Involvement of E3 ubiquitin ligase NEDD4-mediated YY1 ubiquitination in alleviating idiopathic pulmonary fibrosis

L Chen, Q Sun, R Yue, H Yan, X Huang, H Yu… - International Journal of …, 2024 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a chronic and lethal lung disease characterized by
progressive lung scarring. This study aims to elucidate the role of the E3 ubiquitin ligase …

[HTML][HTML] NEDD4L-induced β-catenin ubiquitination suppresses the formation and progression of interstitial pulmonary fibrosis via inhibiting the CTHRC1/HIF-1α axis

L Chen, Y Yang, H Yan, X Peng… - International Journal of …, 2021 - ncbi.nlm.nih.gov
Interstitial pulmonary fibrosis (IPF) is a severe progressive lung disease with limited
therapeutic options and poor prognosis. Initially, we found the downregulated level of neural …

Conditional deletion of Nedd4-2 in lung epithelial cells causes progressive pulmonary fibrosis in adult mice

J Duerr, DHW Leitz, M Szczygiel, D Dvornikov… - Nature …, 2020 - nature.com
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease
characterized by patchy scarring of the distal lung with limited therapeutic options and poor …

Nedd4L suppression in lung fibroblasts facilitates pathogenesis of lung fibrosis

S Li, Q Ye, J Wei, SJ Taleb, H Wang, Y Zhang… - Translational …, 2023 - Elsevier
Ubiquitination-mediated protein degradation is associated with the development of
pulmonary fibrosis. We and others have shown that Nedd4L plays anti-inflammatory and anti …

Yin yang 1 is a novel regulator of pulmonary fibrosis

X Lin, PJ Sime, H Xu, MA Williams… - American journal of …, 2011 - atsjournals.org
Rationale: The differentiation of fibroblasts into myofibroblasts is a cardinal feature of
idiopathic pulmonary fibrosis (IPF). The transcription factor Yin Yang 1 (YY1) plays a role in …

YY1 mediates TGF-β1-induced EMT and pro-fibrogenesis in alveolar epithelial cells

C Zhang, X Zhu, Y Hua, Q Zhao, K Wang, L Zhen… - Respiratory …, 2019 - Springer
Pulmonary fibrosis is a chronic, progressive lung disease associated with lung damage and
scarring. The pathological mechanism causing pulmonary fibrosis remains unknown …

[HTML][HTML] Ubiquitination and deubiquitination emerge as players in idiopathic pulmonary fibrosis pathogenesis and treatment

S Li, J Zhao, D Shang, DJ Kass, Y Zhao - JCI insight, 2018 - ncbi.nlm.nih.gov
Idiopathic pulmonary fibrosis (IPF) is a fatal fibrotic lung disease that is associated with
aberrant activation of TGF-β, myofibroblast differentiation, and abnormal extracellular matrix …

Development of pulmonary fibrosis in conditional Nedd4-2 deficient mice

D Leitz, J Duerr, D Dvornikov, M Szczygiel, P Konietzke… - 2018 - Eur Respiratory Soc
Idiopahtic pulmonary firbosis (IPF) is a severe lung disease of unknown etiology with a poor
prognosis and limited therapeutic options. In this study, we characterized a mouse model …

Reduced ets domain-containing protein Elk1 promotes pulmonary fibrosis via increased integrin αvβ6 expression

AL Tatler, A Habgood, J Porte, AE John… - Journal of Biological …, 2016 - ASBMB
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with high mortality.
Active TGFβ1 is considered central to the pathogenesis of IPF. A major mechanism of TGFβ1 …

Inactivation of nuclear histone deacetylases by EP300 disrupts the MiCEE complex in idiopathic pulmonary fibrosis

K Rubio, I Singh, S Dobersch, P Sarvari… - Nature …, 2019 - nature.com
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and highly lethal lung disease
with unknown etiology and poor prognosis. IPF patients die within 2 years after diagnosis …