New MDR modulators and apoptosis inducers from Euphorbia species.

Anticancer Res

Department of Medical Microbiology and Immunobiology, Faculty of Medicine, University of Szeged, Hungary.

Published: November 2007

AI Article Synopsis

  • Several macrocyclic diterpenes were extracted from Hungarian Euphorbia species and tested for their ability to reverse multidrug resistance (MDR) in colon cancer cells.
  • Among these, Compound 8 showed the highest activity, working synergistically with the chemotherapy drug epirubicin.
  • The most effective derivative was also able to induce moderate apoptosis in various cancer cell lines, suggesting these natural compounds could lead to new treatments for overcoming MDR in cancer therapy.

Article Abstract

Several macrocyclic diterpenes with jatrophane or lathyrane skeletons were isolated from methanol extracts of Hungarian Euphorbia species and evaluated for multidrug resistance (MDR)-reversing activity on a human colon cancer cell line. MDR-reversing activity was tested by using a standard functional assay with Rhodamine 123 as a fluorescent substrate analogue of epirubicin. In the model of combination chemotherapy, the interactions between epirubicin and certain resistance modifiers were studied in vitro. Compound 8 proved to be the most active, exhibiting a synergistic interaction. The capacity of the most effective derivative to induce apoptosis was demonstrated by flow cytometric analysis and by staining with ethidium bromide and acridine orange, using human mdrl gene-transfected mouse lymphoma cells and a human cervical adenocarcinoma cell line. The selected diterpene was able to induce moderate apoptosis in the tested cell lines. The data presented here indicate that naturally occurring Euphorbia diterpenes can be regarded as effective lead compounds for the reversal of MDR.

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