Anti-tumor and anti-angiogenic effects in mice of heparin conjugated to angiostatic steroids

E. J. Derbyshire, G. A. Comin, Y. C. Yang, J. Overholser, L. Watkins, P. E. Thorpe

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Abstract

Heparin-steroid conjugates have been prepared by linking a non-anti-coagulating derivative of heparin, which binds to endothelial cells, to an angiostatic steroid, which suppresses endothelial cell division. One such conjugate, heparin adipic hydrazide (HAH) linked to cortisol, has previously been shown to inhibit both angiogenesis and the growth of solid tumors in mice. In the present study, heparin hydrazide (HH) was linked to tetrahydro S, tetrahydrocortisone and tetrahydrocortisol, which are devoid of glucocorticoid and mineralocorticold activity and hence were predicted to have low toxicity to animals. The tetrahydro steroid conjugates were compared with the cortisol conjugate for therapeutic effectiveness against solid Lewis lung carcinoma growing in mice. HAH-cortisol reduced tumor growth by up to 75% whereas a simple mixture of HAH and cortisol was not significantly inhibitory. In contrast to HAH-cortisol, the 3 tetrahydro steroid conjugates did not significantly inhibit tumor growth. The differences in anti-tumor properties of the conjugates correlated with their ability to inhibit angiogenesis in a Matrigel implant model in mice. The tetrahydro steroid conjugates did not significantly inhibit angiogenesis whereas HAH-cortisol inhibited angiogenesis by greater than 90%. Therefore, HAH-cortisol is the most effective heparin-steroid conjugate so far developed.

Original languageEnglish (US)
Pages (from-to)694-701
Number of pages8
JournalInternational Journal of Cancer
Volume63
Issue number5
DOIs
Publication statusPublished - 1995

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ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Derbyshire, E. J., Comin, G. A., Yang, Y. C., Overholser, J., Watkins, L., & Thorpe, P. E. (1995). Anti-tumor and anti-angiogenic effects in mice of heparin conjugated to angiostatic steroids. International Journal of Cancer, 63(5), 694-701. https://doi.org/10.1002/ijc.2910630515