Metabolic Signatures of Lung Cancer in Sputum and Exhaled Breath Condensate Detected by H-1 Magnetic Resonance Spectroscopy: A Feasibility Study

被引:23
作者
Ahmed, Naseer [1 ,2 ]
Bezabeh, Tedros [3 ,4 ]
Ijare, Omkar B. [3 ]
Myers, Renelle [5 ]
Alomran, Reem [1 ,2 ]
Aliani, Michel [6 ,7 ]
Nugent, Zoann [1 ]
Banerji, Shantanu [1 ,2 ]
Kim, Julian [1 ,2 ]
Qing, Gefei [8 ]
Bshouty, Zoheir [5 ]
机构
[1] CancerCare Manitoba, Winnipeg, MB, Canada
[2] Univ Manitoba, Winnipeg, MB, Canada
[3] Univ Winnipeg, Dept Chem, Winnipeg, MB, Canada
[4] Univ Guam, Coll Nat & Appl Sci, Mangilao, GU USA
[5] Univ Manitoba, Dept Respirol, Hlth Sci Ctr, Winnipeg, MB, Canada
[6] Univ Manitoba, Dept Human Nutr Sci, Winnipeg, MB, Canada
[7] St Boniface Gen Hosp, Albrechtsen Res Ctr, Winnipeg, MB, Canada
[8] Univ Manitoba, Dept Pathol, Hlth Sci Ctr, Winnipeg, MB, Canada
关键词
magnetic resonance spectroscopy; sputum; breath condensate; lung cancer;
D O I
10.4137/MRI.S40864
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
OBJECTIVES: Lung cancer is one of the most lethal cancers. Currently, there are no biomarkers for early detection, monitoring treatment response, and detecting recurrent lung cancer. We undertook this study to determine if H-1 magnetic resonance spectroscopy (MRS) of sputum and exhaled breath condensate (EBC), as a noninvasive tool, can identify metabolic biomarkers of lung cancer. MATERIALS AND METHODS: Sputum and EBC samples were collected from 20 patients, comprising patients with pathologically confirmed non-small cell lung cancer (n = 10) and patients with benign respiratory conditions (n = 10). Both sputum and EBC samples were collected from 18 patients; 2 patients provided EBC samples only. H-1 MR spectra were obtained on a Bruker Avance 400 MHz nuclear magnetic resonance (NMR) spectrometer. Sputum samples were further confirmed cytologically to distinguish between true sputum and saliva. RESULTS: In the EBC samples, median concentrations of propionate, ethanol, acetate, and acetone were higher in lung cancer patients compared to the patients with benign conditions. Median concentration of methanol was lower in lung cancer patients (0.028 mM) than in patients with benign conditions (0.067 mM; P = 0.028). In the combined sputum and saliva and the cytologically confirmed sputum samples, median concentrations of N-acetyl sugars, glycoprotein, propionate, lysine, acetate, and formate were lower in the lung cancer patients than in patients with benign conditions. Glucose was found to be consistently absent in the combined sputum and saliva samples (88%) as well as in the cytologically confirmed sputum samples (86%) of lung cancer patients. CONCLUSION: Absence of glucose in sputum and lower concentrations of methanol in EBC of lung cancer patients discerned by H-1 MRS may serve as metabolic biomarkers of lung cancer for early detection, monitoring treatment response, and detecting recurrence.
引用
收藏
页码:29 / 35
页数:7
相关论文
共 37 条
[1]   Reduced Lung-Cancer Mortality with Low-Dose Computed Tomographic Screening [J].
Aberle, Denise R. ;
Adams, Amanda M. ;
Berg, Christine D. ;
Black, William C. ;
Clapp, Jonathan D. ;
Fagerstrom, Richard M. ;
Gareen, Ilana F. ;
Gatsonis, Constantine ;
Marcus, Pamela M. ;
Sicks, JoRean D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (05) :395-409
[2]  
Ahmed N, 2016, 24 SCI M EXH INT SOC
[3]   Benefits and Harms of CT Screening for Lung Cancer A Systematic Review [J].
Bach, Peter B. ;
Mirkin, Joshua N. ;
Oliver, Thomas K. ;
Azzoli, Christopher G. ;
Berry, Donald A. ;
Brawley, Otis W. ;
Byers, Tim ;
Colditz, Graham A. ;
Gould, Michael K. ;
Jett, James R. ;
Sabichi, Anita L. ;
Smith-Bindman, Rebecca ;
Wood, Douglas E. ;
Qaseem, Amir ;
Detterbeck, Frank C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2012, 307 (22) :2418-2429
[4]   Noninvasive detection of lung cancer by analysis of exhaled breath [J].
Bajtarevic, Amel ;
Ager, Clemens ;
Pienz, Martin ;
Klieber, Martin ;
Schwarz, Konrad ;
Ligor, Magdalena ;
Ligor, Tomasz ;
Filipiak, Wojciech ;
Denz, Hubert ;
Fiegl, Michael ;
Hilbe, Wolfgang ;
Weiss, Wolfgang ;
Lukas, Peter ;
Jamnig, Herbert ;
Hackl, Martin ;
Haidenberger, Alfred ;
Buszewski, Boguslaw ;
Miekisch, Wolfram ;
Schubert, Jochen ;
Amann, Anton .
BMC CANCER, 2009, 9 :348
[5]  
Bezabeh T, 2012, J ANAL ONCOL, V1, P14, DOI DOI 10.6000/1927-7229.2012.01.01.3
[6]   Cancer Cell Metabolism [J].
Cairns, R. A. ;
Harris, I. ;
McCracken, S. ;
Mak, T. W. .
METABOLISM AND DISEASE, 2011, 76 :299-311
[7]   Cancer Cell Metabolism: One Hallmark, Many Faces [J].
Cantor, Jason R. ;
Sabatini, David M. .
CANCER DISCOVERY, 2012, 2 (10) :881-898
[8]  
Gadian D.G., 1982, NUCL MAGNETIC RESONA
[9]   c-Myc suppression of miR-23a/b enhances mitochondrial glutaminase expression and glutamine metabolism [J].
Gao, Ping ;
Tchernyshyov, Irina ;
Chang, Tsung-Cheng ;
Lee, Yun-Sil ;
Kita, Kayoko ;
Ochi, Takafumi ;
Zeller, Karen I. ;
De Marzo, Angelo M. ;
Van Eyk, Jennifer E. ;
Mendell, Joshua T. ;
Dang, Chi V. .
NATURE, 2009, 458 (7239) :762-U100
[10]   Causes and consequences of increased glucose metabolism of cancers [J].
Gillies, Robert J. ;
Robey, Ian ;
Gatenby, Robert A. .
JOURNAL OF NUCLEAR MEDICINE, 2008, 49 :24S-42S