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Updated: Jun 13, 2026

Studying Chronic Exposure of Mice to Ultraviolet B Radiation
Published on: August 19, 2025
Chemopreventive effects of honokiol on UVB-induced skin cancer development
Shivani Chilampalli1, Xiaoying Zhang, Hesham Fahmy
1Distinguished Professor and Head, Department of Pharmaceutical Sciences, College of Pharmacy-Box 2202 C, 116 A Intramural Building, South Dakota State University, Brookings, SD 57007, USA.
Background:
Skin cancer is the most prevalent of all cancer types and its incidence is expected to increase substantially. Chemoprevention involves the administration of chemical agents to prevent initiation, promotion and/or progression that occurs during neoplastic development. Honokiol, a plant lignan isolated from bark and seed cones of Magnolia officinalis, has been shown to have chemopreventive effects on chemically induced skin cancer development.
Aim:
The objective of this investigation was to study the chemopreventive effects of honokiol on UVB-induced skin tumor development in SKH-1 mice, a model relevant to humans, and to elucidate the possible role of apoptotic proteins involved in the prevention of skin tumor development.
Materials And Methods:
Female SKH-1 mice were divided into two groups. Group 1 received acetone (0.2 ml, topical) and Group 2 received honokiol (30 microg in 0.2 ml acetone, topical) one hour before UVB treatment. Tumor initiation and promotion were carried out by UVB radiation (30 mJ/cm(2)/day), 5 days a week for 30 weeks. Tumor counts and mouse weights were taken weekly.
Results:
The honokiol-pretreated group exhibited a 45% reduction in tumor multiplicity as compared to the control group. Mechanistic studies showed the possible involvement of caspase-3, caspase-8, caspase-9, poly (ADP-ribose) polymerase (PARP) and p53 activation (p<0.05) leading to the induction of DNA fragmentation and apoptosis.
Conclusion:
Pretreatment with honokiol, at concentrations in micrograms per application compared with milligram applications of other potential chemopreventive agents, prevents UVB-induced skin cancer development, possibly by activating proapoptotic proteins through both intrinsic and extrinsic pathways.
Insights
Honokiol effectively prevents UVB-induced skin cancer in mice by activating apoptotic proteins. This natural compound shows promise as a chemopreventive agent for skin cancer.
Area of Science:
- Oncology
- Dermatology
- Natural Products Chemistry
Background:
- Skin cancer is a prevalent malignancy with increasing incidence.
- Chemoprevention strategies aim to inhibit cancer development using chemical agents.
- Honokiol, a lignan from Magnolia officinalis, exhibits chemopreventive properties.
Purpose of the Study:
- To evaluate honokiol's chemopreventive effects against UVB-induced skin tumors in SKH-1 mice.
- To investigate the role of apoptotic proteins in honokiol-mediated skin cancer prevention.
Main Methods:
- SKH-1 mice were topically treated with honokiol or acetone before UVB exposure.
- UVB radiation was administered for 30 weeks to induce skin tumors.
- Tumor multiplicity and mouse weights were monitored weekly.
Main Results:
- Honokiol pretreatment reduced tumor multiplicity by 45% compared to controls.
- Mechanistic studies revealed activation of caspase-3, -8, -9, PARP, and p53.
- These activations led to DNA fragmentation and apoptosis induction.
Conclusions:
- Honokiol pretreatment prevents UVB-induced skin cancer development in a mouse model.
- The mechanism involves the activation of proapoptotic proteins via intrinsic and extrinsic pathways.
- Low-dose honokiol offers a potential chemopreventive strategy for skin cancer.
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