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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2026, Vol. 31 ›› Issue (5): 709-715.doi: 10.12092/j.issn.1009-2501.2026.05.016

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Research progress of Hippo pathway effector YAP/TAZ in idiopathic pulmonary fibrosis

Haodong YANG1(), Long LI2,*(), Jingxuan LUO1, Jinglei LI1   

  1. 1. The First Clinical Medical College of Lanzhou University, Lanzhou 730000, Gansu, China
    2. Department of Respiratory Medicine, the First Hospital of Lanzhou University, Lanzhou 730000, Gansu, China
  • Received:2025-01-22 Revised:2025-04-10 Online:2026-05-26 Published:2026-06-02
  • Contact: Long LI E-mail:yhd0713@163.com;llqqdbd@163.com

Abstract:

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, age-related, irreversible and fibrotic interstitial lung disease. The median survival time after the diagnosis of IPF is only 2-5 years. It is characterized by the process of fibroblast proliferation, extracellular matrix deposition and dysregulated alveolar epithelial repair. Currently, there is no definite and significantly effective treatment. More and more evidence indicates that the Hippo signaling pathway is closely related to idiopathic pulmonary fibrosis (IPF). This article reviews the current research status of Hippo signaling pathway effector factors YAP/TAZ in pulmonary fibrosis and the research results of existing inhibitors to intervene YAP/TAZ to delay pulmonary fibrosis, in order to provide a reference for the treatment of pulmonary fibrosis.

Key words: idiopathic pulmonary fibrosis, Hippo signaling pathway, YAP/TAZ, fibroblasts, alveolar epithelial cells

CLC Number: