Department of Medicine and Vascular Biology Center, Augusta University, Augusta, GA, USA.
Expert Opin Ther Targets. 2021 May;25(5):381-391. doi: 10.1080/14728222.2021.1940139. Epub 2021 Jun 17.
: Vascular endothelial growth factor (VEGF)-A is a sought therapeutic target for PAD treatment because of its potent role in angiogenesis. However, no therapeutic benefit was achieved in VEGF-A clinical trials, suggesting that our understanding of VEGF-A biology and ischemic angiogenic processes needs development. Alternate splicing in VEGF-A produces pro- and anti-angiogenic VEGF-A isoforms; the only difference being a 6-amino acid switch in the C-terminus of the final 8th exon of the gene. This finding has changed our understanding of VEGF-A biology and may explain the lack of benefit in VEGF-A clinical trials. It presents new therapeutic opportunities for peripheral arterial disease (PAD) treatment.: Literature search was conducted to include: 1) predicted mechanism by which the anti-angiogenic VEGF-A isoform would inhibit angiogenesis, 2) unexpected mechanism of action, and 3) how this mechanism revealed novel signaling pathways that may enhance future therapeutics in PAD.: Inhibiting a specific anti-angiogenic VEGF-A isoform in ischemic muscle promotes perfusion recovery in preclinical PAD. Additional efforts focused on the production of these isoforms, and the pathways altered by modulating different VEGF receptor-ligand interactions, and how this new data may allow bedside progress offers new approaches to PAD are discussed.I.
血管内皮生长因子(VEGF)-A 是治疗 PAD 的治疗靶点,因为它在血管生成中具有强大的作用。然而,在 VEGF-A 临床试验中并未取得治疗效果,这表明我们对 VEGF-A 生物学和缺血性血管生成过程的理解需要进一步发展。VEGF-A 的选择性剪接产生了促血管生成和抗血管生成的 VEGF-A 异构体;唯一的区别是基因最后第 8 个外显子的 C 末端有 6 个氨基酸的转换。这一发现改变了我们对 VEGF-A 生物学的理解,并可能解释了 VEGF-A 临床试验中缺乏疗效的原因。它为外周动脉疾病(PAD)的治疗提供了新的治疗机会。
进行了文献检索,包括:1)抗血管生成 VEGF-A 异构体抑制血管生成的预测机制,2)意想不到的作用机制,以及 3)这种机制揭示了哪些新的信号通路可能增强 PAD 的未来治疗效果。
在缺血性肌肉中抑制特定的抗血管生成 VEGF-A 异构体可促进临床前 PAD 中的灌注恢复。额外的研究集中在这些异构体的产生,以及通过调节不同的 VEGF 受体-配体相互作用改变的途径,以及这些新数据如何使床边进展成为可能,讨论了为 PAD 提供的新方法。