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Novel aminopeptidase N (APN/CD13) inhibitor 24F can suppress invasion of hepatocellular carcinoma cells as well as angiogenesis.

Abstract
Aminopeptidase N (APN)/CD13 is a widely expressed transmembrane protein and its altered expression has been detected in various cancer cells. Several APN inhibitors have been developed and some of them have been found to have effectiveness as anti-cancer agents. This article reports anti-cancer effects of a hydroxamic acid derivative 24F that was newly-synthesized as an APN inhibitor. 24F had the ability to inhibit the invasion of hepatocellular carcinoma (HCC) cell line HuH-7, although the growth of HuH-7 was not significantly inhibited at the analyzed concentrations of 24F and incubation times used. Furthermore, incubation of vascular endothelial cells with 24F was found to be effective for the suppression of the angiogenic phenomenon. These results suggest that the novel APN inhibitor 24F may work as an anti-cancer agent for HCC via inhibition of HCC cell invasion and angiogenesis.
AuthorsYoshinori Inagaki, Wei Tang, Li Zhang, Guanhua Du, Wenfang Xu, Norihiro Kokudo
JournalBioscience trends (Biosci Trends) Vol. 4 Issue 2 Pg. 56-60 (Apr 2010) ISSN: 1881-7823 [Electronic] Japan
PMID20448342 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Hydroxamic Acids
  • CD13 Antigens
Topics
  • Antineoplastic Agents (chemistry, pharmacology, therapeutic use)
  • CD13 Antigens (antagonists & inhibitors)
  • Carcinoma, Hepatocellular (drug therapy)
  • Cell Line, Tumor
  • Endothelial Cells (drug effects)
  • Humans
  • Hydroxamic Acids (chemistry, pharmacology, therapeutic use)
  • Liver Neoplasms (drug therapy)
  • Molecular Structure
  • Neoplasm Invasiveness (prevention & control)
  • Neovascularization, Pathologic (prevention & control)

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