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Exhaled breath condensate identifies metabolic dysregulation in patients with radiation-induced lung injury.

Authors :
Odoom, Josly Pierre-Louis
Freeberg, Margaret A. T.
Camus, Sarah V.
Toft, Robin
Szomju, Barbara B.
Sanchez Rosado, Rose Marie
Jackson, Peter D.
Allegood, Jeremy C.
Silvey, Scott
Jinze Liu
Cowart, L. Ashley
Weiss, Elisabeth
Thatcher, Thomas H.
Sime, Patricia J.
Source :
American Journal of Physiology: Lung Cellular & Molecular Physiology. Jun2023, Vol. 324 Issue 6, pL863-L869. 7p.
Publication Year :
2023

Abstract

Radiation-induced lung injury (RILI) is a consequence of therapeutic thoracic irradiation (TR) for many cancers, and there are no FDA-approved curative strategies. Studies report that 80% of patients who undergo TR will have CT-detectable interstitial lung abnormalities, and strategies to limit the risk of RILI may make radiotherapy less effective at treating cancer. Our lab and others have reported that lung tissue from patients with idiopathic pulmonary fibrosis (IPF) exhibits metabolic defects including increased glycolysis and lactate production. In this pilot study, we hypothesized that patients with radiation-induced lung damage will exhibit distinct changes in lung metabolism that may be associated with the incidence of fibrosis. Using liquid chromatography/tandem mass spectrometry to identify metabolic compounds, we analyzed exhaled breath condensate (EBC) in subjects with CT-confirmed lung lesions after TR for lung cancer, compared with healthy subjects, smokers, and cancer patients who had not yet received TR. The lung metabolomic profile of the irradiated group was significantly different from the three nonirradiated control groups, highlighted by increased levels of lactate. Pathway enrichment analysis revealed that EBC from the case patients exhibited concurrent alterations in lipid, amino acid, and carbohydrate energy metabolism associated with the energy-producing tricarboxylic acid (TCA) cycle. Radiation-induced glycolysis and diversion of lactate to the extracellular space suggests that pyruvate, a precursor metabolite, converts to lactate rather than acetyl-CoA, which contributes to the TCA cycle. This TCA cycle deficiency may be compensated by these alternate energy sources to meet the metabolic demands of chronic wound repair. Using an "omics" approach to probe lung disease in a noninvasive manner could inform future mechanistic investigations and the development of novel therapeutic targets. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10400605
Volume :
324
Issue :
6
Database :
Academic Search Index
Journal :
American Journal of Physiology: Lung Cellular & Molecular Physiology
Publication Type :
Academic Journal
Accession number :
164295217
Full Text :
https://doi.org/10.1152/ajplung.00439.2022