Gakubunkan Institute of Physiology and Medicine, Jobu University, 270-1 Shinmachi, Takasaki, Gunma 370-1393, Japan.
J Biochem. 2013 Jan;153(1):13-9. doi: 10.1093/jb/mvs136. Epub 2012 Nov 21.
Vascular endothelial growth factors (VEGFs) belong to the platelet-derived growth factor supergene family, and they play central roles in the regulation of angiogenesis and lymphangiogenesis. VEGF-A, the major factor for angiogenesis, binds to two tyrosine kinase (TK) receptors, VEGFR-1 (Flt-1) and VEGFR-2 (KDR/Flk-1), and regulates endothelial cell proliferation, migration, vascular permeability, secretion and other endothelial functions. VEGFR-2 exhibits a strong TK activity towards pro-angiogenic signals, whereas the soluble VEGFR-1 (sFlt-1) functions as an endogenous VEGF inhibitor. sFlt-1 is abnormally overexpressed in the placenta of preeclampsia patients, resulting in the major symptoms of the disease due to abnormal trapping of VEGFs. The VEGF-VEGFR system is crucial for tumour angiogenesis, and anti-VEGF-VEGFR molecules are now widely used in the clinical field to treat cancer patients. The efficacy of these molecules in prolonging the overall survival of patients has been established; however, some cancers do not respond well and reduced tumour sensitivity to anti-VEGF signals may occur after long-term treatment. The molecular basis of tumour refractoriness should be determined to improve anti-angiogenic therapy.
血管内皮生长因子(VEGF)属于血小板衍生生长因子超家族,在调节血管生成和淋巴管生成中起核心作用。血管生成的主要因子 VEGF-A 与两种酪氨酸激酶(TK)受体 VEGFR-1(Flt-1)和 VEGFR-2(KDR/Flk-1)结合,并调节内皮细胞的增殖、迁移、血管通透性、分泌和其他内皮功能。VEGFR-2 对促血管生成信号具有很强的 TK 活性,而可溶性 VEGFR-1(sFlt-1)作为内源性 VEGF 抑制剂发挥作用。子痫前期患者胎盘中超表达 sFlt-1,导致疾病的主要症状,因为 VEGFs 的异常捕获。VEGF-VEGFR 系统对肿瘤血管生成至关重要,抗 VEGF-VEGFR 分子现已广泛应用于临床领域,用于治疗癌症患者。这些分子在延长患者总生存期方面的疗效已得到证实;然而,一些癌症反应不佳,并且在长期治疗后,肿瘤对抗 VEGF 信号的敏感性可能降低。应确定肿瘤耐药的分子基础,以改善抗血管生成治疗。