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Proteolytic Cleavages in the VEGF Family: Generating Diversity among Angiogenic VEGFs Essential for the Activation of Lymphangiogenic VEGFs

机译:VEGF家族中的蛋白水解裂解:在血管生成VEGF之间产生多样性对淋巴管源性VEGF的激活是必不可少的

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摘要

Vascular endothelial growth factors (VEGFs) regulate the growth of blood and lymphatic vessels. Some of them induce the growth of blood vessels, and others the growth of lymphatic vessels. Blocking VEGF-A is used today to treat several types of cancer (“antiangiogenic therapy”). However, in other diseases, we would like to increase the activity of VEGFs. For example, VEGF-A could generate new blood vessels to protect from heart disease, and VEGF-C could generate new lymphatics to counteract lymphedema. Clinical trials are testing the latter concept at the moment. Because VEGF-C and VEGF-D are produced as inactive precursors, we propose that novel drugs could also target the enzymatic activation of VEGF-C and VEGF-D. However, because of the delicate balance between too much and too little vascular growth, a detailed understanding of the activation of the VEGFs is needed before such concepts can be converted into safe and efficacious therapies.
机译:血管内皮生长因子(VEGFS)调节血液和淋巴管的生长。其中一些诱导血管的生长,以及其他淋巴血管的生长。今天使用阻止VEGF-A来治疗几种类型的癌症(“抗血管生成疗法”)。然而,在其他疾病中,我们想增加VEGF的活动。例如,VEGF-A可以产生新的血管以保护免受心脏病,而VEGF-C可以产生新的淋巴管来抵消淋巴水肿。临床试验目前正在测试后一种概念。因为VEGF-C和VEGF-D作为非活性前体,我们提出了新的药物还可以靶向VEGF-C和VEGF-D的酶活化。然而,由于血管生长太多和太少之间的微妙平衡,在这种概念转换成安全和有效的疗法之前,需要对VEGF激活的详细了解。

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