...
首页> 外文期刊>Expert opinion on therapeutic targets >MicroRNA and receptor mediated signaling pathways as potential therapeutic targets in heart failure
【24h】

MicroRNA and receptor mediated signaling pathways as potential therapeutic targets in heart failure

机译:MicroRNA和受体介导的信号通路是心力衰竭的潜在治疗靶点

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: Cardiac remodelling is a complex pathogenetic pathway involving genome expression, molecular, cellular, and interstitial changes that cause changes in size, shape and function of the heart after cardiac injury.Areas covered: We will review recent advances in understanding the role of several receptor-mediated signaling pathways and micro-RNAs, in addition to their potential as candidate target pathways in the pathogenesis of heart failure. The myocyte is the main target cell involved in the remodelling process via ischemia, cell necrosis and apoptosis (by means of various receptor pathways), and other mechanisms mediated by micro-RNAs. We will analyze the role of some receptor mediated signaling pathways such as natriuretic peptides, mediators of glycogen synthase kinase 3 and ERK1/2 pathways, beta-adrenergic receptor subtypes and relaxin receptor signaling mechanisms, TNF/TNF receptor family and TWEAK/Fn14 axis, and some micro-RNAs as candidate target pathways in pathogenesis of heart failure. These mediators of receptor-mediated pathways and micro-RNA are the most addressed targets of emerging therapies in modern heart failure treatment strategies.Expert opinion: Future treatment strategies should address mediators involved in multiple steps within heart failure pathogenetic pathways.
机译:简介:心脏重塑是一个复杂的致病性途径,涉及基因组表达,分子,细胞和间质变化,这些变化会导致心脏损伤后心脏的大小,形状和功能发生变化。受体介导的信号通路和微RNA,以及它们在心力衰竭的发病机理中作为候选靶标通路的潜力。心肌细胞是通过缺血,细胞坏死和凋亡(通过各种受体途径)以及由微小RNA介导的其他机制参与重塑过程的主要靶细胞。我们将分析某些受体介导的信号传导途径的作用,例如利钠肽,糖原合酶激酶3和ERK1 / 2途径的介体,β-肾上腺素能受体亚型和松弛素受体的信号传导机制,TNF / TNF受体家族和TWEAK / Fn14轴,和一些微小RNA作为心力衰竭发病机制的候选靶途径。受体介导途径和微RNA的这些介体是现代心力衰竭治疗策略中新兴疗法中最受关注的目标。专家意见:未来的治疗策略应针对心力衰竭致病途径中涉及多个步骤的介体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号