 7299] {aka ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3}, DCT (dopachrome tautomerase) [NCBI Gene 1638] {aka OCA8, TRP-2, TYRP2}, TYRP1 (tyrosinase related protein 1) [NCBI Gene 7306] {aka CAS2, CATB, GP75, OCA3, TRP, TRP1}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932]
- **Diseases:** melanoma (MESH:D008545), pigmentation-related disorders (MESH:D010859), skin irritation (MESH:D012871), cytotoxicity (MESH:D064420), vitiligo (MESH:D014820), hypopigmentation disorders (MESH:D017496)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** B16F10 — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_0159)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12030699/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12030699/full.md

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Source: https://tomesphere.com/paper/PMC12030699