Early diagnosis of bladder cancer through the detection of urinary tyrosine-phosphorylated proteins

被引:13
|
作者
Khadjavi, A. [1 ]
Mannu, F. [2 ]
Destefanis, P. [3 ]
Sacerdote, C. [4 ,5 ]
Battaglia, A. [3 ]
Allasia, M. [3 ]
Fontana, D. [3 ]
Frea, B. [3 ]
Polidoro, S. [6 ,7 ]
Fiorito, G. [6 ,7 ]
Matullo, G. [6 ,7 ]
Pantaleo, A. [8 ]
Notarpietro, A. [9 ]
Prato, M. [1 ]
Castagno, F. [10 ]
Vineis, P. [11 ]
Gontero, P. [3 ]
Giribaldi, G. [9 ]
Turrini, F. [9 ]
机构
[1] Univ Turin, Dept Neurosci, I-10126 Turin, Italy
[2] Nurex Srl, Sassari, Italy
[3] Univ Turin, Dept Surg Sci, Hosp San Giovanni Battista, Urol Clin Citta Salute & Sci Torino, I-10126 Turin, Italy
[4] Univ Turin, Dept Med Sci, Unit Canc Epidemiol, I-10126 Turin, Italy
[5] Ctr Canc Epidemiol & Prevent CPO Piemonte, Turin, Italy
[6] Univ Turin, HuGeF Human Genet Fdn, I-10126 Turin, Italy
[7] Univ Turin, Dept Med Sci, I-10126 Turin, Italy
[8] Univ Sassari, Dept Biomed Sci, I-07100 Sassari, Italy
[9] Univ Turin, Sch Med, Dept Oncol, I-10126 Turin, Italy
[10] Hosp San Giovanni Battista, Blood Ctr AO Citta Salute & Sci Torino, Turin, Italy
[11] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, MRC PHE Ctr Environm & Hlth, London, England
关键词
bladder cancer; urinary tyrosine-phosphorylated proteins; urinary tumour markers; diagnostic assay; 5-AMINOLEVULINIC ACID; MARKERS; IDENTIFICATION; FLUORESCENCE; ASSAY;
D O I
10.1038/bjc.2015.232
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A noninvasive, highly sensitive and specific urine test is needed for bladder cancer (BC) diagnosis and surveillance in addition to the invasive cystoscopy. We previously described the diagnostic effectiveness of urinary tyrosine-phosphorylated proteins (UPY) and a new assay (UPY-A) for their measurement in a pilot study. The aim of this work was to evaluate the performances of the UPY-A using an independent cohort of 262 subjects. Methods: Urinary tyrosine-phosphorylated proteins were measured by UPY-A test. The area under ROC curve, cutoff, sensitivity, specificity and predictive values of UPY-A were determined. The association of UPY levels with tumour staging, grading, recurrence and progression risk was analysed by Kruskal-Wallis and Wilcoxon's test. To test the probability to be a case if positive at the UPY-A, a logistic test adjusted for possible confounding factor was used. Results: Results showed a significant difference of UPY levels between patients with BC vs healthy controls. For the best cutoff value, 261.26 Standard Units (SU), the sensitivity of the assay was 80.43% and the specificity was 78.82%. A statistically significant difference was found in the levels of UPY at different BC stages and grades between Ta and T1 and with different risk of recurrence and progression. A statistically significant increased risk for BC at UPY-A >= 261.26 SU was observed. Conclusions: The present study supplies important information on the diagnostic characteristics of UPY-A revealing remarkable performances for early stages and allowing its potential use for different applications encompassing the screening of high-risk subjects, primary diagnosis and posttreatment surveillance.
引用
收藏
页码:469 / 475
页数:7
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