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类风湿关节炎中新兴的表观遗传学靶点。

Emerging epigenetic targets in rheumatoid arthritis.

机构信息

Department of Pharmacology, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Vile Parle (West), Mumbai, 400056, India.

出版信息

Rheumatol Int. 2021 Dec;41(12):2047-2067. doi: 10.1007/s00296-021-04951-y. Epub 2021 Jul 26.

Abstract

Rheumatoid arthritis is a complex disorder that is characterized by irreversible and progressive destructions of joints, but its exact etiology remains mainly unknown. The occurrence and the progression of the disease entirely depend on environmental and genetic factors. In recent years, various epigenetic changes involving DNA methylation, histone modification, miRNA, X-chromosome inactivation, bromodomain, sirtuin, and many others were identified that were found to be linked to the activation and the aggressive phenotype in rheumatoid arthritis. Epigenetics is found to be one of the root causes, which brings changes in the heritable phenotype and is not determined by changes in the DNA sequences and understanding these epigenetic mechanisms and the pathogenesis of the disease can help in understanding the disease and various other possible ways for its control and/or prevention. The various epigenetic modification occurring are reversible and can be modulated by drugs, diet, and environmental factors. This article focuses on various epigenetic factors involved in the pathogenesis of rheumatoid arthritis. Further, various epigenetic therapies that might be successful in inhibiting these epigenetic modifications are summarized. Several therapeutic agents alter the epigenetic modifications occurring in various diseases and many of the epigenetic therapies are under pre-clinical and clinical trial. However, exploring these epigenetic prognostic biomarkers would give a broader perspective and provide more ideas and knowledge regarding the process and pathways through which the diseases occur, and also combining various therapeutic agents would show more beneficial and synergistic effects.

摘要

类风湿关节炎是一种复杂的疾病,其特征为关节的不可逆转和进行性破坏,但确切的病因主要仍不清楚。疾病的发生和进展完全取决于环境和遗传因素。近年来,已确定涉及 DNA 甲基化、组蛋白修饰、miRNA、X 染色体失活、溴结构域、沉默调节蛋白、许多其他因素的各种表观遗传变化与类风湿关节炎的激活和侵袭表型有关。表观遗传学被认为是其中的一个根本原因,它会导致可遗传表型的变化,而不是由 DNA 序列的变化决定,了解这些表观遗传机制和疾病的发病机制有助于理解疾病以及控制和/或预防疾病的各种其他可能途径。发生的各种表观遗传修饰是可逆的,可以通过药物、饮食和环境因素进行调节。本文重点介绍了参与类风湿关节炎发病机制的各种表观遗传因素。此外,还总结了可能成功抑制这些表观遗传修饰的各种表观遗传治疗方法。几种治疗剂改变了各种疾病中发生的表观遗传修饰,许多表观遗传治疗方法正在进行临床前和临床试验。然而,探索这些表观遗传预后生物标志物将提供更广泛的视角,并提供更多关于疾病发生过程和途径的想法和知识,同时结合各种治疗剂将显示出更有益和协同的效果。

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