Abstract

A potential strategy for diagnosing lung cancer, the leading cause of cancer-related death, is to identify metabolic signatures (biomarkers) of the disease. Although data supports the hypothesis that volatile compounds can be detected in the breath of lung cancer patients by the sense of smell or through bioanalytical techniques, analysis of breath samples is cumbersome and technically challenging, thus limiting its applicability. The hypothesis explored here is that variations in small molecular weight volatile organic compounds (“odorants”) in urine could be used as biomarkers for lung cancer. To demonstrate the presence and chemical structures of volatile biomarkers, we studied mouse olfactory-guided behavior and metabolomics of volatile constituents of urine. Sensor mice could be trained to discriminate between odors of mice with and without experimental tumors demonstrating that volatile odorants are sufficient to identify tumor-bearing mice. Consistent with this result, chemical analyses of urinary volatiles demonstrated that the amounts of several compounds were dramatically different between tumor and control mice. Using principal component analysis and supervised machine-learning, we accurately discriminated between tumor and control groups, a result that was cross validated with novel test groups. Although there were shared differences between experimental and control animals in the two tumor models, we also found chemical differences between these models, demonstrating tumor-based specificity. The success of these studies provides a novel proof-of-principle demonstration of lung tumor diagnosis through urinary volatile odorants. This work should provide an impetus for similar searches for volatile diagnostic biomarkers in the urine of human lung cancer patients.

Highlights

  • Lung cancer is the leading cause of cancer-related deaths throughout most of the world [1]

  • Once we had established this was possible, we employed metabolic profiling to show we could identify specific patterns of volatiles in urine that could distinguish tumor-bearing mice from control animals

  • We used two mouse lung cancer cell lines, LKR that was derived from a transgenic animal expressing mutated Kras and LLC, the Lewis lung cell carcinoma which arose spontaneously

Read more

Summary

Introduction

Lung cancer is the leading cause of cancer-related deaths throughout most of the world [1]. One attractive strategy would be to combine a sensitive imaging technique with a biomarker of lung cancer to increase specificity [6,7,8]. Because the incidence of lung cancer in this ‘‘nodule population’’ is significantly higher than in current or former smoking populations, biomarkers in this context would not require the extremely high sensitivities and specificities needed for population screening. Another use for such a biomarker might be to follow the course of the tumor after treatment

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call