小眼畸形相关转录因子
黄褐斑
黑色素
色素沉着
皮肤癌
黑素细胞
黑素皮质素1受体
人体皮肤
皮肤病科
酪氨酸酶
皮肤色素沉着
表皮(动物学)
深色皮肤
紫外线辐射
色素沉着障碍
医学
光老化
表型
生物
化学
癌症研究
黑色素瘤
癌症
内科学
生物化学
酶
解剖
遗传学
放射化学
基因
作者
Inbal Rachmin,Stephen M. Ostrowski,Qing Yu Weng,David E. Fisher
标识
DOI:10.1016/j.addr.2020.02.002
摘要
Skin pigmentation is a result of melanin produced by melanocytes in the epidermis. Melanocyte activity, along with the type and distribution of melanins, is the main driver for diversity of skin pigmentation. Dark melanin acts to protect against the deleterious effects of ultraviolet (UV) radiation, including photo-aging and skin cancer formation. In turn, UV radiation activates skin melanocytes to induce further pigmentation (i.e., "tanning pathway"). The well-characterized MSH/MC1R-cAMP-MITF pathway regulates UV-induced melanization. Pharmacologic activation of this pathway ("sunless tanning") represents a potential strategy for skin cancer prevention, particularly in those with light skin or the "red hair" phenotype who tan poorly after UV exposure due to MC1R inactivating polymorphisms. Skin hyperpigmentation can also occur as a result of inflammatory processes and dermatological disorders such as melasma. While primarily of cosmetic concern, these conditions can dramatically impact quality of life of affected patients. Several topical agents are utilized to treat skin pigmentation disorders. Here, we review melanogenesis induced by UV exposure and the agents that target this pathway.
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