ULK1 as a therapeutic target in kidney diseases: Current perspective.

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Expert Opinion on Therapeutic Targets Pub Date : 2024-10-01 Epub Date: 2024-11-11 DOI:10.1080/14728222.2024.2421762
Shruti Shreya, Neha Dagar, Vishwadeep Shelke, Bhupendra Puri, Anil Bhanudas Gaikwad
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Abstract

Introduction: Globally, ~850 million people are affected by different kidney diseases. The pathogenesis of kidney diseases is intricate, where autophagy is crucial for maintaining kidney homeostasis. Iteliminates damaged organelles, thus reducing renal lesions and allowing tissue regeneration. Therefore, targeting various autophagy proteins, e.g. Unc-51-like autophagy-activating kinase 1 (ULK1), is emerging as potential therapeutic strategy against kidney disease.

Areas covered: This review provides insights into the role of ULK1 as a therapeutic target in kidney diseases. Additionally, we have discussed the recent evidence based on pre-clinical studies for possible novel therapies modulating ULK1-mediated autophagy in kidney diseases.

Expert opinion: ULK1 is one of the critical regulators of autophagy. Moreover, ULK1 works differently for different types of kidney disease. Considering its significant role in kidney disease pathogenesis, it could be a potential target to tackle kidney diseases. However, the dynamic molecular understanding of ULK1 in the context of various kidney diseases is still in its infancy and should be investigated further.

作为肾脏疾病治疗靶点的 ULK1:当前视角。
导言:全球约有 8.5 亿人受到不同肾脏疾病的影响。肾脏疾病的发病机制错综复杂,其中自噬是维持肾脏平衡的关键。它能清除受损的细胞器,从而减少肾脏病变,促进组织再生。因此,以各种自噬蛋白(如 Unc-51-like autophagy-activating kinase 1 (ULK1))为靶点正在成为肾脏疾病的潜在治疗策略:本综述深入探讨了 ULK1 作为肾脏疾病治疗靶点的作用。此外,我们还讨论了基于临床前研究的最新证据,即在肾脏疾病中调节 ULK1 介导的自噬的可能新型疗法:ULK1是自噬的关键调节因子之一。此外,ULK1对不同类型的肾脏疾病起着不同的作用。考虑到ULK1在肾脏疾病发病机制中的重要作用,它可能成为应对肾脏疾病的潜在靶点。然而,对 ULK1 在各种肾脏疾病中的动态分子认识仍处于起步阶段,有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
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