Growth inhibition by tyrosine kinase inhibitors in mesothelioma cell lines.

J.E. Nutt, K. O'Toole, D. Gonzalez, J. Lunec

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

Clinical outcome following chemotherapy for malignant pleural mesothelioma is poor and improvements are needed. This preclinical study investigates the effect of five tyrosine kinase inhibitors (PTK787, ZD6474, ZD1839, SU6668 and SU11248) on the growth of three mesothelioma cell lines (NCI H226, NCI H28 and MSTO 211H), the presence of growth factor receptors and inhibition of their downstream signalling pathways. GI50 values were determined: ZD6474 and SU11248, mainly VEGFR2 inhibitors, gave the lowest GI50 across all cell lines (3.5-6.9 microM) whereas ZD1839 gave a GI50 in this range only in H28 cells. All cell lines were positive for EGFR, but only H226 cells were positive for VEGFR2 by Western blotting. ZD6474 and ZD1839 inhibited EGF-induced phosphorylation of EGFR, AKT and ERK, whereas VEGF-induced phosphorylation of VEGFR2 was completely inhibited with 0.1 microM SU11248. VEGFR2 was detected in tumour samples by immunohistochemistry. VEGFR2 tyrosine kinase inhibitors warrant further investigation in mesothelioma.
Original languageEnglish
Pages (from-to)1684-1691
Number of pages8
JournalEuropean Journal of Cancer
Volume45
Issue number9
DOIs
Publication statusPublished - Jun 2009

Keywords

  • Antineoplastic Agents
  • Blotting, Western
  • Cell Division
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Humans
  • Mesothelioma
  • Neoplasm Proteins
  • Phosphorylation
  • Protein Kinase Inhibitors
  • Protein-Tyrosine Kinases
  • Receptor, Epidermal Growth Factor
  • Tumor Cells, Cultured
  • Vascular Endothelial Growth Factor Receptor-2

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