Powers Julia Montelin, Murphy Gillian, Ralph Nikki, O'Gorman Susan M, Murphy James E J
Mitochondrial Biology & Radiation Research Centre, Dept Life Sciences, IT Sligo, Sligo, Ireland.
Dept of Dermatology, Beaumont Hospital, Dublin, Ireland.
J Photochem Photobiol B. 2017 Aug;173:397-403. doi: 10.1016/j.jphotobiol.2017.06.020. Epub 2017 Jun 17.
Most somatic cells contain many copies of mitochondrial DNA (mtDNA). Because of both the high copy number and the lack of repair mechanisms available to mtDNA, damage to it largely goes unrepaired, and can accumulate over time. Large scale deletions are a recognised type of damage sustained by mtDNA as a consequence of exposure to the ultraviolet light in sunlight. A group of patients were identified as having abnormally high levels of either a 4977 base pair deletion (mtDNA) or 3895 base pair deletion (mtDNA), in mtDNA from sun exposed skin or skin suspected to be a non-melanoma skin cancer, but not in their non-sun exposed skin biopsies. In three of the four cases, skin cancer was ruled out due to histological testing. Additional factors from these patients' medical histories were studied, and it was noted that they shared diagnoses for multiple pathologies common to an older population, and that they were being treated with the same or related pharmaceuticals, including some that had been known to cause dermal side effects. Investigation into the biochemistry underlying the symptoms, the effects of sun exposure and side effects of the prescribed pharmaceuticals revealed a possible synergistic relationship leading to the localised high levels of mtDNA deletions.
大多数体细胞含有许多拷贝的线粒体DNA(mtDNA)。由于mtDNA的拷贝数高且缺乏可用的修复机制,其损伤大多未得到修复,并会随着时间积累。大规模缺失是mtDNA因暴露于阳光中的紫外线而遭受的一种公认的损伤类型。一组患者被确定为在暴露于阳光的皮肤或疑似非黑色素瘤皮肤癌的皮肤的mtDNA中,4977碱基对缺失(mtDNA)或3895碱基对缺失(mtDNA)的水平异常高,但在其未暴露于阳光的皮肤活检组织中则没有。在这四个病例中的三个中,经组织学检测排除了皮肤癌。对这些患者病史中的其他因素进行了研究,发现他们都患有老年人群常见的多种疾病,并且正在接受相同或相关的药物治疗,其中一些药物已知会引起皮肤副作用。对症状背后的生物化学、阳光暴露的影响以及处方药物的副作用进行调查后发现,可能存在协同关系导致mtDNA局部高水平缺失。