Combined use of Epithelial Membrane Antigen and Nuclear Matrix Protein 52 as Sensitive Biomarkers for Detection of Bladder Cancer

Author:

Attallah Abdelfattah M.1,El-Far Mohamed2,Abdallah Sanaa O.3,El-Waseef Ahmed M.2,Omran Mohamed M.4,Abdelrazek Mohamed A.1,Attallah Ahmed A.1,Saadh Mohamed J.1,Radwan Mohamed1,El-waffaey Kholoud A.1,Abol-Enei Hassan5

Affiliation:

1. Research and Development Department, Biotechnology Research Center, New Damietta City - Egypt

2. Chemistry Department, Faculty of Science, Mansoura University, Mansoura - Egypt

3. Chemistry Department, Faculty of Science, Cairo University, Giza - Egypt

4. Chemistry Department, Faculty of Science, Helwan University, Cairo - Egypt

5. Department of Urology, Urology-Nephrology Center, Mansoura University, Mansoura - Egypt

Abstract

Background The advent of noninvasive urine-based markers as well as other novel modalities has yielded improved diagnostic accuracy. However, the new markers failed to reach higher sensitivity and specificity. We therefore evaluated the potential role of epithelial membrane antigen (EMA) and nuclear matrix protein 52 (NMP-52) singly and combined as noninvasive biomarkers for the detection of bladder cancer (BC). Methods A total of 160 individuals including 66 patients with BC, 54 patients with benign urologic disorders and 40 healthy volunteers were investigated. Urinary EMA at 130 kDa and NMP at 52 kDa were identified, purified and quantified by Western blot, electroelution and enzyme-linked immunosorbent assay (ELISA). The diagnostic performance of each biomarker and their combination were compared using area under receiver operating characteristic curves (AUC). Results Mean urinary EMA, 2.42 µg/mL, and NMP-52, 17.85 µg/mL, were significantly elevated in patients with BC compared to controls, 1.18 and 3.44 µg/mL, respectively (p<0.0001). The combined use of these markers yielded values which were increased 4.4- and 13.7-fold in the benign and malignant disease groups, respectively, with respect to the normal group. The values of EMA and NMP-52 were significantly higher in patients with higher-grade tumors than those with lower-grade tumors (p<0.0001). Moreover, this combination could predict all BC stages and grades with 0.91 AUC, 94% sensitivity and 80% specificity. Conclusions EMA and NMP-52 in combination could be promising noninvasive biomarkers for BC detection.

Publisher

SAGE Publications

Subject

Cancer Research,Clinical Biochemistry,Oncology,Pathology and Forensic Medicine

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