首页> 外文期刊>Pathology oncology research: POR >Definition of the 'Drug-Angiogenic-Activity-Index' that allows the quantification of the positive and negative angiogenic active drugs: a study based on the chorioallantoic membrane model.
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Definition of the 'Drug-Angiogenic-Activity-Index' that allows the quantification of the positive and negative angiogenic active drugs: a study based on the chorioallantoic membrane model.

机译:“药物血管生成活性指数”的定义允许对阳性和阴性血管生成活性药物进行定量:基于绒毛膜尿囊膜模型的研究。

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Since the introduction of the angiogenic therapy by Folkman et al. in the 1970'ies many antiangiogenic drugs were identified. Only few of them are still now in clinical use. Also the Vascular Endothelial Growth Factor (VEGF), the cytokine with the highest angiogenic activity, has been identified. Its antagonist, Bevacizumab, is produced and admitted for the angiogenic therapy in first line for metastatic colorectal cancer. When we look at preclinical studies, they fail of in vivo models that define the "Drug-Angiogenic-Activity-Index" of angiogenic or antiangiogenic drugs. This work proposes a possible standardized procedure to define the "Drug Angiogenic Activity Index" by counting the vascular intersections (VIS) on the Chorioallantoic Membrane after drug application. The equation was defined as follows: {DeltaVIS[Drug]-DeltaVIS[Control]} / Delta VIS[Control]. For VEGF a Drug-Angiogenic-Activity-Index of 0.92 was found and for Bevacizumab a -1. This means almost that double of the naturally angiogenic activity was achieved by VEGF on the Chorioallantoic membrane. A complete blocking of naturally angiogenic activity was observed after Bevacizumabs application. Establishing the "Drug-Angiogenic-Activity-Index" in the preclinical phase will give us an impact of effectiveness for the new constructed antiangiogenic drugs like the impact of effectiveness in the cortisone family.
机译:自从Folkman等人引入血管生成疗法以来。在1970年代,发现了许多抗血管生成药物。现在只有少数几个仍在临床上使用。还已经鉴定出血管内皮生长因子(VEGF),具有最高血管生成活性的细胞因子。生产其拮抗剂贝伐单抗,并将其用于转移性结直肠癌的一线血管生成治疗。当我们观察临床前研究时,它们无法定义定义血管生成或抗血管生成药物的“药物-血管生成活性指数”的体内模型。这项工作提出了一种可能的标准化程序,通过在药物应用后计数绒膜尿囊膜上的血管交叉点(VIS)来定义“药物血管生成活性指数”。该方程式定义如下:{DeltaVIS [药物] -DeltaVIS [对照]} / Delta VIS [对照]。对于VEGF,发现的药物-血管生成活性指数为0.92,对于贝伐单抗为-1。这意味着,血管绒毛膜上的VEGF几乎实现了自然血管生成活性的两倍。贝伐单抗应用后观察到完全阻断了天然血管生成活性。在临床前阶段建立“药物-血管生成活性指数”将使我们对新型抗血管生成药物的功效产生影响,例如对可的松家族的功效产生影响。

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