Breath biopsy for early detection and precision medicine in cancer
Marc van der Schee, Hazel Pinheiro and Edoardo Gaude
Owlstone Medical Ltd, 183 Science Park, Cambridge, CB4 0GJ, UK
Corresponding author: Marc van der Schee. E-mail: Marc.vanderSchee@owlstone.co.uk
Abstract
Breath biopsy enables the non-invasive collection and analysis of volatile organic compounds (VOCs) in exhaled breath, providing valuable information about disease processes occurring in the body. Metabolic changes occur in cancer cells at the earliest stages of disease. We discuss progress in the use of breath biopsy for discovery of breath-based biomarkers for early detection of cancer, and potential applications for breath biopsy in enabling precision medicine in cancer.
Keywords: biomarkers, breath, breathomics, precision medicine, personalised medicine, metabolism, lung cancer, colorectal cancer, oncogenesis, Warburg effect, early detection, metabolomics
Copyright: © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Published: 19/07/2018; Received: 01/03/2018
Introduction
Every breath contains a wealth of valuable information about the health of an individual, in the form of volatile organic compounds, or VOCs. Whereas genomic analysis provides information about disease predisposition, in reality disease is the result of multiple interacting genetic and environmental factors. The body’s metabolome is affected by all of these factors, and as such provides real time information which is closely related to actual disease activity.
Capturing VOCs in breath via a simple ‘breath biopsy’ provides a completely non-invasive means to analyse volatile metabolites produced by metabolic processes occurring throughout the body. Over 1,000 VOCs in breath have already been identified [1], representing a source of promising biomarkers for a wide range of diseases, including cancer.
With applications in early detection and precision medicine, breath biopsy has the potential to address two fundamental challenges in oncology today: firstly, early diagnosis of cancer patients, and secondly, precision medicine – ensuring patients receive the treatment which is most effective for them.
Breath biomarkers for early detection of cancer
Cancer cells undergo profound changes in their metabolism in order to support high energetic demands of uncontrolled proliferation [2]. Several oncogenic mutations have been shown to affect the metabolism of cancer cells by converging to common metabolic pathways linked to cell cycle and anabolic growth [3–5]. The Warburg effect is among the well-established cancer metabolic hallmarks [6] and entails the activation of aerobic glycolysis as the main pathway for biosynthetic purposes, as opposed to normal cells that exploit mitochondrial metabolism for their energetic needs [7, 8].
These changes in cellular metabolism favour survival in an oxygen deprived environment and result in altered metabolic intermediates that function as the building blocks for new cells, both enabling the growth of rapidly dividing cancer cells, and also altering the profile of VOCs in breath [9]. As these processes are fundamental to cancer cell survival, such altered cellular metabolism occurs as one of the earliest stages of tumourigenesis [10–12], hence VOCs are excellent candidate biomarkers for early detection of cancer.
Reproducible breath collection in a clinical setting has been historically challenging, for example due to the use of polymer storage bags which result in low sensitivity for VOC detection, loss of VOCs through the bag, contamination with external VOCs, variable collection volumes, and carry-over on re-used materials [13], however a breath collection device developed in collaboration with over 100 breath diagnostics researchers [14] is now enabling the world’s largest breath-based clinical trial evaluating breath biopsy for early detection of lung cancer. The UK NHS funded LuCID trial (ClinicalTrials.gov identifier NCT02612532) [15] will recruit up to 4,000 patients, referred with clinical suspicion of lung cancer, and aims to identify a VOC biomarker signature in breath that can distinguish the presence or absence of lung cancer. It is hoped that a breath test would augment existing lung cancer screening techniques. Low-dose computed tomography (LDCT) suffers from a high rate of false positive results [16]. A breath biopsy test as a rule-in test would reduce unnecessary CT scans and invasive follow up procedures, reducing screening costs and increasing health benefits.
Breath biopsy is also being deployed in large scale clinical studies to identify biomarkers for the early detection of colorectal cancer (InTERCEPT project [17], involving up to 1,000 patients in collaboration with Warwick University and the University Hospital Coventry and Warwickshire NHS Trust) and multiple cancer types (PAN Cancer Study [18], in collaboration with Cancer Research UK).
Precision medicine applications for breath biopsy
Since the VOC profile closely reflects metabolic processes, VOC biomarkers are well positioned to provide insight into the biological variability underlying disease processes. The potential for breath biomarkers in precision medicine applications has been mostly explored in the area of respiratory diseases such as asthma and COPD [19], and evidence suggesting VOCs in breath can differentiate between different subtypes of cancer [20] points towards the utility of breath biomarkers for precision medicine in cancer.
Metabolic pathways themselves are targets for the development of novel cancer therapies [21, 22], raising the possibility that breath biomarkers reflecting the target metabolic pathway may in future be used to stratify patients, enabling therapies to be directed to the patients most likely to benefit. Monitoring changes in the breath VOC profile before and during treatment could provide confirmation of therapy efficacy by tracking changes in disease-related VOC biomarkers, enabling treatment to be avoided or discontinued quickly if a lack of response is identified. Measuring specific drug-related volatile metabolites in breath may also provide valuable information about how a drug is being metabolised by the patient, which could be related to therapeutic response.
Continued mutations in cancer cells result in considerable heterogeneity in the tumour. Therapy failure is often associated with clonal expansion of a specific subset of tumour cells. The associated metabolic reprogramming [21, 23, 24], suggests that metabolic biomarkers could provide predictive information about therapy failure. Indeed, several lines of evidence indicate that metabolic flexibility is an important determinant of resistance to cancer therapies [25]. There is evidence from metabolomics analysis of tissue in pancreatic ductal adenocarcinoma patients that metabolic biomarkers may be predictive of resistance to the chemotherapy gemcitabine [26]. Metabolic changes may also be associated with drug-induced toxicity [27, 28], suggesting that VOC biomarkers in breath could be explored as potential predictors of toxicity.
Research is beginning to uncover the impact of the microbiome on oncogenesis and the efficacy of cancer therapies [29]. Recently, intratumour bacteria have been reported to metabolise a chemotherapeutic drug, leading to resistance [30]. The microbiome contributes to the body’s metabolome, and hence the profile of VOCs in breath can be analysed as a non-invasive means to discover biomarkers that reflect the activity or involvement of the microbiome in cancer.
Conclusions
Breath biopsy provides a non-invasive way to capture and analyse volatile metabolites in breath, and gain a rapid insight into the metabolic changes associated with cancer from the earliest stages of disease. Large scale clinical trials are underway to evaluate breath biopsy for the early detection of multiple different tumour types. Building on the technological advances in breath collection and analysis that have been established, we can now begin to explore how breath biomarkers could help guide treatment decisions in a personalised medicine approach, for example by predicting drug resistance, toxicity and therapeutic response. Breath biopsy tests have the potential to revolutionise healthcare, enabling patients to be monitored over time without incurring significant costs or radiation exposure. The non-invasive nature of a breath test will ensure acceptability for patients, increasing uptake for screening programmes.
References
1. de Lacy Costello B, Amann A, and Al-Kateb H, et al (2014) A review of the volatiles from the healthy human body J Breath Res 8 14001
2. Pavlova NN and Thompson CB (2016) The emerging hallmarks of cancer metabolism Cell Metab 23 27–47
3. Nagarajan A, Malvi P, and Wajapeyee N (2016) Oncogene-directed alterations in cancer cell metabolism Trends Cancer 2 365–377
4. Hu J, Locasale JW, and Bielas JH, et al (2013) Heterogeneity of tumor-induced gene expression changes in the human metabolic network Nat Biotechnol 31 522–529
5. Gaude E and Frezza C (2016) Tissue-specific and convergent metabolic transformation of cancer correlates with metastatic potential and patient survival. Nat Commun 7 13041
6. Warburg O (1956) On the origin of cancer cells Science 123 309–314
7. Cantor JR and Sabatini DM (2012) Cancer cell metabolism: one hallmark, many faces Cancer Discov 2 881–898
8. Vander Heiden MG, Cantley LC, and Thompson CB (2009) Understanding the Warburg effect: the metabolic requirements of cell proliferation Science 324 1029–1033
9. Feinberg T, Alkoby-Meshulam L, and Herbig J, et al (2016) Cancerous glucose metabolism in lung cancer—evidence from exhaled breath analysis J Breath Res 10 26012
10. Ying H, Kimmelman AC, and Lyssiotis CA, et al (2012) Oncogenic Kras maintains pancreatic tumors through regulation of anabolic glucose metabolism Cell 149 656–670
11. Shain AH, Yeh I, and Kovalyshyn I, et al (2015) The genetic evolution of melanoma from precursor lesions N Engl J Med 373 1926–1936
12. Satoh K, Yachida S, and Sugimoto M, et al (2017) Global metabolic reprogramming of colorectal cancer occurs at adenoma stage and is induced by MYC Proc Natl Acad Sci U S A 114 E7697–E7706
13. Beauchamp J, Herbig J, and Gutmann R, et al (2008) On the use of Tedlar® bags for breath-gas sampling and analysis J Breath Res 2(4) 046001 [doi:10.1088/1752-7155/2/4/046001]
14. Breathe Free Consortium [www.breathe-free.org] Date accessed: 28/02/18
15. Van der Schee M, Dickson J, and Ruparel M, et al (2017) P3.05-001 breath analysis for early detection of lung cancer: the LuCID study J Thorac Oncol 12 S2290
16. National Lung Screening Trial Research Team, Aberle DR, and Adams AM, et al (2011) Reduced lung-cancer mortality with low-dose computed tomographic screening N Engl J Med 365 395–409
17. InTERCEPT [https://www.owlstonemedical.com/clinical-pipeline/intercept/] Date accessed: 28/02/18
18. PAN Cancer Study [https://www.owlstonemedical.com/about/news/2017/jul/10/pan-cancer-trial/] Date accessed: 28/02/18
19. Bos LD, Sterk PJ, and Fowler SJ (2016) Breathomics in the setting of asthma and chronic obstructive pulmonary disease J Allergy Clin Immunol 138 970–976
20. Barash O, Zhang W, and Halpern JM, et al (2015) Differentiation between genetic mutations of breast cancer by breath volatolomics Oncotarget 6 44864–44876
21. Tennant DA, Durán RV, and Gottlieb E (2010) Targeting metabolic transformation for cancer therapy Nat Rev Cancer 10 267–277
22. Martinez-Outschoorn UE, Peiris-Pagés M, and Pestell RG, et al (2017) Cancer metabolism: a therapeutic perspective Nat Rev Clin Oncol 14 11–31
23. Pan Y, Cao M, and Liu J, et al (2017) Metabolic regulation in mitochondria and drug resistance Adv Exp Med Biol 1038 149–171
24. Biswal BN, Das SN, and Das BK, et al (2017) Alteration of cellular metabolism in cancer cells and its therapeutic prospects J Oral Maxillofac Pathol 21 244–251
25. Valcarcel-Jimenez L, Gaude E, and Torrano V, et al (2017) Mitochondrial metabolism: Yin and Yang for tumor progression Trends Endocrinol Metab 28 748–757
26. Phua LC, Goh S, and Tai DWM, et al (2018) Metabolomic prediction of treatment outcome in pancreatic ductal adenocarcinoma patients receiving gemcitabine Cancer Chemother Pharmacol 81 277–289
27. Loizou GD (2016) Animal-free chemical safety assessment Front Pharmacol 7 218
28. Chaudhari U, Ellis JK, and Wagh V, et al (2017) Metabolite signatures of doxorubicin induced toxicity in human induced pluripotent stem cell-derived cardiomyocytes Amino Acids 49 1955–1963
29. Johnson CH, Spilker ME, and Goetz L, et al (2016) Metabolite and microbiome interplay in cancer immunotherapy Cancer Res 76 6146–6152
30. Geller LT, Barzily-Rokni M, and Danino T, et al (2017) Potential role of intratumor bacteria in mediating tumor resistance to the chemotherapeutic drug gemcitabine Science 357 1156–1160