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MicroRNAs in Nonalcoholic Fatty Liver Disease

机译:非酒精性脂肪肝疾病中的MicroRNA

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摘要

Nonalcoholic fatty liver disease (NAFLD) has become the most common liver disorder. Strongly linked to obesity and diabetes, NAFLD has the characteristics of complex diseases with substantial heterogeneity. Accordingly, our ability to predict the risk of advanced NAFLD and provide efficient treatment may improve by a better understanding of the relationship between genotype and phenotype. MicroRNAs (miRNAs) play a major role in the fine-tuning of gene expression and they have recently emerged as novel biomarkers and therapeutic tools in the management of NAFLD. These short non-coding RNA sequences act by partial repression or degradation of targeted mRNAs. Deregulation of miRNAs has been associated with different stages of NAFLD, while their biological role in the pathogenesis remains to be fully understood. Systems biology analyses based on predicted target genes have associated hepatic miRNAs with molecular pathways involved in NAFLD progression such as cholesterol and lipid metabolism, insulin signaling, oxidative stress, inflammation, and pathways of cell survival and proliferation. Moreover, circulating miRNAs have been identified as promising noninvasive biomarkers of NAFLD and linked to disease severity. This rapidly growing field is likely to result in major advances in the pathomechanism, prognostication, and treatment of NAFLD.
机译:非酒精性脂肪性肝病(NAFLD)已成为最常见的肝病。 NAFLD与肥胖和糖尿病密切相关,具有复杂的疾病特征,具有很大的异质性。因此,通过更好地了解基因型和表型之间的关系,我们预测晚期NAFLD风险和提供有效治疗的能力可能会提高。 MicroRNA(miRNA)在基因表达的微调中起着重要作用,最近它们已成为NAFLD管理中的新型生物标志物和治疗工具。这些短的非编码RNA序列通过部分抑制或降解靶mRNA发挥作用。 miRNA的失调与NAFLD的不同阶段有关,而其在发病机理中的生物学作用尚待充分了解。基于预测目标基因的系统生物学分析已将肝miRNA与参与NAFLD进展的分子途径相关联,例如胆固醇和脂质代谢,胰岛素信号传导,氧化应激,炎症以及细胞存活和增殖的途径。此外,循环中的miRNA已被鉴定为有前途的NAFLD生物标记物,并与疾病的严重程度相关。这个快速增长的领域可能会导致NAFLD的发病机制,预后和治疗方面取得重大进展。

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