Li Ding, Finley Stacey D
Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB 140, Los Angeles, California 90089, USA.
Integr Biol (Camb). 2018 Apr 23;10(4):253-269. doi: 10.1039/c8ib00019k.
Multiple promoters and inhibitors mediate angiogenesis, the formation of new blood vessels, and these factors represent potential targets for impeding vessel growth in tumors. Vascular endothelial growth factor (VEGF) is a potent angiogenic factor targeted in anti-angiogenic cancer therapies. In addition, thrombospondin-1 (TSP1) is a major endogenous inhibitor of angiogenesis, and TSP1 mimetics are being developed as an alternative type of anti-angiogenic agent. The combination of bevacizumab, an anti-VEGF agent, and ABT-510, a TSP1 mimetic, has been tested in clinical trials to treat advanced solid tumors. However, the patients' responses are highly variable and show disappointing outcomes. To obtain mechanistic insight into the effects of this combination anti-angiogenic therapy, we have constructed a novel whole-body systems biology model including the VEGF and TSP1 reaction networks. Using this molecular-detailed model, we investigated how the combination anti-angiogenic therapy changes the amounts of pro-angiogenic and anti-angiogenic complexes in cancer patients. We particularly focus on answering the question of how the effect of the combination therapy is influenced by tumor receptor expression, one aspect of patient-to-patient variability. Overall, this model complements the clinical administration of combination anti-angiogenic therapy, highlights the role of tumor receptor variability in the heterogeneous responses to anti-angiogenic therapy, and identifies the tumor receptor profiles that correlate with a high likelihood of a positive response to the combination therapy. Our model provides novel understanding of the VEGF-TSP1 balance in cancer patients at the systems-level and could be further used to optimize combination anti-angiogenic therapy.
多种促进因子和抑制因子介导血管生成,即新血管的形成,这些因子是阻碍肿瘤血管生长的潜在靶点。血管内皮生长因子(VEGF)是抗血管生成癌症治疗中靶向的一种强效血管生成因子。此外,血小板反应蛋白-1(TSP1)是血管生成的主要内源性抑制剂,TSP1模拟物正作为一种新型抗血管生成药物进行研发。抗VEGF药物贝伐单抗和TSP1模拟物ABT-510的联合用药已在治疗晚期实体瘤的临床试验中进行了测试。然而,患者的反应差异很大,结果令人失望。为了深入了解这种联合抗血管生成治疗的作用机制,我们构建了一个包含VEGF和TSP1反应网络的新型全身系统生物学模型。利用这个分子细节模型,我们研究了联合抗血管生成治疗如何改变癌症患者体内促血管生成和抗血管生成复合物的数量。我们特别关注回答联合治疗效果如何受肿瘤受体表达影响这一问题,肿瘤受体表达是患者个体差异的一个方面。总体而言,该模型补充了联合抗血管生成治疗的临床应用,突出了肿瘤受体变异性在抗血管生成治疗异质性反应中的作用,并确定了与联合治疗阳性反应高可能性相关的肿瘤受体谱。我们的模型在系统层面为癌症患者的VEGF-TSP1平衡提供了新的认识,并可进一步用于优化联合抗血管生成治疗。