Urine-Based Metabolomics and Machine Learning Reveals Metabolites Associated with Renal Cell Carcinoma Stage

Simple Summary Every year, hundreds of thousands of cases of renal carcinoma (RCC) are reported worldwide. Accurate staging of the disease is important for treatment and prognosis purposes; however, contemporary methods such as computerized tomography (CT) and biopsies are expensive and prone to sampling errors, respectively. As such, a non-invasive diagnostic assay for staging would be beneficial. This study aims to investigate urine metabolites as potential biomarkers to stage RCC using machine learning techniques to mine the complex datasets produced. We present a 24-metabolite panel that discriminates between early stage and advanced stage RCC with 87% accuracy in our study cohort. Abstract Urine metabolomics profiling has potential for non-invasive RCC staging, in addition to providing metabolic insights into disease progression. In this study, we utilized liquid chromatography-mass spectrometry (LC-MS), nuclear magnetic resonance (NMR), and machine learning (ML) for the discovery of urine metabolites associated with RCC progression. Two machine learning questions were posed in the study: Binary classification into early RCC (stage I and II) and advanced RCC stages (stage III and IV), and RCC tumor size estimation through regression analysis. A total of 82 RCC patients with known tumor size and metabolomic measurements were used for the regression task, and 70 RCC patients with complete tumor-nodes-metastasis (TNM) staging information were used for the classification tasks under ten-fold cross-validation conditions. A voting ensemble regression model consisting of elastic net, ridge, and support vector regressor predicted RCC tumor size with a R2 value of 0.58. A voting classifier model consisting of random forest, support vector machines, logistic regression, and adaptive boosting yielded an AUC of 0.96 and an accuracy of 87%. Some identified metabolites associated with renal cell carcinoma progression included 4-guanidinobutanoic acid, 7-aminomethyl-7-carbaguanine, 3-hydroxyanthranilic acid, lysyl-glycine, glycine, citrate, and pyruvate. Overall, we identified a urine metabolic phenotype associated with renal cell carcinoma stage, exploring the promise of a urine-based metabolomic assay for staging this disease.

[1]  T. Ruman,et al.  Serum and urine analysis with gold nanoparticle-assisted laser desorption/ionization mass spectrometry for renal cell carcinoma metabolic biomarkers discovery. , 2021, Advances in medical sciences.

[2]  David L. Roberts,et al.  Machine Learning-Enabled Renal Cell Carcinoma Status Prediction Using Multiplatform Urine-Based Metabolomics. , 2021, Journal of proteome research.

[3]  A. Jemal,et al.  Cancer Statistics, 2021 , 2021, CA: a cancer journal for clinicians.

[4]  Jie He,et al.  Enhanced expression of queuine tRNA-ribosyltransferase 1 (QTRT1) predicts poor prognosis in lung adenocarcinoma , 2020, Annals of translational medicine.

[5]  P. Beauseroy,et al.  Coupled Mass-Spectrometry-Based Lipidomics Machine Learning Approach for Early Detection of Clear Cell Renal Cell Carcinoma. , 2020, Journal of proteome research.

[6]  V. Copié,et al.  Nuclear magnetic resonance and surface-assisted laser desorption/ionization mass spectrometry-based metabolome profiling of urine samples from kidney cancer patients. , 2020, Journal of pharmaceutical and biomedical analysis.

[7]  Kwanjeera Wanichthanarak,et al.  Deep metabolome: Applications of deep learning in metabolomics , 2020, Computational and structural biotechnology journal.

[8]  Lars M Blank,et al.  Machine Learning Applications for Mass Spectrometry-Based Metabolomics , 2020, Metabolites.

[9]  A. Mohammed,et al.  Epidemiology of Renal Cell Carcinoma , 2020, World journal of oncology.

[10]  A. Brazma,et al.  Dysregulation at multiple points of the kynurenine pathway is a ubiquitous feature of renal cancer: implications for tumour immune evasion , 2020, British Journal of Cancer.

[11]  Ana Margarida Araújo,et al.  Volatilomics Reveals Potential Biomarkers for Identification of Renal Cell Carcinoma: An In Vitro Approach , 2020, Metabolites.

[12]  B. Faubert,et al.  Metabolic reprogramming and cancer progression , 2020, Science.

[13]  T. Pan,et al.  tRNA Queuosine Modification Enzyme Modulates the Growth and Microbiome Recruitment to Breast Tumors , 2020, Cancers.

[14]  J. Zahiri,et al.  Digging deeper into volatile organic compounds associated with cancer , 2019, Biology methods & protocols.

[15]  J. Moscat,et al.  The complexity of the serine glycine one-carbon pathway in cancer , 2019, The Journal of cell biology.

[16]  H. Vogel,et al.  Urinary Metabolomics Validates Metabolic Differentiation Between Renal Cell Carcinoma Stages and Reveals a Unique Metabolic Profile for Oncocytomas , 2019, Metabolites.

[17]  X. Liu,et al.  Urine Metabolomics for Renal Cell Carcinoma (RCC) Prediction: Tryptophan Metabolism as an Important Pathway in RCC , 2019, Front. Oncol..

[18]  Saifur R Khan,et al.  Unbiased data analytic strategies to improve biomarker discovery in precision medicine. , 2019, Drug discovery today.

[19]  I. Ben-Sahra,et al.  Cancer Cells Tune the Signaling Pathways to Empower de Novo Synthesis of Nucleotides , 2019, Cancers.

[20]  Yanhong Zhou,et al.  Crucial role of the pentose phosphate pathway in malignant tumors. , 2019, Oncology letters.

[21]  R. Henrique,et al.  The Complex Interplay between Metabolic Reprogramming and Epigenetic Alterations in Renal Cell Carcinoma , 2019, Genes.

[22]  C. Porta,et al.  Renal cell carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†. , 2019, Annals of oncology : official journal of the European Society for Medical Oncology.

[23]  Stefano Nembrini,et al.  The revival of the Gini importance? , 2018, Bioinform..

[24]  Jia-ju Lv,et al.  Overexpression of ATP citrate lyase in renal cell carcinoma tissues and its effect on the human renal carcinoma cells in vitro , 2018, Oncology letters.

[25]  Miroslava Cuperlovic-Culf,et al.  Machine Learning Methods for Analysis of Metabolic Data and Metabolic Pathway Modeling , 2018, Metabolites.

[26]  R. Weiss,et al.  Metabolic reprogramming in clear cell renal cell carcinoma , 2017, Nature Reviews Nephrology.

[27]  A. Badawy Kynurenine Pathway of Tryptophan Metabolism: Regulatory and Functional Aspects , 2017, International journal of tryptophan research : IJTR.

[28]  Mark W. Ball,et al.  Urine and Serum Metabolomics Analyses May Distinguish between Stages of Renal Cell Carcinoma , 2017, Metabolites.

[29]  F. Schena,et al.  Renal Cell Carcinoma: A Study through NMR-Based Metabolomics Combined with Transcriptomics , 2016, Diseases.

[30]  Chris Sander,et al.  An Integrated Metabolic Atlas of Clear Cell Renal Cell Carcinoma. , 2016, Cancer cell.

[31]  Eoin Fahy,et al.  Metabolomics Workbench: An international repository for metabolomics data and metadata, metabolite standards, protocols, tutorials and training, and analysis tools , 2015, Nucleic Acids Res..

[32]  W. Linehan,et al.  Aerobic glycolysis: a novel target in kidney cancer , 2013, Expert review of anticancer therapy.

[33]  Christian M. Metallo,et al.  Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells , 2013, Nature.

[34]  D. Vitkup,et al.  Heterogeneity of tumor-induced gene expression changes in the human metabolic network , 2013, Nature Biotechnology.

[35]  R. Gilbert,et al.  Structure and physicochemical properties of octenyl succinic anhydride modified starches: a review. , 2013, Carbohydrate polymers.

[36]  V. Mootha,et al.  Metabolite Profiling Identifies a Key Role for Glycine in Rapid Cancer Cell Proliferation , 2012, Science.

[37]  P. Robson,et al.  Glycine Decarboxylase Activity Drives Non-Small Cell Lung Cancer Tumor-Initiating Cells and Tumorigenesis , 2012, Cell.

[38]  Laurent Poulain,et al.  Understanding the central role of citrate in the metabolism of cancer cells. , 2012, Biochimica et biophysica acta.

[39]  Z. Bhujwalla,et al.  Choline metabolism in malignant transformation , 2011, Nature Reviews Cancer.

[40]  Masaaki Komatsu,et al.  Autophagy: Renovation of Cells and Tissues , 2011, Cell.

[41]  O. Nalcioglu,et al.  Clinical characteristics and biomarkers of breast cancer associated with choline concentration measured by 1H MRS , 2011, NMR in biomedicine.

[42]  Gaël Varoquaux,et al.  The NumPy Array: A Structure for Efficient Numerical Computation , 2011, Computing in Science & Engineering.

[43]  Gaël Varoquaux,et al.  Scikit-learn: Machine Learning in Python , 2011, J. Mach. Learn. Res..

[44]  Heinz-Peter Schlemmer,et al.  Discriminating Cancer From Noncancer Tissue in the Prostate by 3-Dimensional Proton Magnetic Resonance Spectroscopic Imaging: A Prospective Multicenter Validation Study , 2011, Investigative radiology.

[45]  Geng-yin Zhou,et al.  Noninvasive evaluation of cerebral glioma grade by using multivoxel 3D proton MR spectroscopy. , 2011, Magnetic resonance imaging.

[46]  Skipper Seabold,et al.  Statsmodels: Econometric and Statistical Modeling with Python , 2010, SciPy.

[47]  Wes McKinney,et al.  Data Structures for Statistical Computing in Python , 2010, SciPy.

[48]  L. Cantley,et al.  Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation , 2009, Science.

[49]  John D. Hunter,et al.  Matplotlib: A 2D Graphics Environment , 2007, Computing in Science & Engineering.

[50]  Brian E. Granger,et al.  IPython: A System for Interactive Scientific Computing , 2007, Computing in Science & Engineering.

[51]  Travis E. Oliphant,et al.  Python for Scientific Computing , 2007, Computing in Science & Engineering.

[52]  Mitchel S Berger,et al.  Correlation of magnetic resonance spectroscopic and growth characteristics within Grades II and III gliomas. , 2007, Journal of neurosurgery.

[53]  O. Herbarth,et al.  Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control , 2006, British Journal of Cancer.

[54]  Y. Jaiswal,et al.  Hypomodification of Transfer RNA in Cancer with Respect to Queuosine , 2005, RNA biology.

[55]  Raymond Vanholder,et al.  Review on uremic toxins: classification, concentration, and interindividual variability. , 2003, Kidney international.

[56]  U. Grohmann,et al.  T cell apoptosis by tryptophan catabolism , 2002, Cell Death and Differentiation.

[57]  J. Jakowicki,et al.  Deficiency of queuine, a highly modified purine base, in transfer RNAs from primary and metastatic ovarian malignant tumors in women. , 1994, Cancer research.

[58]  H. Kersten,et al.  Relationship of queuine-lacking transfer RNA to the grade of malignancy in human leukemias and lymphomas. , 1985, Cancer research.

[59]  H. Peters,et al.  The excretion of 3-hydroxyanthranilic acid in patients with bladder and kidney carcinoma. , 1975, Acta vitaminologica et enzymologica.

[60]  S. Nishimura,et al.  Possible anticodon sequences of tRNA His , tRNA Asm , and tRNA Asp from Escherichia coli B. Universal presence of nucleoside Q in the first postion of the anticondons of these transfer ribonucleic acids. , 1972, Biochemistry.