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紫外线诱导的DNA损伤修复缺陷的遗传性疾病。

Hereditary Disorders with Defective Repair of UV-Induced DNA Damage.

作者信息

Moriwaki Shinichi

机构信息

Department of Dermatology, Osaka Medical College, Takatsuki, Japan.

出版信息

Jpn Clin Med. 2013 Apr 16;4:29-35. doi: 10.4137/JCM.S10730. eCollection 2013.

Abstract

Nucleotide excision repair (NER) is an essential system for correcting ultraviolet (UV)-induced DNA damage. Lesions remaining in DNA due to reduced capacity of NER may result in cellular death, premature aging, mutagenesis and carcinogenesis of the skin. So, NER is an important protection against these changes. There are three representative genodermatoses resulting from genetic defects in NER: xeroderma pigmentosum (XP), Cockayne syndrome (CS), and trichothiodystrophy (TTD). In Japan, CS is similarly rare but XP is more common and TTD is less common compared to Western countries. In 1998, we established the system for the diagnosis of these disorders and we have been performing DNA repair and genetic analysis for more than 400 samples since then. At present, there is no cure for any human genetic disorder. Early diagnosis and symptomatic treatment of neurological, ocular and dermatological abnormalities should contribute to prolonging life and elevating QOL in patients.

摘要

核苷酸切除修复(NER)是纠正紫外线(UV)诱导的DNA损伤的重要系统。由于NER能力降低而残留在DNA中的损伤可能导致细胞死亡、早衰、诱变和皮肤癌变。因此,NER是防止这些变化的重要保护机制。有三种由NER基因缺陷引起的代表性遗传性皮肤病:着色性干皮病(XP)、科凯恩综合征(CS)和毛发硫营养不良(TTD)。在日本,CS同样罕见,但与西方国家相比,XP更为常见,TTD则较少见。1998年,我们建立了这些疾病的诊断系统,从那时起,我们已经对400多个样本进行了DNA修复和基因分析。目前,尚无治疗任何人类遗传疾病的方法。对神经、眼睛和皮肤异常进行早期诊断和对症治疗应有助于延长患者寿命并提高其生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe68/3742358/d235ddee3b58/jcm-4-2013-029f1.jpg

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