Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Cancer. 2012 Apr 15;118(8):2106-16. doi: 10.1002/cncr.26488. Epub 2011 Aug 25.
TC-71 Ewing sarcoma cells overexpress vascular endothelial growth factor (VEGF) with a shift from the 189 to the 165 isoform.
The effect of CAPER-α on the expression of the VEGF isoforms, tumor growth, and vessel density was analyzed after transfection of TC-71 cells with CAPER-α cDNA or siRNA.
CAPER-α correlated inversely with the VEGF(165) /VEGF(189) mRNA ratio. Up-regulation of CAPER-α resulted in decreased tumor growth, tumor vessel density, and chemotactic activity of the cell's supernatant. CAPER-α expression was regulated by EWS/FLI-1 through a protein-protein interaction.
Increased VEGF(165) expression is secondary to the down-regulation of CAPER-α by EWS/FLI-1. CAPER-α mediates alternative splicing and controls the shift from VEGF(189) to VEGF(165) .
TC-71 尤文肉瘤细胞过表达血管内皮生长因子(VEGF),其 189 亚型向 165 亚型发生转变。
用 CAPER-α cDNA 或 siRNA 转染 TC-71 细胞后,分析 CAPER-α 对 VEGF 亚型表达、肿瘤生长和血管密度的影响。
CAPER-α 与 VEGF(165)/VEGF(189)mRNA 比值呈负相关。CAPER-α 的上调导致肿瘤生长、肿瘤血管密度和细胞上清液的趋化活性降低。CAPER-α 的表达受 EWS/FLI-1 通过蛋白-蛋白相互作用调控。
EWS/FLI-1 下调 CAPER-α 导致 VEGF(165)表达增加。CAPER-α 介导可变剪接并控制 VEGF(189)向 VEGF(165)的转变。