Abstract

Germicidal lamps that emit primarily 254 nm ultraviolet radiation (UV) are routinely utilized for surface sterilization but cannot be used for human skin because they cause genotoxicity. As an alternative, 222‐nm UVC has been reported to exert sterilizing ability comparable to that of 254‐nm UVC without producing cyclobutane pyrimidine dimers (CPDs), the major DNA lesions caused by UV. However, there has been no clear evidence for safety in chronic exposure to skin, particularly with respect to carcinogenesis. We therefore investigated the long‐term effects of 222‐nm UVC on skin using a highly photocarcinogenic phenotype mice that lack xeroderma pigmentosum complementation group A (Xpa‐) gene, which is involved in repairing of CPDs. CPDs formation was recognized only uppermost layer of epidermis even with high dose of 222‐nm UVC exposure. No tumors were observed in Xpa‐knockout mice and wild‐type mice by repetitive irradiation with 222‐nm UVC, using a protocol which had shown to produce tumor in Xpa‐knockout mice irradiated with broad‐band UVB. Furthermore, erythema and ear swelling were not observed in both genotype mice following 222‐nm UVC exposure. Our data suggest that 222‐nm UVC lamps can be safely used for sterilizing human skin as far as the perspective of skin cancer development.

Highlights

  • Ultraviolet radiation C (UVC) is defined as 100–280 nm wavelengths UV

  • The 222-nm UVC lamp is designated as irradiator A. [Correction added on July 08, 2020, after first online publication: The figure was updated.]

  • Our results indicated that long-term irradiation of mice with 222nm UVC failed to induce nonmelanoma skin tumors, even in

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Summary

Introduction

Ultraviolet radiation C (UVC) is defined as 100–280 nm wavelengths UV. Germicidal lamps that primarily emit 254-nm UVC have been utilized for sterilization because this wavelength is effective for killing bacteria. In spite of the usefulness of 254-nm UVC lamps for sterilization, it is well known to be harmful to skin and eyes, causing erythema and keratitis, respectively. License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. Xpa-knockout mice are extremely hypersensitive to UV and highly susceptible to UV-induced skin carcinogenesis [19,20,21,22]

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