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Abolished angiogenicity and tumorigenicity of rat glioma by 1-naphthalenemonosulfonate.

Abstract
Suramins and suradistas, an important group of potential anti-cancer agents, inhibit fibroblast growth factor (FGF) mitogenic activity. It has been shown that naphthalenesulfonates, with a common chemical function to the family of suramins and suradistas, mimic their inhibitory activity, abolishing FGF-induced angiogenesis in vivo, and inducing apoptosis of C6 glioma cells in culture. In the present report, we show that intratumoral administration of 1-naphthalenemonosulfonate induces a considerable regression of gliomas in rats, significantly enhances apoptosis, and attenuates tumor angiogenesis. These findings may lead to new approaches for the treatment of glioblastoma, a most common primary malignant brain tumor of very poor prognosis, as well as of other angiogenesis-dependent malignancies.
AuthorsP Cuevas, F Carceller, D Diaz, D Reimers, M Fernández, R M Lozano, R González-Corrochano, G Giménez-Gallego
JournalNeuroscience letters (Neurosci Lett) Vol. 308 Issue 3 Pg. 185-8 (Aug 10 2001) ISSN: 0304-3940 [Print] Ireland
PMID11479019 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Angiogenesis Inhibitors
  • Antineoplastic Agents
  • Naphthalenesulfonates
  • 1-naphthalenesulfonic acid
  • Fibroblast Growth Factors
Topics
  • Angiogenesis Inhibitors (pharmacology)
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Brain Neoplasms (drug therapy)
  • Fibroblast Growth Factors (physiology)
  • Glioma (drug therapy)
  • In Situ Nick-End Labeling
  • Naphthalenesulfonates (pharmacology)
  • Neoplasm Transplantation
  • Neovascularization, Pathologic (drug therapy, physiopathology)
  • Rats
  • Rats, Sprague-Dawley
  • Tumor Cells, Cultured (transplantation)

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