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Updated: Jul 3, 2026

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model
Published on: September 7, 2013
Myricetin suppresses UVB-induced skin cancer by targeting Fyn
Sung Keun Jung1, Ki Won Lee, Sanguine Byun
1Department of Agricultural Biotechnology, Seoul National University, Seoul, Republic of Korea.
Abstract:
Skin cancer is currently the most common type of human cancer in Americans. Myricetin, a naturally occurring phytochemical, has potent anticancer-promoting activity and contributes to the chemopreventive potential of several foods, including red wine. Here, we show that myricetin suppresses UVB-induced cyclooxygenase-2 (COX-2) expression in mouse skin epidermal JB6 P+ cells. The activation of activator protein-1 and nuclear factor-kappaB induced by UVB was dose-dependently inhibited by myricetin treatment. Western blot and kinase assay data revealed that myricetin inhibited Fyn kinase activity and subsequently attenuated UVB-induced phosphorylation of mitogen-activated protein kinases. Pull-down assays revealed that myricetin competitively bound with ATP to suppress Fyn kinase activity. Importantly, myricetin exerted similar inhibitory effects compared with 4-amino-5-(4-chloro-phenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine, a well-known pharmacologic inhibitor of Fyn. In vivo mouse skin data also revealed that myricetin inhibited Fyn kinase activity directly and subsequently attenuated UVB-induced COX-2 expression. Mouse skin tumorigenesis data clearly showed that pretreatment with myricetin significantly suppressed UVB-induced skin tumor incidence in a dose-dependent manner. Docking data suggest that myricetin is easily docked to the ATP-binding site of Fyn, which is located between the N and C lobes of the kinase domain. Overall, these results indicated that myricetin exerts potent chemopreventive activity mainly by targeting Fyn in skin carcinogenesis.
Insights
Myricetin, a natural compound, effectively prevents skin cancer by inhibiting Fyn kinase activity. This phytochemical suppresses UVB-induced inflammation and tumor development, offering a promising chemopreventive strategy.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- Skin cancer is the most common human cancer in Americans.
- Myricetin, a phytochemical found in foods like red wine, shows anticancer-promoting activity.
- Understanding the molecular mechanisms of skin cancer chemoprevention is crucial.
Purpose of the Study:
- To investigate the chemopreventive effects of myricetin against UVB-induced skin carcinogenesis.
- To elucidate the molecular targets and pathways through which myricetin exerts its effects.
- To evaluate myricetin's efficacy in preclinical models of skin cancer.
Main Methods:
- Utilized mouse skin epidermal JB6 P+ cells and in vivo mouse skin models.
- Assessed UVB-induced cyclooxygenase-2 (COX-2) expression, activator protein-1 (AP-1) and nuclear factor-kappaB (NF-κB) activation.
- Performed Western blot, kinase assays, pull-down assays, and molecular docking to analyze Fyn kinase activity and myricetin's interaction.
Main Results:
- Myricetin suppressed UVB-induced COX-2 expression and the activation of AP-1 and NF-κB in a dose-dependent manner.
- Myricetin directly inhibited Fyn kinase activity, attenuating downstream signaling pathways.
- In vivo studies confirmed myricetin's ability to inhibit Fyn kinase and reduce UVB-induced skin tumor incidence.
Conclusions:
- Myricetin demonstrates significant chemopreventive activity against UVB-induced skin carcinogenesis.
- The primary mechanism involves the direct targeting and inhibition of Fyn kinase by myricetin.
- Myricetin represents a promising natural agent for the prevention of skin cancer.
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