吡格列酮是治疗共济失调-特朗吉特氏病的一种可能方法。

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2024-10-08 DOI:10.3390/biom14101264
Rodney Shackelford
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引用次数: 0

摘要

共济失调性小脑共济失调症(AT)是一种罕见的常染色体隐性遗传疾病,以免疫缺陷、进行性小脑共济失调和恶性肿瘤风险增加为特征。从 AT 患者身上提取的细胞显示出多种缺陷,包括对氧化剂和电离辐射的敏感性高、DNA 修复能力差、铁硫簇水平低和还原型谷胱甘肽含量低。AT 的临床病程是渐进的、无休止的,大多数患者的存活时间约为 25 年。目前,AT 还没有有效的治疗方法,大多数患者只能接受支持性治疗。最近,用于治疗 2 型糖尿病的噻唑烷二酮类药物吡格列酮已被证明对 AT 细胞和患有 AT 的糖尿病患者有益。在这里,我将讨论吡格列酮对AT表型产生有利影响的可能分子机制,以及为什么它在治疗AT的某些方面可能有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pioglitazone as a Possible Treatment for Ataxia-Telangiectasia.

Ataxia-telangiectasia (AT) is a rare autosomal recessive disorder characterized by immunodeficiency, progressive cerebellar ataxia, and an increased malignancy risk. Cells derived from individuals with AT show multiple defects, including high oxidant and ionizing radiation sensitivities, poor DNA repair, low iron-sulfur cluster levels, and low reduced glutathione. The clinical course of AT is progressive and unrelenting, with most individuals having a survival time of approximately twenty-five years. Presently, AT has no effective treatments, and most patients receive supportive care only. Recently, pioglitazone, a thiazolidinedione class used to treat type 2 diabetes, has been demonstrated to exert beneficial effects on AT cells and on diabetic individuals with AT. Here, I will discuss the possible molecular mechanisms of pioglitazone's favorable effects on the AT phenotype and why it may have utility in treating some aspects of AT.

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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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