Association of vascular endothelial growth factor (VEGF) Gene polymorphisms and expression with the risk of endometriosis: a case–control study

• Published in: Molecular biology reports 2019-06, Vol.46 (3), p.3445-3450
• Main Authors: Rashidi, Batool Hossein, Sarhangi, Negar, Aminimoghaddam, Soheila, Haghollahi, Fedyeh, Naji, Tahereh, Amoli, Mahsa M., Shahrabi-Farahani, Maryam
• Format: Article
• Language: English
• Subjects: Adult; Angiogenesis; Animal Anatomy; Animal Biochemistry; Biomedical and Life Sciences; Case-Control Studies; Diagnosis; Endometriosis; Endometriosis - genetics; Endometriosis - metabolism; Endometrium; Endometrium - metabolism; Female; Gene expression; Gene Frequency; Gene polymorphism; Genetic Predisposition to Disease; Genotype; Genotyping; Gynecology; Histology; Humans; Life Sciences; Menstrual cycle; Middle Aged; Morphology; Neovascularization, Pathologic - genetics; Original Article; Polymerase chain reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Population studies; Restriction fragment length polymorphism; Risk Factors; Surgery; Transcriptome; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A - genetics; Vascular Endothelial Growth Factor A - metabolism
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-019-04807-6

Endometriosis is a polygenic and multifactorial gynecology situation which might be associated with angiogenesis. In the current study we assess the role of vascular endothelial growth factor (VEGF) − 2578 A/C, and + 936 C/T polymorphisms in susceptibility to endometriosis and checking the expression of VEGF mRNA in eutopic tissue of endometrium with and without endometriosis. The study was comprised of 300 patients who underwent laparascopic or laparotomy surgery with 100 cases who had confirmed histological diagnosis of endometriosis, and 200 controls with no histological diagnosis of disease. The genotyping of VEGF polymorphisms was done by polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) technique and the gene expression in tissue was determined using Real-Time PCR assay. There was no important difference of allele distribution of the − 2578 A/C (P = 0.7) and + 936 C/T (P = 0.5) polymorphisms among endometriosis cases and controls. Study of VEGF expression during the menstrual cycle, showed that endometrial tissue in cases group expressed more VEGF mRNA at the secretory phase compared to the proliferative phase (P = 0.03). Our results suggest that − 2578 A/C and + 936 C/T polymorphisms of VEGF did not seem to have impact on endometriosis predisposition in our study population. Also we did not find any link between VEGF mRNA expression and risk of endometriosis.