The Evaluation of Vascular Endothelial Growth Factor A (VEGFA) and VEGFR2 Receptor as Prognostic Biomarkers in Bladder Cancer

Author:

El Azzouzi Meryem12ORCID,El Ahanidi Hajar13,Hafidi Alaoui Chaimae14,Chaoui Imane1,Benbacer Laila1,Tetou Mohammed25,Hassan Ilias25,Bensaid Mounia6ORCID,Oukabli Mohamed26,Ameur Ahmed25,Al Bouzidi Abderrahmane2,Attaleb Mohammed1,El Mzibri Mohammed1ORCID

Affiliation:

1. Biology and Medical Research Unit, Centre National de l’Energie, des Sciences et des Techniques Nucléaires (CNESTEN), Rabat 10001, Morocco

2. Faculty of Medicine and Pharmacy of Rabat, Mohammed V University in Rabat, Rabat 10100, Morocco

3. Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland

4. Faculty of Sciences, Mohammed V University in Rabat, Rabat 10040, Morocco

5. Department of Urology, Mohammed V Military Teaching Hospital of Rabat, Rabat 10045, Morocco

6. Department of Pathology, Mohammed V Military Teaching Hospital of Rabat, Rabat 10045, Morocco

Abstract

Vascular endothelial growth factor (VEGF) and its receptors (VEGFR1 and VEGFR2) are the most important tissue factors involved in tumor growth and angiogenesis. The aim of this study was to evaluate the promoter mutational status of VEGFA and the expression levels of VEGFA, VEGFR1, and VEGFR2 in bladder cancer (BC) tissues and to correlate the results with the clinical–pathological parameters of BC patients. A total of 70 BC patients were recruited at the Urology Department of the Mohammed V Military Training Hospital in Rabat, Morocco. Sanger sequencing was performed to investigate the mutational status of VEGFA, and RT-QPCR was used to evaluate the expression levels of VEGFA, VEGFR1, and VEGFR2. Sequencing of the VEGFA gene promoter revealed the presence of −460T/C, −2578C/A, and −2549I/D polymorphisms, and statistical analyses showed a significant correlation between −460T/C SNP and smoking (p = 0.02). VEGFA and VEGFR2 expressions were significantly up-regulated in patients with NMIBC (p = 0.003) and MIBC (p = 0.03), respectively. Kaplan–Meier analyses showed that patients with high VEGFA expression had significantly longer disease-free survival (p = 0.014) and overall survival (p = 0.009). This study was very informative, showing the implication of VEGF alterations in BC, suggesting that VEGFA and VEGFR2 expressions could be promising biomarkers for the better management of BC.

Funder

Institut de recherche sur le cancer

Publisher

MDPI AG

Subject

Clinical Biochemistry

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