紫外线诱导突变与皮肤癌的机制。

Genome instability & disease Pub Date : 2020-05-01 Epub Date: 2020-03-19 DOI:10.1007/s42764-020-00009-8
Gerd P Pfeifer
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引用次数: 44

摘要

紫外线(UV)照射引起各种类型的DNA损伤,从而导致特定的突变和人类皮肤癌的出现,通常在初次暴露后几十年。不同的紫外线波长导致形成明显的紫外线诱导的DNA损伤。大多数这些病变是由核苷酸切除修复途径,这是有缺陷的罕见遗传性皮肤病,称为色素性干皮病。环丁烷嘧啶二聚体(CPDs)在诱导阳光依赖性皮肤癌突变中起主要作用。本文综述了紫外线损伤诱导的机制、损伤的基因组分布、相关的DNA修复机制、紫外线诱导CPDs在哺乳动物细胞中产生DNA复制依赖性诱变的可能机制,以及在皮肤癌基因组中发现的紫外线损伤和诱变的强特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanisms of UV-induced mutations and skin cancer.

Mechanisms of UV-induced mutations and skin cancer.

Mechanisms of UV-induced mutations and skin cancer.

Mechanisms of UV-induced mutations and skin cancer.

Ultraviolet (UV) irradiation causes various types of DNA damage, which leads to specific mutations and the emergence of skin cancer in humans, often decades after initial exposure. Different UV wavelengths cause the formation of prominent UV-induced DNA lesions. Most of these lesions are removed by the nucleotide excision repair pathway, which is defective in rare genetic skin disorders referred to as xeroderma pigmentosum. A major role in inducing sunlight-dependent skin cancer mutations is assigned to the cyclobutane pyrimidine dimers (CPDs). In this review, we discuss the mechanisms of UV damage induction, the genomic distribution of this damage, relevant DNA repair mechanisms, the proposed mechanisms of how UV-induced CPDs bring about DNA replication-dependent mutagenicity in mammalian cells, and the strong signature of UV damage and mutagenesis found in skin cancer genomes.

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