Wnt/β-连环蛋白信号传导与肾脏和泌尿道先天性异常。

IF 3.2 4区 医学 Q1 UROLOGY & NEPHROLOGY
Kidney Diseases Pub Date : 2024-10-03 eCollection Date: 2024-12-01 DOI:10.1159/000541684
Cuicui Yu, Bixia Zheng, Luyan Zhang, Aihua Zhang, Zhanjun Jia, Guixia Ding
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引用次数: 0

摘要

背景:在胚胎发生过程中,细胞间通讯的精确调控对细胞存活和正常功能至关重要。Wnt蛋白家族是一个高度保守且被广泛研究的群体,在细胞发育和再生的关键细胞信号事件中起着至关重要的作用。先天性肾脏和尿路异常(ckut)是儿童和年轻人慢性肾脏疾病的主要原因,包括胚胎发育期间由生殖泌尿道发育中断引起的各种出生异常。CAKUT的发生和发展可能与Wnt信号转导机制有关。摘要:本文综述了经典Wnt信号通路在CAKUT中的作用,探讨了相关的分子机制,为今后的治疗提供了新的靶点和干预方法。关键信息:Wnt信号复杂地参与肾脏发育过程中的多种分化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wnt/β-Catenin Signaling and Congenital Abnormalities of Kidney and Urinary Tract.

Background: Precise regulation of cell-cell communication is vital for cell survival and normal function during embryogenesis. The Wnt protein family, a highly conserved and extensively studied group, plays a crucial role in key cell-cell signaling events essential for development and regeneration. Congenital anomalies of the kidney and urinary tract (CAKUT) represent a leading cause of chronic kidney disease in children and young adults, and include a variety of birth abnormalities resulting from disrupted genitourinary tract development during embryonic development. The incidence and progression of CAKUT may be related to the Wnt signal transduction mechanism.

Summary: This review provides a comprehensive overview of the classical Wnt signaling pathway's role in CAKUT, explores related molecular mechanisms and provides new targets and intervention methods for the future treatment of the disease.

Key messages: The Wnt signal is intricately engaged in a variety of differentiation processes throughout kidney development.

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来源期刊
Kidney Diseases
Kidney Diseases UROLOGY & NEPHROLOGY-
CiteScore
6.00
自引率
2.70%
发文量
33
审稿时长
27 weeks
期刊介绍: ''Kidney Diseases'' aims to provide a platform for Asian and Western research to further and support communication and exchange of knowledge. Review articles cover the most recent clinical and basic science relevant to the entire field of nephrological disorders, including glomerular diseases, acute and chronic kidney injury, tubulo-interstitial disease, hypertension and metabolism-related disorders, end-stage renal disease, and genetic kidney disease. Special articles are prepared by two authors, one from East and one from West, which compare genetics, epidemiology, diagnosis methods, and treatment options of a disease.
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