Paneling human thyroid cancer cell lines for candidate proteins for targeted anti-angiogenic therapy

✍ Scribed by Sebastian Hoffmann; Anette Wunderlich; Ilhan Celik; Katja Maschuw; Iyad Hassan; Lorenz C. Hofbauer; Andreas Zielke

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 264 KB
• Volume: 98
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.20832

✦ Synopsis

Abstract

Tumor angiogenesis is believed to result from an imbalance of pro‐ and anti‐angiogenic factors, some of which are candidates for targeted therapy. Such therapy has raised hopes for patients with undifferentiated thyroid carcinomas, who are facing a grave prognosis with a survival of only months. In this study, in vivo growth of xenografted human thyroid carcinomas unexpectedly responded quite differently to neutralizing anti‐vascular endothelial growth factor (VEGF) antibody. In particular, lasting inhibition as well as accelerated growth occurred after treatment. Consequently, a panel of anti‐angiogenic factors was addressed in a representative sample of thyroid carcinoma lines. VEGF, fibroblast growth factor (FGF‐2), and endostatin were demonstrated by Western blotting and EIA, whereas PDGF‐A, PDGF‐B, and IL‐6 were negative. Quantification of VEGF, FGF‐2, and endostatin revealed a wide range of concentrations from 500 to 4,200 pg/ml VEGF, 5 to 60 pg/ml FGF‐2, and 50 to 300 pg/ml endostatin, not related to a particular histologic thyroid carcinoma background. Angiostatin (kringles 1–3) was detected in all, but one of the cell lines. Finally, aaATIII was confirmed in FTC133 cells. These data highlight the complex regulation of angiogenesis in thyroid carcinoma cell lines and suggest that the array of angiogenic factors differs markedly between individual cell lines. For the first time, angiostatin, endostatin, and possibly also aaATIII are identified as novel candidate regulators of angiogenesis in thyroid carcinoma cells. J. Cell. Biochem. 98: 954–965, 2006. © 2006 Wiley‐Liss, Inc.