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Inhibitory effects of Yangzheng Xiaoji on angiogenesis and the role of the focal adhesion kinase pathway

机译:养正消肌对血管生成的抑制作用及黏着斑激酶途径的作用

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摘要

Angiogenesis is an essential event during the excessive growth and metastatic spread of solid tumours. Anti-angiogenic agents have become a new choice of therapy for patients with cancer. In the present study, we investigated the potential effect of Yangzheng Xiaoji, a traditional Chinese medicinal formula presently used in the treatment of several solid tumours including liver cancer and gastric cancer, on angiogenesis, in vitro. The human vascular endothelial cell line HECV was used. A Matrigel-based sandwich tubule formation assay was employed to assess in vitro angiogenesis, a colorimetric method for assessing in vitro cell growth. Electric cell-substrate impedance sensing (ECIS) was used to evaluate the adhesion and migration of endothelial cells. The effects on activation of focal adhesion kinase (FAK) were evaluated using western blotting and immunofluorescence methods. Yangzhen Xiaoji extract DME25 significantly inhibited tube formation (p=0.046 vs control). This was seen together with a concentration-dependent inhibition on cell-matrix adhesion and cellular migration. It was demonstrated that the focal adhesion kinase (FAK) inhibitor PF557328 had a significant synergistic effect on DME25-induced inhibition of cell adhesion, migration and tube formation. The study showed that DME25 inhibited the phosphorylation of FAK in endothelial cells. In conclusion, Yangzhen Xiaoji has a marked effect on angiogenesis, in vitro and that this effect is at least partly mediated by the focal adhesion kinase (FAK) pathway.
机译:在实体瘤的过度生长和转移性扩散期间,血管生成是必不可少的事件。抗血管生成剂已成为癌症患者治疗的新选择。在本研究中,我们调查了目前正用于治疗包括肝癌和胃癌在内的多种实体瘤的中药配方“正证小结”在体外对血管生成的潜在作用。使用人血管内皮细胞系HECV。基于基质胶的三明治小管形成试验用于评估体外血管生成,这是一种用于评估体外细胞生长的比色法。电细胞-基底阻抗感测(ECIS)用于评估内皮细胞的粘附和迁移。使用蛋白质印迹和免疫荧光方法评估对粘着斑激酶(FAK)激活的影响。养珍小蓟提取物DME25显着抑制管形成(与对照组相比,p = 0.046)。可以看到这与浓度依赖性的细胞基质粘附和细胞迁移抑制有关。结果表明,粘着斑激酶(FAK)抑制剂PF557328对DME25诱导的细胞粘附,迁移和管形成的抑制具有显着的协同作用。研究表明DME25抑制了内皮细胞中FAK的磷酸化。总之,养真小肌在体外具有显着的血管生成作用,并且这种作用至少部分是由粘着斑激酶(FAK)途径介导的。

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