Neonatal mice do not have increased sensitivity to induction of squamous cell carcinomas

Authors


  • Conflicts of interest:

    None.

Correspondence:

Dr Catharina M. Lerche, PhD, Department of Dermatology, Copenhagen University Hospital, Bispebjerg, D92, Bispebjerg Bakke 23, DK-2400 Copenhagen NV, Denmark.

Tel: +45 35312778

Fax: +45 35316010

e-mail: cler0001@bbh.regionh.dk

Summary

Background

Squamous cell carcinoma (SCC) is linked with the lifelong cumulative effect of ultraviolet radiation (UVR). In contrast, epidemiological data have shown that sunburn in childhood is a stronger risk factor for cutaneous malignant melanoma than continuous UVR, indicating a higher carcinogenic sensitivity early in life.

Methods

We investigated how a high neonatal dose of UVR affects the development of SCC in mice irradiated later in life. We used simulated solar radiation (sun) and solarium radiation (solarium). Ninety-nine C3.Cg/TifBomTac-immunocompetent hairless mice received 0, 25 or 35 standard erythema doses (SED) UVR when they were 4 days old followed by 4 SED sun or 4 SED solarium three times/weekly from 9 weeks of age.

Results

Tumours developed faster in mice treated with 35 SED UVR + 4 SED sun compared with 4 SED sun, but no change was observed in the cumulative dose required to achieve tumours. Tumours also developed faster in mice treated with 35 SED UVR + 4 SED solarium compared with 4 SED solarium, and a difference was also observed in the cumulative dose required to achieve tumours. If the Skin Cancer Utrecht-Philadelphia-murine spectrum was used to weigh the delivered irradiance instead of the International Commission on Illumination erythema action spectrum, tumours developed after the same accumulated dose.

Conclusion

In conclusion, this study does not indicate increased sensitivity to induction of SCC early in life.

Ancillary