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Fusicoccin-A selectively induces apoptosis in tumor cells after interferon-alpha priming.

Abstract
Active small molecules have a high potential for the development into new anti-cancer drugs. Here we analysed the effect of the natural occurring fusicoccanes, Fusicoccin-A (FC), Ophiobolin-A (OPH-A) and Ophiobolin-I (OPH-I) on various tumor cell lines. Both FC and OPH-A inhibit tumor cell growth efficiently, in contrast to OPH-I. Further analysis showed that FC is tumor specific, and that its efficacy can be enhanced by combining it with the cytokine interferon-alpha (IFN-alpha). In this, IFN-alpha primes the tumor cells for apoptosis induction by FC, in which DR4 and the TRAIL pathway plays an important role. Healthy cells (HUVECs, Human Umbilical Vein Endothelial Cells) are far less sensitive to IFN-alpha/FC treatment and need the continuous presence of both compounds in order to achieve a growth reduction. This differential response between healthy and tumor cells indicates that the IFN-alpha/FC treatment is a promising new cancer treatment, especially when IFN-alpha and FC are used sequentially.
AuthorsIngrid J de Vries-van Leeuwen, Chantal Kortekaas-Thijssen, Jean A Nzigou Mandouckou, Sjors Kas, Antonio Evidente, Albertus H de Boer
JournalCancer letters (Cancer Lett) Vol. 293 Issue 2 Pg. 198-206 (Jul 28 2010) ISSN: 1872-7980 [Electronic] Ireland
PMID20153922 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2010 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • Glycosides
  • Interferon-alpha
  • Sesterterpenes
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • ophiobolins
  • fusicoccin
Topics
  • Antineoplastic Agents (pharmacology)
  • Antineoplastic Combined Chemotherapy Protocols (pharmacology)
  • Apoptosis (drug effects)
  • Cell Line
  • Cell Line, Tumor
  • Glycosides (pharmacology)
  • Humans
  • Interferon-alpha (pharmacology)
  • Sesterterpenes (pharmacology)
  • TNF-Related Apoptosis-Inducing Ligand (metabolism)

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