Effect of immunosuppressive agents and sunscreens on UV carcinogenesis in the hairless mouse
- PMID: 3879583
- DOI: 10.1038/icb.1985.69
Effect of immunosuppressive agents and sunscreens on UV carcinogenesis in the hairless mouse
Abstract
The effect of two immunosuppressive agents, azathioprine and cyclophosphamide, with and without UVB sunscreen protection on UV-induced skin carcinogenesis was studied in the albino hairless mouse. In a daily treatment regime spanning 9 weeks, groups of mice were immunosuppressed with either drug, and were exposed to minimally erythemal doses of a light source simulating the UV portion of the solar spectrum. The accumulated UV exposure alone induced skin tumours in 77% of mice. Azathioprine, but not cyclophosphamide, significantly enhanced the incidence of UV tumorigenesis. Photoprotection by topical application of one of two commonly used UVB sunscreens, 2-ethyl-hexyl-p-methoxycinnamate (2-EHMC) or octyl-N-dimethyl-p-aminobenzoate (o-PABA), reduced the UV tumour incidence to zero in immunologically normal mice and to 8-15% in immunosuppressed mice. Unexpressed latent tumour initiations were revealed in all sunscreen-protected groups by the subsequent application of a tumour promoter, croton oil. In immunologically normal mice 2-EHMC had allowed initiations in 39% of UV-irradiated mice, and o-PABA in 16.5%. However, in UV-irradiated mice immunosuppressed with azathioprine there had been initiations in 78% of mice protected with 2-EHMC and 65% of mice protected with o-PABA. Photoprotected mice immunosuppressed with cyclophosphamide did not show the same increase in UV-initiations (22% with 2-EHMC, 23% with o-PABA). These results provide evidence that azathioprine increases the susceptibility of the skin to UV carcinogenesis. However, UVB sunscreens afford effective protection from overt tumour expression in the absence of a tumour promoter.
Similar articles
-
Differential protection by two sunscreens from UV radiation-induced immunosuppression.J Invest Dermatol. 1991 Oct;97(4):624-8. doi: 10.1111/1523-1747.ep12483006. J Invest Dermatol. 1991. PMID: 1940432
-
Ultraviolet carcinogenesis in the hairless mouse skin. Influence of the sunscreen 2-ethylhexyl-p-methoxycinnamate.Aust J Exp Biol Med Sci. 1984 Oct;62 ( Pt 5):577-88. doi: 10.1038/icb.1984.55. Aust J Exp Biol Med Sci. 1984. PMID: 6534345
-
Interaction of UVB-absorbing sunscreen ingredients with cutaneous molecules may alter photoimmune protection.Photochem Photobiol. 2001 Dec;74(6):765-70. doi: 10.1562/0031-8655(2001)0742.0.co;2. Photochem Photobiol. 2001. PMID: 11783931
-
Broad-spectrum sunscreens provide better protection from solar ultraviolet-simulated radiation and natural sunlight-induced immunosuppression in human beings.J Am Acad Dermatol. 2008 May;58(5 Suppl 2):S149-54. doi: 10.1016/j.jaad.2007.04.035. J Am Acad Dermatol. 2008. PMID: 18410801 Review.
-
Sunscreens.Adv Exp Med Biol. 2014;810:429-63. doi: 10.1007/978-1-4939-0437-2_25. Adv Exp Med Biol. 2014. PMID: 25207381 Review.
Cited by
-
Topical and oral retinoids protect Langerhans' cells and epidermal Thy-1+ dendritic cells from being depleted by ultraviolet radiation.Immunology. 1991 Nov;74(3):425-31. Immunology. 1991. PMID: 1685145 Free PMC article.
-
Estrogen receptor signaling protects against immune suppression by UV radiation exposure.Proc Natl Acad Sci U S A. 2006 Aug 22;103(34):12837-42. doi: 10.1073/pnas.0603642103. Epub 2006 Aug 14. Proc Natl Acad Sci U S A. 2006. PMID: 16908847 Free PMC article.
-
Chemoprevention of ultraviolet radiation-induced skin cancer.Environ Health Perspect. 1997 Jun;105 Suppl 4(Suppl 4):981-4. doi: 10.1289/ehp.97105s4981. Environ Health Perspect. 1997. PMID: 9255591 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical