肠缺血再灌注损伤中的细胞外基质基因集和microRNA网络:来自RNA测序的诊断和治疗见解。

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Dao-Jian Xu, Guo-Tao Wang, Qiang Zhong
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引用次数: 0

摘要

肠缺血再灌注损伤(IIRI)是一个复杂而严重的以氧化应激、炎症和细胞凋亡为特征的病理生理过程。近年来,细胞外基质(ECM)基因和microRNAs (miRNAs)在IIRI中的关键作用引起了广泛关注。本文旨在系统总结ECM基因集和miRNA调控网络在IIRI中的诊断和治疗潜力。首先,我们回顾了IIRI的分子机制,重点介绍了ECM在组织损伤和修复过程中的双重作用。深入分析了IIRI进展过程中ECM成分胶原蛋白、弹性蛋白、基质金属蛋白酶等的表达变化及功能。其次,我们系统总结了mirna在IIRI中的调节作用,特别是miR-125b和miR-200a等mirna在调节炎症、细胞凋亡和ECM重塑中的机制和功能。此外,本文还讨论了基于ECM基因和mirna的潜在诊断生物标志物和治疗策略。我们广泛评估了mirna靶向治疗和ECM成分调节在预防和治疗IIRI中的前景,强调了这些新兴疗法的临床转化潜力。总之,ECM基因集和miRNA调控网络在IIRI中的诊断和治疗潜力为进一步研究提供了新的方向,需要更多的临床和基础研究来验证和扩展这些发现,以改善IIRI患者的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular matrix gene set and microRNA network in intestinal ischemia-reperfusion injury: Insights from RNA sequencing for diagnosis and therapy.

Intestinal ischemia-reperfusion injury (IIRI) is a complex and severe pathophysiological process characterized by oxidative stress, inflammation, and apoptosis. In recent years, the critical roles of extracellular matrix (ECM) genes and microRNAs (miRNAs) in IIRI have garnered widespread attention. This review aims to systematically summarize the diagnostic and therapeutic potential of ECM gene sets and miRNA regulatory networks in IIRI. First, we review the molecular mechanisms of IIRI, focusing on the dual role of the ECM in tissue injury and repair processes. The expression changes and functions of ECM components such as collagen, elastin, and matrix metalloproteinases during IIRI progression are deeply analyzed. Second, we systematically summarize the regulatory roles of miRNAs in IIRI, particularly the mechanisms and functions of miRNAs such as miR-125b and miR-200a in regulating inflammation, apoptosis, and ECM remodeling. Additionally, this review discusses potential diagnostic biomarkers and treatment strategies based on ECM genes and miRNAs. We extensively evaluate the prospects of miRNA-targeted therapy and ECM component modulation in preventing and treating IIRI, emphasizing the clinical translational potential of these emerging therapies. In conclusion, the diagnostic and therapeutic potential of ECM gene sets and miRNA regulatory networks in IIRI provides new directions for further research, necessitating additional clinical and basic studies to validate and expand these findings for improving clinical outcomes in IIRI patients.

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