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Angiopoietin-2 Is Implicated in the Regulation of Tumor Angiogenesis

机译:Angiopoietin-2参与肿瘤血管生成的调控。

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摘要

We addressed the effect of angiopoietin expression on tumor growth and metastasis. Overexpression of angiopoietin-2 (Ang-2) in Lewis lung carcinoma and TA3 mammary carcinoma cells inhibited their ability to form metastatic tumors and prolonged the survival of mice injected with the corresponding transfectants. In contrast, angiopoietin-1 (Ang-1) overexpression had no detectable effect on the ability of either tumor type to disseminate. Tumors derived from Ang-2-overexpressing cells displayed aberrant angiogenic vessels that took the form of vascular cords or aggregated vascular endothelial cells with few associated smooth muscle cells. These vascular cords or aggregates were accompanied by endothelial and tumor cell apoptosis, suggesting that an imbalance in Ang-2 expression with respect to Ang-1 and vascular endothelial growth factor may disrupt angiogenesis and tumor survival in vivo. Our observations suggest that Ang-2 may play an important role in regulating tumor angiogenesis.
机译:我们研究了血管生成素表达对肿瘤生长和转移的影响。 Lewis肺癌和TA3乳腺癌细胞中血管生成素2(Ang-2)的过表达抑制了它们形成转移性肿瘤的能力,并延长了注射相应转染子的小鼠的生存期。相反,血管生成素-1(Ang-1)的过表达对这两种肿瘤的扩散能力均没有可检测的影响。源自Ang-2过表达细胞的肿瘤表现出异常的血管生成血管,呈血管束或聚集的血管内皮细胞的形式,很少有相关的平滑肌细胞。这些血管索或聚集体伴随着内皮细胞和肿瘤细胞凋亡,表明相对于Ang-1和血管内皮生长因子而言,Ang-2表达的失衡可能破坏体内血管生成和肿瘤存活。我们的观察结果表明,Ang-2可能在调节肿瘤血管生成中起重要作用。

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