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Update of Aging Hallmarks in Idiopathic Pulmonary Fibrosis

5 Feb 2025

Abstract excerpt

Idiopathic Pulmonary Fibrosis (IPF) is an epithelial-driven interstitial lung disease of unknown etiology characterized by the excessive proliferation of fibroblast populations that synthesize large amounts of extracellular matrix. In this devastating disorder, all aging hallmarks appear prematurely or are altered. This review highlights key findings about IPF characteristics recently recognized as hallmarks of...

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Share to Chronic Obstructive Pulmonary Disease (COPD) Research
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PMID: 39937013
DOI: 10.3390/cells14030222

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