Parameters of Protection Against Ultraviolet Radiation-induced Skin Cell Damage

被引:39
作者
Cao, Cong [1 ]
Wan, Yinsheng [2 ]
机构
[1] Brown Univ, Dept Mol Microbiol & Immunol, Pathobiol Program, Providence, RI 02912 USA
[2] Providence Coll, Dept Biol, Providence, RI 02918 USA
关键词
ACTIVATED PROTEIN-KINASE; MAMMALIAN TARGET; GROWTH-FACTOR; IN-VIVO; TRANSLATIONAL CONTROL; SIGNALING PATHWAY; MTOR; P53; PHOSPHORYLATION; UV;
D O I
10.1002/jcp.21780
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Epidemiological and experimental evidence has supported the notion that solar ultraviolet (UV) radiation is the leading cause of skin cell damage and skin cancer. Non-melanoma skin cancer, one of the malignancies with the most rapidly increasing incidence, is suggested to be directly related to the total exposure to solar UV light. Over the past few years, the mechanisms of cellular responses to UV radiation have received unprecedented attention. Understanding how skin cells respond to UV radiation will undoubtedly help decipher what goes wrong in a variety of clinical skin disorders including skin cancer and will facilitate the development of novel therapeutic strategies. In the past decade, studies have established that UV radiation induces multifarious signal transcluction pathways, some of which lead to apoptotic cell death, while others protect against this process. In this review, we summarize some of the most recent progresses regarding the involvement of multiple signal pathways in UV radiation-induced apoptosis in skin cells, especially in keratinocytes. These pathways include pro-apoptosis components such as MAPK, AMPK, and p53 as well as pro-survival components, namely, AKT and mTORC complexes. J. Cell. Physiol. 220: 277-284, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:277 / 284
页数:8
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