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Rheumatoid Arthritis and miRNAs: A Critical Review through a Functional View

机译:类风湿关节炎和miRNA:通过功能观点的批判性审查

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Rheumatoid arthritis (RA) is a systemic autoimmune disease with severe joint inflammation and destruction associated with an inflammatory environment. The etiology behind RA remains to be elucidated; most updated concepts include the participation of environmental, proteomic, epigenetic, and genetic factors. Epigenetic is considered the missing link to explain genetic diversification among RA patients. Within epigenetic factors participating in RA, miRNAs are defined as small noncoding molecules with a length of approximately 22 nucleotides, capable of gene expression modulation, either negatively through inhibition of translation and degradation of the mRNA or positively through increasing the translation rate. Over the last decade and due to the feasibility of the identification of miRNAs among different tissues and compartments, they have been proposed as biomarkers for diagnosis, prognosis, and response to treatment in different pathologies. Nevertheless, miRNAs seem to be important regulators of networks instead of single genes; their hypothetical use as biomarkers needs to rely on a functional integrative description of their effects in the biological process of autoimmune conditions which until now is missing. Therefore, we underwent a bibliographic search for review and original articles related to miRNAs and their possible implications in rheumatoid arthritis. We found 48 different studies using the
机译:类风湿关节炎(RA)是一种全身性自身免疫性疾病,具有严重的关节发炎和与发炎环境相关的破坏。 RA的病因有待阐明。最新的概念包括环境,蛋白质组,表观遗传和遗传因素的参与。表观遗传被认为是解释RA患者遗传多样性的缺失环节。在参与RA的表观遗传因子中,miRNA被定义为小的非编码分子,其长度约为22个核苷酸,能够通过抑制mRNA的翻译和降解来产生负调控,或者通过提高翻译速率来发挥正调控基因表达的能力。在过去的十年中,由于在不同组织和隔室之间鉴定miRNA的可行性,已提出将它们作为诊断,预后和对不同病理学治疗反应的生物标志物。然而,miRNA似乎是网络的重要调节剂,而不是单个基因。它们作为生物标志物的假设用途需要依靠功能综合描述其在自身免疫性疾病的生物学过程中所起的作用,而该过程至今仍不存在。因此,我们进行了书目搜索,以查找有关miRNA及其在类风湿关节炎中的潜在影响的评论和原始文章。我们发现48种不同的研究使用了

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