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Beyond TGFβ - Novel ways to target airway and parenchymal fibrosis
被引:15
作者:

Boorsma, C. E.
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Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands
Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands

Dekkers, B. G. J.
论文数: 0 引用数: 0
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机构:
Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands
Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands

van Dijk, E. M.
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Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands
Univ Groningen, Dept Mol Pharmacol, Groningen, Netherlands Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands

Kumawat, K.
论文数: 0 引用数: 0
h-index: 0
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Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands
Univ Groningen, Dept Mol Pharmacol, Groningen, Netherlands Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands

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Burgess, J. K.
论文数: 0 引用数: 0
h-index: 0
机构:
Woolcock Inst Med Res, Glebe, NSW 2037, Australia
Univ Sydney, Discipline Pharmacol, Sydney, NSW 2006, Australia Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, Groningen, Netherlands

论文数: 引用数:
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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
相关论文
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