Prognostic value of serum Tie-2 and vascular endothelial growth factor levels in cancer patients

M.M. Seker, E. Sancaktar, D.O. Acibucu, A.K. Filiz, K. Deveci, A. Bahceci, T. Kacan, N. Babacan, S. Yuce

Department of Medical Oncology, Department of Biochemistry, Department of Physiology, Department of Ear & Nose & Throat, Cumhuriyet University Faculty of Medicine, Sivas, Turkey. mmetinseker@yahoo.com.tr

 

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• Oncology

BACKGROUND: Angiogenesis is a very essential process in tumor biology. Vascular endothelial growth factor (VEGF), angiopoietin and its receptor (TIE-2) are very important mediators for angiogenesis. In this trial, we aimed to analyze the role of these mediators on chemotherapy response and survival.

PATIENTS AND METHODS: Forty four cancer patients and 22 healthy controls were included in the study. Baseline serum samples were obtained from all participants and post-chemotherapy serum samples were obtained from the cancer patients. Serum vascular endothelial growth factor and TIE-2 levels were measured with quantitative enzyme-linked immunosorbent assay techniques.

RESULTS: The baseline serum vascular endothelial growth factor level was 187.5 and 120.2 pg/ml in cancer patients and the control group (p = 0.006). The baseline serum TIE-2 level was 615.9 and 242.5 pg/ml in the patients and control group (p < 0.001). There was a significant difference between patients’ baseline and post-chemotherapy VEGF levels (111.9 pg/ml; p < 0.001) and patients’ baseline and post-chemotherapy TIE-2 levels (344.5 pg/ml; p < 0.001). The overall survival rate was better in patients who had lower baseline VEGF and TIE-2 levels and whose TIE-2 level had decreased with chemotherapy.

CONCLUSIONS: Higher baseline TIE-2 and VEGF levels are related and worsen survival. Decreasing levels of TIE-2, but not VEGF, which, with chemotherapy, may be predictive for survival.

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