Abstract

Narrow band ultraviolet B (NB-UVB) and Broad band ultraviolet B (BB-UVB) are commonly used for the treatment of Atopic Dermatitis (AD) among others, and has been shown by us and others to trigger LINE-1 reactivation in human keratinocytes. LINE-1 constitutes ∼17% of human genome, has played important evolutionary role, and its reactivation may result in deleterious effects leading to DNA damage, cellular senescence and photoaging. We established a model of NB-UVB or BB-UVB irradiation on keratinocytes, and showed that these induced an increase in LINE-1 expression.

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