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常染色体隐性先天性鱼鳞病的最新进展:利用毛发样本进行mRNA分析是基因诊断的有力工具。

Update on autosomal recessive congenital ichthyosis: mRNA analysis using hair samples is a powerful tool for genetic diagnosis.

作者信息

Sugiura Kazumitsu, Akiyama Masashi

机构信息

Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

出版信息

J Dermatol Sci. 2015 Jul;79(1):4-9. doi: 10.1016/j.jdermsci.2015.04.009. Epub 2015 Apr 30.

Abstract

Research on the molecular genetics and pathomechanisms of autosomal recessive congenital ichthyosis (ARCI) has advanced considerably and several causative genes and molecules underlying the disease have been identified. Three major ARCI phenotypes are harlequin ichthyosis (HI), lamellar ichthyosis (LI), and congenital ichthyosiform erythroderma (CIE). Skin barrier defects are involved in the pathogenesis of ARCI. In this review, the causative genes of ARCI and its phenotypes as well as recent advances in the field are summarized. The known causative molecules underlying ARCI include ABCA12, TGM1, ALOXE3, ALOX12B, NIPAL4, CYP4F22, PNPLA1, CERS3, and LIPN. It is important to examine genetic associations and to elucidate the pathomechanisms of ARCI to establish effective therapies and beneficial genetic counseling. Next-generation sequencing is a promising method that enables the detection of causative disease mutations, even in cases of unexpected concomitant genetic diseases. For genetic diagnosis, obtaining mRNA from hair follicle epithelial cells, which are analogous to keratinocytes in the interfollicular epidermis, is convenient and minimally invasive in patients with ARCI. We confirmed that our mRNA analysis method using hair follicle samples can be applied not only to keratinization disorders, but also to other genetic diseases in the dermatology field. Studies that suggest potential next-generation therapies using ARCI model mice are also reviewed.

摘要

常染色体隐性先天性鱼鳞病(ARCI)的分子遗传学和发病机制研究取得了显著进展,已鉴定出该疾病的几个致病基因和相关分子。ARCI有三种主要表型,即丑角样鱼鳞病(HI)、板层状鱼鳞病(LI)和先天性鱼鳞病样红皮病(CIE)。皮肤屏障缺陷参与了ARCI的发病机制。在这篇综述中,总结了ARCI及其表型的致病基因以及该领域的最新进展。已知的ARCI致病分子包括ABCA12、TGM1、ALOXE3、ALOX12B、NIPAL4、CYP4F22、PNPLA1、CERS3和LIPN。研究基因关联并阐明ARCI的发病机制对于建立有效的治疗方法和提供有益的遗传咨询非常重要。新一代测序是一种很有前景的方法,即使在存在意外并发遗传病的情况下,也能够检测致病疾病突变。对于基因诊断,从毛囊上皮细胞获取mRNA很方便,毛囊上皮细胞类似于毛囊间表皮中的角质形成细胞,对ARCI患者的侵入性最小。我们证实,我们使用毛囊样本的mRNA分析方法不仅可以应用于角化障碍,还可以应用于皮肤科领域的其他遗传病。本文还综述了使用ARCI模型小鼠进行潜在新一代治疗方法的研究。

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