Phytomedicine
Volume 17, Issue 6 , Pages 441-448, May 2010

Antitumor activity of terpenoids against classical and atypical multidrug resistant cancer cells

  • H. Lage

      Affiliations

    • Charité Campus Mitte, Institute of Pathology, Berlin, Germany
  • ,
  • N. Duarte

      Affiliations

    • Institute for Medicines and Pharmaceutical Sciences, (iMed.UL) Faculty of Pharmacy, University of Lisbon, Av. das Forças Armadas, 1600-083 Lisbon, Portugal
  • ,
  • C. Coburger

      Affiliations

    • Charité Campus Mitte, Institute of Pathology, Berlin, Germany
    • Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany
  • ,
  • A. Hilgeroth

      Affiliations

    • Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Germany
  • ,
  • M.J.U. Ferreira

      Affiliations

    • Institute for Medicines and Pharmaceutical Sciences, (iMed.UL) Faculty of Pharmacy, University of Lisbon, Av. das Forças Armadas, 1600-083 Lisbon, Portugal
    • Corresponding Author InformationCorresponding author. Tel.: +351217946475; fax: +351217946470.

published online 17 August 2009.

Abstract 

Nineteen terpenoids, including macrocyclic diterpenes, diterpenic lactones and other polycyclic diterpenes, steroids and a triterpene isolated from the methanolic extracts of Euphorbia species, were evaluated for their potential antineoplastic activity in various human cancer cell lines that were derived from three tumor entities: gastric (EPG85-257), pancreatic (EPP85-181) and colon (HT-29) carcinomas. Furthermore, different multidrug-resistant variants of these cancer cell lines with over-expression of MDR1/P-gp or no MDR1/P-gp expression were also investigated. In parental drug-sensitive cell lines, the tested compounds showed a moderate/weak antiproliferative effect or were inactive. Most of them were found more effective in drug-resistant cells than in the parental, drug-sensitive ones, and some of them showed high antineoplastic efficacy in classical or atypical drug-resistant cells. The most active compounds were the lathyrane diterpenes latilagascenes C and D, and the diterpenic lactones 3β-acetoxy-helioscopinolide B and helioscopinolide E which exhibited high antineoplastic activities against the drug-resistant subline EPG85-257RDB derived from gastric carcinoma. In addition, the macrocyclic lathyrane diterpene jolkinol B was found to be highly effective in the multidrug-resistant variant HT-29RNOV.

Keywords: Antiproliferative, Multidrug resistance, Lathyrane diterpenes, Helioscopinolides, Terpenoids

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PII: S0944-7113(09)00189-5

doi:10.1016/j.phymed.2009.07.009

Phytomedicine
Volume 17, Issue 6 , Pages 441-448, May 2010