Author/Authors :
Rezaee, Hamid Neurosurgery Department - Mashhad University of Medical Sciences, Mashhad, Iran , Abbasnia, Shadi Immunology Research Centre - Inflammation and inflammatory Diseases division - Mashhad University of Medical Sciences, Mashhad, Iran , Alenabi, Anita Department of Pathology - Shariati Hospital - Mashhad University of Medical Sciences, Mashhad, Iran , Vakili, Rosita Immunology Research Centre - Inflammation and inflammatory Diseases division - Mashhad University of Medical Sciences, Mashhad, Iran , Moheghi, Nasrin Genetic Laboratory - Qaem Hosp - Mashhad University of Medical Sciences, Mashhad, Iran , Tavakol Afshari, Jalil Immunology Research Centre - Mashhad University of Medical Sciences, Mashhad, Iran , Rezaee, Abdolrahim Immunology Research Centre - Inflammation and inflammatory Diseases division - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Background: Vascular endothelial growth factor (VEGF) is one of the primary angiogenesis regulators in
solid cancers. Brain solid tumors are life-threatening diseases in which angiogenesis is an important phase of tumor development and progression. In the present study, VEGF-A and VEGF receptor (VEGF-R1) gene
expression was evaluated in CNS brain tumors.
Methods: VEGF-A and VEGF-R1 expression was quantified using real-time PCR on fresh biopsies of 38
supratentorial brain tumors compared to 30 non-tumoral tissues. Then, the correlations were investigated with
clinic-pathological and demographic factors of the patients.
Results: PCR product sequencing confirmed the validity of qRT-PCR. Although VEGF-A and VEGF-R1
expression showed increasing trends with the progression of cell proliferation in different stages of
astrocytoma, VEGF-R1 did not meet the 95% confidence interval in other brain tumors. An increasing trend
in VEGF-A expression and a declining trend in VEGF-R1 expression from Stage I to II were observed in
meningioma. VEGF-A and VEGF-R1 expression had no significant correlation with age and gender.
Although peritumoral brain edema (PTBE) in astrocytoma was significantly associated with tumor stages,
VEGF-A and VEGF-R1 were not correlated with PTBE in meningioma and metastasis.
Conclusions: VEGF-A is a valuable factor for the prognosis of PTBE and malignancy in astrocytoma and is helpful in monitoring treatment approaches.
Keywords :
Angiogenesis , Brain edema , Brain neoplasm , Peritumoral brain , VEGF , VEGFR1