Integrative metabolomic and lipidomic profiling of lung squamous cell carcinoma for characterization of metabolites and intact lipid species related to the metastatic potential
- Authors
- Lee, H.; Lee, H.; Park, S.; Kim, M.; Park, J.Y.; Jin, H.; Oh, K.; Bae, J.; Yang, Y.; Choi, H.-K.
- Issue Date
- Aug-2021
- Publisher
- MDPI AG
- Keywords
- DI-MS; GC-MS; Lipidomics; Lung squamous cell carcinoma; Metabolomics; Metastatic potential
- Citation
- Cancers, v.13, no.16
- Journal Title
- Cancers
- Volume
- 13
- Number
- 16
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/49482
- DOI
- 10.3390/cancers13164179
- ISSN
- 2072-6694
2072-6694
- Abstract
- SQCC is a major type of NSCLC, which is a major cause of cancer-related deaths, and there were no reports regarding the prediction of metastatic potential of lung SQCC by metabolomic and lipidomic profiling. In this study, metabolomic and lipidomic profiling of lung SQCC were performed to predict its metastatic potential and to suggest potential therapeutic targets for the inhibition of lung SQCC metastasis. Human bronchial epithelial cells and four lung SQCC cell lines with different metastatic potentials were analyzed using gas chromatography–mass spectrometry and direct infusion-mass spectrometry. Based on the obtained metabolic and lipidomic profiles, we constructed models to predict the metastatic potential of lung SQCC; glycerol, putrescine, β-alanine, hypoxanthine, inosine, myo-inositol, phosphatidylinositol (PI) 18:1/18:1, and PI 18:1/20:4 were suggested as characteristic metabolites and intact lipid species associated with lung SQCC metastatic potential. In this study, we established predictive models for the metastatic potential of lung SQCC; furthermore, we identified metabolites and intact lipid species relevant to lung SQCC metastatic potential that may serve as potential therapeutic targets for the inhibition of lung SQCC metastasis. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
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Collections - College of Pharmacy > School of Pharmacy > 1. Journal Articles

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