Dixon Katie M, Tongkao-On Wannit, Sequeira Vanessa B, Carter Sally E, Song Eric J, Rybchyn Mark S, Gordon-Thomson Clare, Mason Rebecca S
Discipline of Physiology, Bosch Institute, School of Medical Sciences, University of Sydney, Sydney, NSW 2006, Australia.
Int J Mol Sci. 2013 Jan 18;14(1):1964-77. doi: 10.3390/ijms14011964.
Exposure to sunlight is the major cause of skin cancer. Ultraviolet radiation (UV) from the sun causes damage to DNA by direct absorption and can cause skin cell death. UV also causes production of reactive oxygen species that may interact with DNA to indirectly cause oxidative DNA damage. UV increases accumulation of p53 in skin cells, which upregulates repair genes but promotes death of irreparably damaged cells. A benefit of sunlight is vitamin D, which is formed following exposure of 7-dehydrocholesterol in skin cells to UV. The relatively inert vitamin D is metabolized to various biologically active compounds, including 1,25-dihydroxyvitamin D3. Therapeutic use of vitamin D compounds has proven beneficial in several cancer types, but more recently these compounds have been shown to prevent UV-induced cell death and DNA damage in human skin cells. Here, we discuss the effects of vitamin D compounds in skin cells that have been exposed to UV. Specifically, we examine the various signaling pathways involved in the vitamin D-induced protection of skin cells from UV.
暴露于阳光下是皮肤癌的主要成因。来自太阳的紫外线(UV)通过直接吸收对DNA造成损伤,并可导致皮肤细胞死亡。UV还会引发活性氧的产生,活性氧可能与DNA相互作用,间接导致氧化性DNA损伤。UV会增加皮肤细胞中p53的积累,这会上调修复基因,但会促使无法修复的受损细胞死亡。阳光的一个益处是维生素D,它是皮肤细胞中的7-脱氢胆固醇暴露于UV后形成的。相对惰性的维生素D会代谢为多种生物活性化合物,包括1,25-二羟基维生素D3。维生素D化合物的治疗用途已在多种癌症类型中被证明有益,但最近这些化合物已被证明可预防UV诱导的人类皮肤细胞死亡和DNA损伤。在此,我们讨论维生素D化合物在暴露于UV的皮肤细胞中的作用。具体而言,我们研究了维生素D诱导的保护皮肤细胞免受UV影响所涉及的各种信号通路。