Improved effect of an antiangiogenic tyrosine kinase inhibitor (SU5416) by combinations with fractionated radiotherapy or low molecular weight heparin

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Lund, Eva Løbner
  • Minna W.B. Olsen
  • Kenneth E. Lipson
  • Gerald McMahon
  • Anthony R. Howlett
  • Paul E.G. Kristjansen

The effect of combining SU5416 with fractionated radiotherapy or with low molecular weight (LMW) heparin (dalteparin) was studied in U87 human glioblastoma xenografts in nude mice. SU5416 is antiangiogenic by a specific inhibition of the vascular endothelial growth factor receptor 2 (VEGFR-2), and heparins are assumed to bind VEGF. Both SU5416 (100 mg/kg every second day in 5 days) and 3 Gy × 5 produced moderate, yet significant, growth inhibition. Tumors treated with concomitant irradiation and short-term SU5416 maintained a lower growth rate during regrowth than the other treatment groups (P=.007). Dalteparin (1000 IE/kg subcutaneously once a day) had no growth-inhibitory effect on its own, but when this LMW heparin was added to the SU5416 schedule, a significantly enhanced growth inhibition was obtained. VEGF protein content in tumors was not significantly altered by SU5416, but a significant decrease in VEGF levels was found in tumors treated with concomitant dalteparin and SU5416 compared with controls (P=.03). We conclude that: 1) an additive growth-inhibitory effect is obtained by combining SU5416 and fractionated radiotherapy; and 2) LMW heparin (dalteparin), in combination with SU5416, decreases the level of VEGF in tumors and increases the growth-inhibitory effect of SU5416.

OriginalsprogEngelsk
TidsskriftNeoPlasia
Vol/bind5
Udgave nummer2
Sider (fra-til)155-160
Antal sider6
ISSN1522-8002
DOI
StatusUdgivet - 2003

Bibliografisk note

Funding Information:
Address all correspondence to: Paul E. G. Kristjansen, MD, PhD, Molecular Pathology, University of Copenhagen, Frederik V’s Vej 11, Copenhagen DK - 2100, Denmark. E - mail: paulk@pai.ku.dk 1The work was supported by grant 101 0016 9132 from the Danish Cancer Society, grant 5701 from the Danish Cancer Research Foundation, and a grant from the Faculty of Health Sciences, University of Copenhagen. Received 19 April 2002; Revised 8 January 2003; Accepted 9 January 2003.

ID: 288186409