MicroRNA-630: A potential guardian against inflammation in diabetic kidney disease.

IF 4.2 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM World Journal of Diabetes Pub Date : 2024-09-15 DOI:10.4239/wjd.v15.i9.1837
Ashraf Al Madhoun
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Abstract

In this editorial, we comment on the article by Wu et al published "MicroRNA-630 alleviates inflammatory reactions in rats with diabetic kidney disease by targeting toll-like receptor 4". Diabetic kidney disease (DKD) stands as a significant complication occurring from diabetes mellitus, which contributes substantially to the morbidity and mortality rates worldwide. Renal tubular epithelial cell da-mage, often accompanied by inflammatory responses and mesenchymal trans-differentiation, plays a pivotal role in the progression of DKD. Despite extensive research, the intricate molecular mechanisms underlying these processes remain to be determined. Wu et al remarkable work identifies microRNA-630 (miR-630) as an emerging potential regulator of cell migration, apoptosis, and autophagy, prompting investigation into its association with DKD pathogenesis. This study endeavors to elucidate the impact of miR-630 on TEC injury and the inflammatory response in DKD rats. The role of miR-630 in human DKD will be of interest for future studies.

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MicroRNA-630:糖尿病肾病炎症的潜在守护者
在这篇社论中,我们对 Wu 等人发表的文章 "MicroRNA-630 通过靶向收费样受体 4 减轻糖尿病肾病大鼠的炎症反应 "进行了评论。糖尿病肾病(DKD)是糖尿病的重要并发症之一,在全球范围内造成了严重的发病率和死亡率。肾小管上皮细胞变异往往伴随着炎症反应和间质转分化,在糖尿病肾病的发展过程中起着至关重要的作用。尽管进行了大量研究,但这些过程背后错综复杂的分子机制仍有待确定。Wu 等人的杰出研究发现,microRNA-630(miR-630)是细胞迁移、凋亡和自噬的一个新兴潜在调控因子,这促使人们研究它与 DKD 发病机制的关联。本研究试图阐明 miR-630 对 DKD 大鼠 TEC 损伤和炎症反应的影响。未来的研究还将关注 miR-630 在人类 DKD 中的作用。
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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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