MERTK and Fibrosis: A New Target for Therapy.

DNA and cell biology Pub Date : 2024-07-01 Epub Date: 2024-05-31 DOI:10.1089/dna.2024.0099
Ziyan Pan, Mohammed Eslam
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Abstract

Organ fibrosis is a devastating medical challenge that is collectively responsible for an estimated 45% of all deaths in developed countries and poses a substantial health and economic burden. The process of fibrosis has common characteristics that can occur in various organs, such as the liver, kidney, lung, and skin. Currently, there is a paucity of effective treatments available for fibrosis. Therefore, it is crucial to identify new approaches to find potential therapeutic targets. Genetic studies have shown great promise in advancing the drug development process. Mer tyrosine kinase (MERTK) was recently identified as a crucial regulator of fibrosis that specifically controls the activity of transforming growth factor beta (TGFβ). In this brief review, we provide an overview of the potential role of MERTK as a targeted and valuable approach for treating organ fibrosis.

MERTK与纤维化:治疗的新靶点
器官纤维化是一项毁灭性的医学挑战,在发达国家,估计有 45% 的死亡是由器官纤维化共同造成的,并带来了巨大的健康和经济负担。肝、肾、肺和皮肤等不同器官的纤维化过程具有共同特征。目前,治疗肝纤维化的有效方法很少。因此,找出潜在的治疗靶点的新方法至关重要。基因研究在推进药物开发过程中显示出巨大的前景。最近,Mer酪氨酸激酶(MERTK)被确认为纤维化的一个重要调节因子,它专门控制转化生长因子β(TGFβ)的活性。在这篇简短的综述中,我们将概述 MERTK 作为治疗器官纤维化的一种有价值的靶向方法的潜在作用。
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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