Unusual cellular uptake of cytotoxic 4-hydroxymethyl-3-aminoacridine

Eur J Med Chem. 2009 Nov;44(11):4758-63. doi: 10.1016/j.ejmech.2009.06.034. Epub 2009 Jul 4.

Abstract

Aminoacridine derivatives display interesting chemical and biological properties in the field of antitumor agents. The synthesis of 4-hydroxymethyl-3-aminoacridine and its iodo labelled analogue allows the study of cell distribution using two innovative, complementary and powerful techniques, real time fluorescence microscopy and dynamic secondary ion mass spectrometry (SIMS). All the data point to lysosomal localization of the active molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acridines / pharmacokinetics*
  • Acridines / pharmacology
  • Antineoplastic Agents / pharmacokinetics*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Membrane Permeability
  • Cell Proliferation / drug effects
  • Humans
  • Lysosomes / metabolism*
  • Microscopy, Fluorescence
  • Spectrometry, Mass, Secondary Ion

Substances

  • 4-hydroxymethyl-3-aminoacridine
  • Acridines
  • Antineoplastic Agents