Urinary proteomics and metabolomics studies to monitor bladder health and urological diseases

被引:30
作者
Chen, Zhaohui [1 ]
Kim, Jayoung [2 ,3 ,4 ]
机构
[1] Cedars Sinai Med Ctr, Adv Clin Biosyst Res Inst, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Surg, 8700 Beverly Blvd, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Dept Biomed Sci, 8700 Beverly Blvd, Los Angeles, CA 90048 USA
[4] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
基金
美国国家卫生研究院;
关键词
Urinary biomarkers; Proteomics; Metabolomics; Bladder diseases; PROTEIN BIOMARKER DISCOVERY; MAPP RESEARCH NETWORK; PROSTATE-CANCER; EXTRACELLULAR VESICLES; LUNG-CANCER; ANTIPROLIFERATIVE FACTOR; INTERSTITIAL CYSTITIS; LC-MS; CE-MS; IDENTIFICATION;
D O I
10.1186/s12894-016-0129-7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Assays of molecular biomarkers in urine are non-invasive compared to other body fluids and can be easily repeated. Based on the hypothesis that the secreted markers from the diseased organs may locally release into the body fluid in the vicinity of the injury, urine-based assays have been considered beneficial to monitoring bladder health and urological diseases. The urine proteome is much less complex than the serum and tissues, but nevertheless can contain biomarkers for diagnosis and prognosis of diseases. The urine metabolome has a much higher number and concentration of low-molecular metabolites than the serum or tissues, with a far lower lipid concentration, yet informs directly about dietary and microbial metabolism. Discussion: We here discuss the use of mass spectrometry-based proteomics and metabolomics for urine biomarker assays, specifically with respect to the underlying mechanisms that trigger the pathological condition. Conclusion: Molecular biomarker profiles, based on proteomics and metabolomics studies, reliably distinguish patients from healthy controls, stratify sub-populations with respect to treatment options, and predict therapeutic response of patients with urological disease.
引用
收藏
页数:13
相关论文
共 126 条
[41]   Proteomic methods for biomarker discovery and validation. Are we there yet? [J].
Hathout, Yetrib .
EXPERT REVIEW OF PROTEOMICS, 2015, 12 (04) :329-331
[42]   Screening for Prostate Cancer With the Prostate-Specific Antigen Test A Review of Current Evidence [J].
Hayes, Julia H. ;
Barry, Michael J. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2014, 311 (11) :1143-1149
[43]   CE-ESI-MS for bottom-up proteomics: Advances in separation, interfacing and applications [J].
Heemskerk, Anthonius A. M. ;
Deelder, Andre M. ;
Mayboroda, Oleg A. .
MASS SPECTROMETRY REVIEWS, 2016, 35 (02) :259-271
[44]   Proteomics in clinical prostate research [J].
Hellstrom, Magnus ;
Jonmarker, Sara ;
Lehtio, Janne ;
Auer, Gert ;
Egevad, Lars .
PROTEOMICS CLINICAL APPLICATIONS, 2007, 1 (09) :1058-1065
[45]   Urinary biomarkers for prostate cancer: a review [J].
Hessels, Daphne ;
Schalken, Jack A. .
ASIAN JOURNAL OF ANDROLOGY, 2013, 15 (03) :333-339
[46]  
Hiemstra Thomas F, 2011, J Biomol Tech, V22, P136
[47]   Diagnostic potential for urinary proteomics [J].
Hortin, Glen L. ;
Sviridov, Denis .
PHARMACOGENOMICS, 2007, 8 (03) :237-255
[48]   Lipid signalling in plant responses to abiotic stress [J].
Hou, Quancan ;
Ufer, Guido ;
Bartels, Dorothea .
PLANT CELL AND ENVIRONMENT, 2016, 39 (05) :1029-1048
[49]   Analytical challenges translating mass spectrometry-based phosphoproteomics from discovery to clinical applications [J].
Iliuk, Anton B. ;
Arrington, Justine V. ;
Tao, Weiguo Andy .
ELECTROPHORESIS, 2014, 35 (24) :3430-3440
[50]   Novel non-invasive biomarkers that distinguish between benign prostate hyperplasia and prostate cancer [J].
Jedinak, Andrej ;
Curatolo, Adam ;
Zurakowski, David ;
Dillon, Simon ;
Bhasin, Manoj K. ;
Libermann, Towia A. ;
Roy, Roopali ;
Sachdev, Monisha ;
Loughlin, Kevin R. ;
Moses, Marsha A. .
BMC CANCER, 2015, 15