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UVA 光解 DNA 6-硫代鸟嘌呤导致的多种形式的 DNA 损伤。

Multiple forms of DNA damage caused by UVA photoactivation of DNA 6-thioguanine.

机构信息

Cancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.

出版信息

Photochem Photobiol. 2012 Jan-Feb;88(1):5-13. doi: 10.1111/j.1751-1097.2011.01043.x. Epub 2011 Dec 16.

Abstract

Thiopurines are prescribed frequently as medication for cancer and for inflammatory disorders. One of them, azathioprine, has been the immunosuppressant of choice for organ transplant recipients for many years. Thiopurine use is associated with elevated sun sensitivity and skin cancer risk. Skin sensitization is selective for UVA. 6-TG integrates into DNA and unlike the canonical DNA bases, it is a strong UVA chromophore with an absorbance maximum at 342 nm. DNA 6-TG is a photosensitizer and a source of reactive oxygen species. Reactive oxygen that is generated from the photochemical activation of DNA 6-TG causes extensive damage to DNA and proteins. This damage is mutagenic and extremely toxic to cultured human cells. Here we describe some of the lesions that are known to be generated from UVA irradiation of DNA 6-TG. We discuss how this photochemical damage might contribute to the toxic effect of thiopurine/UVA treatment on cultured cells and to the high risk of skin cancer in thiopurine-treated patients.

摘要

硫嘌呤类药物经常被开为癌症和炎症性疾病的药物。其中一种,巯嘌呤,多年来一直是器官移植受者的首选免疫抑制剂。硫嘌呤类药物的使用与日晒敏感性和皮肤癌风险增加有关。皮肤致敏作用是选择性的 UVA。6-TG 整合到 DNA 中,与典型的 DNA 碱基不同,它是一种强 UVA 发色团,最大吸收波长在 342nm。DNA 6-TG 是一种光敏剂和活性氧的来源。来自 DNA 6-TG 的光化学激活产生的活性氧会对 DNA 和蛋白质造成广泛的损伤。这种损伤具有致突变性,对培养的人类细胞具有极高的毒性。在这里,我们描述了已知由 UVA 照射 DNA 6-TG 产生的一些损伤。我们讨论了这种光化学损伤如何导致硫嘌呤/ UVA 处理对培养细胞的毒性作用,以及硫嘌呤治疗患者皮肤癌风险高的原因。

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