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阳正消积对血管生成的抑制作用及粘着斑激酶通路的作用。

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

机构信息

Metastasis and Angiogenesis Research Group, Cardiff University School of Medicine, Heath Park, Cardiff CF14 4XN, UK.

出版信息

Int J Oncol. 2012 Nov;41(5):1635-42. doi: 10.3892/ijo.2012.1627. Epub 2012 Sep 11.

DOI:10.3892/ijo.2012.1627
PMID:22971748
Abstract

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.

摘要

血管生成是实体瘤过度生长和转移扩散的一个必要事件。抗血管生成药物已成为癌症患者治疗的新选择。在本研究中,我们研究了养正消积,一种目前用于治疗肝癌和胃癌等多种实体瘤的中药配方,对血管生成的潜在影响,在体外。我们使用人血管内皮细胞系 HECV。采用基于 Matrigel 的三明治管状形成测定法评估体外血管生成,采用比色法评估体外细胞生长。采用电动细胞-底物阻抗传感(ECIS)评估内皮细胞的黏附和迁移。使用 Western blot 和免疫荧光方法评估对粘着斑激酶(FAK)激活的影响。养正消积提取物 DME25 显著抑制管形成(p=0.046 与对照相比)。这与细胞-基质黏附的浓度依赖性抑制和细胞迁移一起观察到。研究表明,粘着斑激酶(FAK)抑制剂 PF557328 对 DME25 诱导的细胞黏附、迁移和管形成抑制具有显著协同作用。研究表明,DME25 抑制内皮细胞中 FAK 的磷酸化。总之,养正消积对血管生成具有显著作用,体外至少部分是通过粘着斑激酶(FAK)途径介导的。

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