University of Pittsburgh, Cancer Institute and Department of Medicine, HCCLB, 2.19, 5117 Centre Avenue; Pittsburgh, PA 15213, USA.
Mol Cancer Ther. 2010 Apr;9(4):929-41. doi: 10.1158/1535-7163.MCT-09-0953. Epub 2010 Apr 6.
Epidermal growth factor receptor (EGFR) vIII is a mutated EGFR that is frequently overexpressed in glioblastomas and implicated in response to receptor tyrosine kinase inhibitors. In this study, we investigate the effect of ZD6474 (ZACTIMA, vandetanib), a dual inhibitor for vascular endothelial growth factor receptor 2 and EGFR on growth and angiogenesis of gliomas expressing EGFRvIII. We used two glioma xenograft models, U87MG cells overexpressing EGFRvIII and short-term cultured primary glioma GBM8 cells with EGFRvIII. ZD6474 inhibited tumor growth and angiogenesis and induced cell apoptosis in various brain gliomas. Moreover, significant inhibition of EGFRvIII-expressing U87MG and GBM8 gliomas was observed compared with their controls. Magnetic resonance imaging analysis using the apparent diffusion coefficient and three-dimensional T2*weighed measurements validated ZD6474 inhibition on tumor growth and angiogenesis in EGFRvIII-expressing GBM8 gliomas. Mechanistically, ZD6474 shows better inhibition of cell growth and survival of U87MG/EGFRvIII, GBM6, and GBM8 cells that express EGFRvIII than U87MG or GBM14 cells that have nondetectable EGFRvIII through attenuation of activated phosphorylation of signal transducer and activator of transcription 3, Akt, and Bcl-X(L) expression. Albeit in lesser extent, ZD6474 also displays suppressions of U87MG/EGFR and GBM12 cells that overexpress wild-type EGFR. Additionally, ZD6474 inhibits activation of extracellular signal-regulated kinase 1/2 in both types of cells, and expression of a constitutively active phosphoinositide 3-kinases partially rescued ZD6474 inhibition in U87MG/EGFRvIII cells. Taken together, these data show that ZD6474 significantly inhibited growth and angiogenesis of gliomas expressing EGFRvIII by specifically blocking EGFRvIII-activated signaling mediators, suggesting a potential application of ZD6474 in treatments for glioblastomas that overexpress EGFRvIII. Mol Cancer Ther; 9(4); 929-41. (c)2010 AACR.
表皮生长因子受体 (EGFR) vIII 是一种突变的 EGFR,在胶质母细胞瘤中频繁过表达,并与受体酪氨酸激酶抑制剂的反应有关。在这项研究中,我们研究了血管内皮生长因子受体 2 和 EGFR 的双重抑制剂 ZD6474(ZACTIMA,凡德他尼)对表达 EGFRvIII 的胶质瘤生长和血管生成的影响。我们使用了两种神经胶质瘤异种移植模型,过表达 EGFRvIII 的 U87MG 细胞和短期培养的具有 EGFRvIII 的原发性神经胶质瘤 GBM8 细胞。ZD6474 抑制了各种脑胶质瘤的肿瘤生长和血管生成,并诱导了细胞凋亡。此外,与对照相比,观察到对表达 EGFRvIII 的 U87MG 和 GBM8 神经胶质瘤的显著抑制。使用表观扩散系数和三维 T2*加权测量的磁共振成像分析验证了 ZD6474 在表达 EGFRvIII 的 GBM8 神经胶质瘤中的肿瘤生长和血管生成抑制作用。从机制上讲,ZD6474 通过减弱信号转导和转录激活因子 3、Akt 和 Bcl-X(L)表达的激活磷酸化,对表达 EGFRvIII 的 U87MG/EGFRvIII、GBM6 和 GBM8 细胞的生长和存活表现出更好的抑制作用,而 U87MG 或 GBM14 细胞则没有检测到 EGFRvIII。尽管程度较小,但 ZD6474 也显示出对过表达野生型 EGFR 的 U87MG/EGFR 和 GBM12 细胞的抑制作用。此外,ZD6474 抑制两种类型细胞中细胞外信号调节激酶 1/2 的激活,并且组成性激活的磷酸肌醇 3-激酶的表达部分挽救了 U87MG/EGFRvIII 细胞中 ZD6474 的抑制作用。总之,这些数据表明,ZD6474 通过特异性阻断 EGFRvIII 激活的信号转导介质,显著抑制表达 EGFRvIII 的神经胶质瘤的生长和血管生成,提示 ZD6474 在治疗过表达 EGFRvIII 的胶质母细胞瘤方面具有潜在应用。 Mol Cancer Ther; 9(4); 929-41. (c)2010 AACR.