Graduate Program in Immunology, Department of Immunology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Department of Physiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Mol Med Rep. 2014 Mar;9(3):1044-8. doi: 10.3892/mmr.2014.1890. Epub 2014 Jan 9.
Vascular endothelial growth factor (VEGF) is one of the key modulators of angiogenesis. The highly polymorphic promoter and 5' untranslated region of VEGF have been associated with susceptibility to and aggressiveness of several types of cancer. To examine the functional role of VEGF polymorphisms at -634 and -1498 positions, VEGF mRNA and protein in breast cancer tissues were analyzed by quantitative polymerase chain reaction and immunohistochemistry. A dual-luciferase assay was performed to determine promoter activity. The VEGF-634CC genotype demonstrated the highest VEGF mRNA expression. High VEGF mRNA expression was correlated with a tumor size of >2 cm, the presence of lymphovascular invasion and the presence of axillary nodal metastasis. The promoter containing the -1,498T/-634C haplotype exhibited the highest basal promoter activity. These findings suggest that the interaction between -1,498T and -634C polymorphisms increases VEGF expression and is involved in breast cancer aggressiveness.
血管内皮生长因子(VEGF)是血管生成的关键调节剂之一。VEGF 的高度多态性启动子和 5'非翻译区与多种类型癌症的易感性和侵袭性有关。为了研究 VEGF 多态性在-634 和-1498 位置的功能作用,通过定量聚合酶链反应和免疫组织化学分析乳腺癌组织中的 VEGF mRNA 和蛋白。进行双荧光素酶测定以确定启动子活性。VEGF-634CC 基因型表现出最高的 VEGF mRNA 表达。高 VEGF mRNA 表达与肿瘤大小>2cm、存在淋巴血管侵犯和腋窝淋巴结转移有关。含有-1,498T/-634C 单倍型的启动子表现出最高的基础启动子活性。这些发现表明,-1,498T 和-634C 多态性之间的相互作用增加了 VEGF 的表达,并参与了乳腺癌的侵袭性。