Beyond TGFβ - Novel ways to target airway and parenchymal fibrosis

被引:15
作者
Boorsma, C. E. [1 ,2 ]
Dekkers, B. G. J. [2 ,3 ]
van Dijk, E. M. [2 ,4 ]
Kumawat, K. [2 ,4 ]
Richardson, J. [5 ]
Burgess, J. K. [6 ,7 ]
John, A. E. [8 ]
机构
[1] Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
[4] Univ Groningen, Dept Mol Pharmacol, Groningen, Netherlands
[5] Univ Nottingham Hosp, Div Resp Med, Nottingham NG7 2UH, England
[6] Woolcock Inst Med Res, Glebe, NSW 2037, Australia
[7] Univ Sydney, Discipline Pharmacol, Sydney, NSW 2006, Australia
[8] Univ Nottingham Hosp, Div Resp Med, Nottingham NG5 1PB, England
基金
英国医学研究理事会;
关键词
Fibrosis; Airway; Parenchyma; IPF; COPD; Asthma; IDIOPATHIC PULMONARY-FIBROSIS; TISSUE GROWTH-FACTOR; HUMAN LUNG FIBROBLASTS; WNT1-INDUCIBLE SIGNALING PROTEIN-1; EXTRACELLULAR-MATRIX PRODUCTION; PROTEASE-ACTIVATED RECEPTOR-1; SMOOTH-MUSCLE PHENOTYPE; ANGIOTENSIN-II; SPHINGOSINE; 1-PHOSPHATE; ALVEOLAR MACROPHAGES;
D O I
10.1016/j.pupt.2014.08.009
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Within the lungs, fibrosis can affect both the parenchyma and the airways. Fibrosis is a hallmark pathological change in the parenchyma in patients with idiopathic pulmonary fibrosis (IPF), whilst in asthma or chronic obstructive pulmonary disease (COPD) fibrosis is a component of the remodelling of the airways. In the past decade, significant advances have been made in understanding the disease behaviour and pathogenesis of parenchymal and airway fibrosis and as a result a variety of novel therapeutic targets for slowing or preventing progression of these fibrotic changes have been identified. This review highlights a number of these targets and discusses the potential for treating parenchymal or airway fibrosis through these mediators/pathways in the future. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 180
页数:15
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