Article
Role of lung ornithine aminotransferase in Idiopathic Pulmonary Fibrosis: regulation of mitochondrial ROS generation and TGF-β1 activity
2023-09-27
Abstract excerpt
<title>Abstract</title><p>Idiopathic pulmonary fibrosis (IPF) exhibits aberrant lung remodeling that is characterized by excessive accumulation of extracellular matrix (ECM) proteins. In a previous study, we found that levels of ornithine aminotransferase (OAT), a principal enzyme of the proline metabolic pathway, were elevated in the lungs of patients with IPF. However, the precise role played by OAT in IPF patho...
Topics
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- Advanced Glycation End Products research
- Autophagy in Disease and Therapy
- Cancer-related molecular mechanisms research
- Histone Deacetylase Inhibitors Research
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Medical Imaging and Pathology Studies
- Mesenchymal stem cell research
- Peptidase Inhibition and Analysis
Identifiers and source
- Literature Corpus work
- d2e5a3de-1182-59e4-b393-9fc852b179b8
- DOI
- 10.21203/rs.3.rs-3304833/v1
