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Updated: May 31, 2026

Refined Murine Model of Idiopathic Pulmonary Fibrosis
Published on: June 17, 2025
Metalloproteinases in idiopathic pulmonary fibrosis
R C A Dancer1, A M Wood, D R Thickett
1Respiratory Medicine, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK.
Abstract:
In this article, we outline the current state of knowledge about the balance between collagen production and degradation in idiopathic pulmonary fibrosis (IPF). The dysregulated action of metalloproteinases implicated in IPF may play a central role in IPF pathogenesis. Inhibiting metalloproteinases in IPF may, therefore, have therapeutic potential, but our knowledge of their pathophysiological role is held back by limited animal models and the lack of specific inhibitors.
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