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The Relation of VEGFA, VEGFR2, VEGI, and HIF1A Genetic Variants and Their Serum Protein Levels with Breast Cancer in Egyptian Patients

乳腺癌 生物 基因型 HIF1A型 血管生成 血管内皮生长因子A 内科学 血管内皮生长因子 癌症 基因分型 癌症研究 肿瘤科 等位基因 医学 遗传学 血管内皮生长因子受体 基因
作者
Amani A. Abdelgalil,Rehan Monir,Mohamed Elmetwally,Maivel H. Ghattas,Fagr B. Bazeed,Noha M. Mesbah,Dina Mohamed Abo–Elmatty,Eman T. Mehanna
出处
期刊:Biochemical Genetics [Springer Science+Business Media]
卷期号:62 (1): 547-573 被引量:3
标识
DOI:10.1007/s10528-023-10419-4
摘要

Abstract Breast cancer is the most common type of cancer in Egyptian females. Polymorphisms in the angiogenesis pathway have been implicated previously in cancer risk and prognosis. The aim of the current study was to determine whether certain polymorphisms in the genes of vascular endothelial growth factor A (VEGFA), vascular endothelial growth factor receptor 2 (VEGFR2), vascular endothelial growth inhibitor (VEGI), and hypoxia-inducible factor-1α (HIF1A) associated with breast cancer development. The study included 154 breast cancer patients and 132 apparently healthy age-matched females as a control group. VEGFA rs25648 genotyping was performed using (ARMS) PCR technique; while VEGFR2 rs2071559, VEGI rs6478106, and HIF-1α rs11549465 were genotyped by the PCR-RFLP method. Serum levels of VEGF, VEGFR2, VEGI, and HIF1A proteins in breast cancer patients and controls were measured by ELISA. There was a significant association between the VEGFA rs25648 C allele and breast cancer risk (OR = 2.5, 95% CI = 1.7–3.6, p < 0.001). VEGFA rs25648 C/C genotype was statistically significantly higher in breast cancer patients vs. control (p < 0.001). Participants with the T/T and T/C VEGFR2 rs2071559 genotypes had 5.46 and 5 higher odds, respectively, of having breast cancer than those with the C/C genotype. For the VEGI rs6478106 polymorphism, there was a higher proportion of C allele in breast cancer patients vs. control (P = 0.003). Moreover, the C/C genotype of VEGI rs6478106 was statistically significantly higher in breast cancer patients vs. control (P = 0.001). There was no significant difference in genotypes and allele frequencies of HIF-1A rs11549465 polymorphism between breast cancer cases and control individuals (P > 0.05). Serum levels of VEGFA, VEGI, and HIF1A were considerably greater in women with breast cancer than in the control (P < 0.001). In conclusion, the genetic variants VEGFA rs25648, VEGFR2 rs2071559, and VEGI rs6478106 revealed a significant association with increased breast cancer risk in Egyptian patients.
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