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Effects of a multikinase inhibitor motesanib (AMG 706) alone and combined with the selective DuP-697 COX-2 inhibitor on colorectal cancer cells

  • Tijen Temiz Kaya
  • , Ahmet Altun
  • , Nergiz Hacer Turgut*
  • , Hilmi Ataseven
  • , Gokhan Koyluoglu
  • *Corresponding author for this work
  • Cumhuriyet University

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

In the present study, we investigated the effects of motesanib (AMG 706), a multikinase inhibitor alone and in combination with DuP-697, an irreversible selective inhibitor of COX-2, on cell proliferation, angiogenesis, and apoptosis induction in a human colorectal cancer cell line (HT29). Real time cell analysis (RTCA, Xcelligence system) was used to determine the effects on colorectal cancer cell proliferation. Apoptosis was assessed with annexin V staining and angiogenesis was determined with chorioallantoic membrane model. We found that motesanib alone exerted antiproliferative, antiangiogenic and apoptotic effects on HT29 colorectal cancer cells. Combination with DUP-697 increased the antiproliferative, antiangiogenic and apoptotic effects. Results of this study indicate that motesanib may be a good choice in treatment of colorectal tumors. In addition, the increased effects of combination of motesanib with DuP-697 raise the possibility of using lower doses of these drugs and therefore avoid/minimize the dose-dependent side effects generally observed.

Original languageEnglish
Pages (from-to)1103-1110
Number of pages8
JournalAsian Pacific Journal of Cancer Prevention
Volume17
Issue number3
DOIs
StatePublished - 19 Apr 2016
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • COX-2 inhibition
  • Colorectal cancer
  • Motesanib
  • Multikinase inhibitor

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