Department of Head-Neck Otolaryngology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang Province 310003, China.
Int J Oral Maxillofac Surg. 2011 Jun;40(6):628-32. doi: 10.1016/j.ijom.2010.11.005. Epub 2010 Dec 15.
Angiopoietin-2 (Ang-2) has been identified as an important factor in tumour angiogenesis through its action in blocking the stabilizing actions of Ang-2 and leading to new tumour vessel growth in the presence of vascular endothelial growth factor (VEGF). In the authors' previous study, over-expression of Ang-2 in Tca8113 tongue tumour cells inhibited growth. The current study aims to clarify the mechanisms of Ang-2-mediated tumour growth inhibition and its role in the regulation of VEGF expression. These studies used tumours derived from Ang-2-transfected Tca8113 cells injected into nude mice. The results showed that Ang-2-transfected tumours displayed aberrant angiogenic vessels with few associated smooth muscle cells. No detectable differences in VEGF expression were observed between Ang-2-transfected and parental tumours. Tumours produced by the Ang-2 transfection also had a higher apoptosis index and lower tumour cell proliferative index than tumours in the control groups. These observations suggest that enhanced expression of Ang-2 has no effect on VEGF expression and results in tumour vessel regression and inhibition of tumour growth.
血管生成素-2 (Ang-2) 通过阻断 Ang-2 的稳定作用,促进血管内皮生长因子 (VEGF) 诱导的新肿瘤血管生成,被认为是肿瘤血管生成的重要因素。在作者之前的研究中,Tca8113 舌癌细胞中 Ang-2 的过表达抑制了肿瘤的生长。本研究旨在阐明 Ang-2 介导的肿瘤生长抑制机制及其在 VEGF 表达调控中的作用。这些研究使用 Ang-2 转染的 Tca8113 细胞注射到裸鼠中产生的肿瘤。结果表明,Ang-2 转染的肿瘤显示出异常的血管生成,很少有相关的平滑肌细胞。在 Ang-2 转染的肿瘤和亲本肿瘤之间未观察到 VEGF 表达的差异。与对照组相比,Ang-2 转染产生的肿瘤具有更高的细胞凋亡指数和更低的肿瘤细胞增殖指数。这些观察结果表明,增强的 Ang-2 表达对 VEGF 表达没有影响,导致肿瘤血管退化和肿瘤生长抑制。