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Urinary Volatilomic Signatures for Non-Invasive Detection of Lung Cancer: A HS-SPME/GC-MS Proof-of-Concept Study
Patrícia Sousa1, Pedro H Berenguer1,2, Catarina Luís1,3
1CQM-Centro de Química da Madeira, Universidade da Madeira, Campus da Penteada, 9020-105 Funchal, Portugal.
This study identifies a unique urinary volatile organic compound signature for lung cancer (LC) detection. These findings suggest a non-invasive method for early lung cancer diagnosis using gas chromatography-mass spectrometry.
Area of Science:
- Biochemistry
- Analytical Chemistry
- Oncology
Background:
- Lung cancer (LC) is a leading cause of cancer death, often diagnosed late.
- Current screening methods for LC have limited performance.
- Urinary volatile organic compounds (VOCs) offer a potential non-invasive biomarker source.
Purpose of the Study:
- To characterize the urinary volatilome in lung cancer patients and healthy controls.
- To identify a distinct LC-associated volatilomic signature.
- To discover volatile organic metabolites (VOMs) with potential as diagnostic biomarkers for LC.
Main Methods:
- Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME/GC-MS) was employed.
- The urinary volatilome of 56 lung cancer patients and healthy controls was analyzed.
- Multivariate statistical analyses, including partial least squares-discriminant analysis (PLS-DA), were used for classification.
Main Results:
- A distinct metabolic profile was observed between lung cancer patients and healthy controls.
- LC patients showed elevated levels of terpenoids and aldehydes, indicative of oxidative stress.
- Healthy controls exhibited a predominance of sulfur-containing compounds and volatile phenols.
- Octanal, dehydro-p-cymene, 2,6-dimethyl-7-octen-2-ol, and 3,7-dimethyl-3-octanol were identified as potent discriminatory VOMs.
Conclusions:
- Urinary volatilomic profiling using HS-SPME/GC-MS can reveal disease-specific molecular signatures.
- This approach shows promise as a non-invasive tool for early lung cancer detection.
- Further validation in independent cohorts and integration into multi-omics frameworks are warranted.
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