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紫外线诱导的黑色素化学激发:黑色素瘤发病机制的新模式。

UV-induced Melanin Chemiexcitation: A New Mode of Melanoma Pathogenesis.

作者信息

Brash Douglas E

机构信息

Department of Therapeutic Radiology, Yale School of Medicine, New Haven, Connecticut, USA

出版信息

Toxicol Pathol. 2016 Jun;44(4):552-4. doi: 10.1177/0192623316632072. Epub 2016 Mar 7.

Abstract

Mutations in sunlight-induced melanoma arise from cyclobutane pyrimidine dimers (CPDs), DNA photoproducts usually created picoseconds after an ultraviolet (UV) photon is absorbed at thymine or cytosine. Surprisingly, we found that, in melanocytes, CPDs were generated for hours after UVA or UVB exposure. These "dark CPDs" constituted the majority of CPDs in cultured human and murine melanocytes and in mouse skin, and they were most prominent in skin containing pheomelanin, the melanin responsible for blonde and red hair. The mechanism was also a surprise. Dark cyclobutane pyrimidine dimers (CPDs) arise when ultraviolet (UV)-induced superoxide and nitric oxide combine to form peroxynitrite, one of the few biological molecules capable of exciting an electron. This process, termed "chemiexcitation," is the source of bioluminescence in lower organisms. Excitation occurred in fragments of melanin, creating a quantum triplet state that had the energy of a UV photon but which induced CPDs by radiationless energy transfer to DNA. UVA and peroxynitrite also solubilized melanin and permeabilized the nuclear membrane, allowing melanin to enter. Melanin is evidently carcinogenic as well as protective. Chemiexcitation may also trigger pathogenesis in internal tissues because the same chemistry should arise wherever superoxide and nitric oxide arise near cells that contain melanin.

摘要

阳光诱导的黑色素瘤中的突变源于环丁烷嘧啶二聚体(CPD),这是一种DNA光产物,通常在紫外线(UV)光子被胸腺嘧啶或胞嘧啶吸收后的皮秒内形成。令人惊讶的是,我们发现,在黑素细胞中,UVA或UVB照射后数小时都会产生CPD。这些“暗CPD”在培养的人类和小鼠黑素细胞以及小鼠皮肤中构成了CPD的大部分,并且在含有褐黑素(负责金色和红色头发的黑色素)的皮肤中最为突出。其机制同样令人惊讶。当紫外线诱导的超氧化物和一氧化氮结合形成过氧亚硝酸盐时,就会产生暗环丁烷嘧啶二聚体(CPD),过氧亚硝酸盐是少数能够激发电子的生物分子之一。这个过程被称为“化学激发”,是低等生物生物发光的来源。激发发生在黑色素片段中,产生一个具有紫外线光子能量的量子三重态,但它通过无辐射能量转移到DNA来诱导CPD。UVA和过氧亚硝酸盐还能溶解黑色素并使核膜通透性增加,从而使黑色素进入。黑色素显然既有致癌性又有保护作用。化学激发也可能触发内部组织的发病机制,因为只要超氧化物和一氧化氮在含有黑色素的细胞附近产生,就会发生同样的化学反应。

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