Antiangiogenic activity of 2-formyl-8-hydroxy-quinolinium chloride

K. H. Lam, K. K.H. Lee, S. H.L. Kok, R. S.M. Wong, F. Y. Lau, G. Y.M. Cheng, Wai Yeung Wong, S. W. Tong, K. W. Chan, R. Y.K. Chan, Cheuk On Tang, C. H. Cheng, D. K.P. Hau, Z. X. Bian, R. Gambari, C. H. Chui

Research output: Journal article publicationJournal articleAcademic researchpeer-review

4 Citations (Scopus)

Abstract

Tumour growth is closely related to the development of new blood vessels to supply oxygen and nutrients to cancer cells. Without the neovascular formation, tumour volumes cannot increase and undergo metastasis. Antiangiogenesis is one of the most promising approaches for antitumour therapy. The exploration of new antiangiogenic agents would be helpful in antitumour therapy. Quinoline is an aromatic nitrogen compound characterized by a double-ring structure which exhibits a benzene ring fused to pyridine at two adjacent carbon atoms. The high stability of quinoline makes it preferable in a variety of therapeutic and pharmaceutical applications, including antitumour treatment. This work is to examine the potential antiangiogenic activity of the synthetic compound 2-Formyl-8-hydroxy-quinolinium chloride. We found that 2-Formyl-8-hydroxy-quinolinium chloride could inhibit the growth of human umbilical vein endothelial cells in vitro. Using the diethylnitrosamine-induced hepatocarcinogenesis model, 2-Formyl-8-hydroxy-quinolinium chloride showed strong antiangiogenic activity. Furthermore, 2-Formyl-8-hydroxy-quinolinium chloride could inhibit the growth of large Hep3B xenografted tumour from the nude mice. We assume that 2-Formyl-8-hydroxy-quinolinium chloride could be a potential antiangiogenic and antitumour agent and it is worthwhile to further study its underlying working mechanism.
Original languageEnglish
Pages (from-to)145-150
Number of pages6
JournalBiomedicine and Pharmacotherapy
Volume80
DOIs
Publication statusPublished - 1 May 2016

Keywords

  • 2-Formyl-8-hydroxy-quinolinium chloride
  • Antiangiogenesis
  • Antitumour
  • Diethylnitrosamine-induced hepatocarcinogenesis
  • Hepatoma xenograft

ASJC Scopus subject areas

  • Pharmacology

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