肌成纤维细胞
纤维化
医学
转化生长因子
肾脏疾病
肾
细胞外基质
信号转导
癌症研究
生物信息学
内科学
生物
细胞生物学
作者
Cheol Ho Park,Tae‐Hyun Yoo
出处
期刊:Pharmaceuticals
[Multidisciplinary Digital Publishing Institute]
日期:2022-11-29
卷期号:15 (12): 1485-1485
被引量:31
摘要
Kidney fibrosis is a common pathophysiological mechanism of chronic kidney disease (CKD) progression caused by several underlying kidney diseases. Among various contributors to kidney fibrosis, transforming growth factor-β1 (TGF-β1) is the major factor driving fibrosis. TGF-β1 exerts its profibrotic attributes via the activation of canonical and non-canonical signaling pathways, which induce proliferation and activation of myofibroblasts and subsequent accumulation of extracellular matrix. Over the past few decades, studies have determined the TGF-β1 signaling pathway inhibitors and evaluated whether they could ameliorate the progression of CKD by hindering kidney fibrosis. However, therapeutic strategies that block TGF-β1 signaling have usually demonstrated unsatisfactory results. Herein, we discuss the therapeutic concepts of the TGF-β1 signaling pathway and its inhibitors and review the current state of the art regarding regarding TGF-β1 inhibitors in CKD management.
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