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Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA
Published on: December 19, 2019
The enhancing effects of hyperbaric oxygen on mouse skin carcinogenesis
Hiroshi Doguchi1, Masanao Saio1, Shimpei Kuniyoshi1
1Department of Pathology and Oncology, Graduate School of Medicine, University of the Ryukyus, 207 Uehara, Nishihara, Okinawa 903-0125, Japan.
Hyperbaric oxygen (HBO) therapy accelerated tumor cell proliferation and advanced skin cancer progression in mice treated with 7,12-dimethylbenz[a]anthracene (DMBA) and 12-O-tetradecanoylphorbol-13-acetate (TPA). These findings indicate HBO may promote carcinogenesis.
Area of Science:
- Oncology
- Dermatology
- Hyperbaric Medicine
Background:
- Two-stage chemical carcinogenesis is a common model for studying skin cancer development.
- Hyperbaric oxygen (HBO) therapy involves breathing pure oxygen in a pressurized chamber.
- The impact of HBO on chemical carcinogenesis is not fully understood.
Purpose of the Study:
- To investigate the effects of hyperbaric oxygen (HBO) on mouse skin carcinogenesis induced by 7,12-dimethylbenz[a]anthracene (DMBA) and 12-O-tetradecanoylphorbol-13-acetate (TPA).
Main Methods:
- Six-week-old female CD-1 mice were divided into normoxia and HBO groups.
- Carcinogenesis was induced using DMBA as an initiator and TPA as a promoter.
- Tumor incidence, grade, and Ki-67 labeling index were assessed over 23 weeks.
Main Results:
- Mice exposed to HBO developed tumors earlier and exhibited a higher proportion of high-grade papillomas and squamous cell carcinomas (SCCs).
- Ki-67 labeling indices were significantly higher in low-grade papillomas from the HBO group (29.67%) compared to the normoxia group (15.27%).
- HBO treatment accelerated tumor cell proliferation and advanced tumor progression.
Conclusions:
- Hyperbaric oxygen therapy accelerated tumor cell proliferation and advanced tumor progression in a mouse model of skin carcinogenesis.
- These findings suggest that HBO may promote skin cancer development and progression.
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