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Inhibitory effects of a novel marine terpenoid on sensitive and multidrug resistant KB cell lines.

Abstract
Mechanisms of growth inhibition by the novel marine compound dehydrothyrsiferol (DHT) were investigated in a sensitive and an MDR+ human epidermoid cancer cell line. DHT was found to circumvent multidrug resistance mediated by P-glycoprotein. Cell cycle analysis revealed an accumulation in S-phase. The anchorage independent clonogenic growth in soft agar was not significantly reduced at IC50 concentrations. Reduced cell growth caused by induction of apoptotic or necrotic cell death could not be verified. Therefore, cell proliferation during an incubation period of five days was measured and found to be significantly reduced. We conclude that growth inhibition by dehydrothyrsiferol in KB cancer cells is not mediated by apoptosis but by growth retardation; the reasons for this are worth being investigated in detail.
AuthorsM K Pec, M Hellan, K Moser-Thier, J J Fernández, M L Souto, E Kubista
JournalAnticancer research (Anticancer Res) 1998 Jul-Aug Vol. 18 Issue 4C Pg. 3027-32 ISSN: 0250-7005 [Print] Greece
PMID9713504 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antineoplastic Agents, Phytogenic
  • Pyrans
  • Terpenes
  • dehydrothyrsiferol
Topics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 (metabolism)
  • Antineoplastic Agents, Phytogenic (pharmacology)
  • Apoptosis (drug effects)
  • Cell Adhesion (drug effects)
  • Cell Cycle (drug effects)
  • Cell Division (drug effects)
  • Drug Resistance, Multiple
  • Humans
  • KB Cells
  • Necrosis
  • Pyrans (pharmacology)
  • Sensitivity and Specificity
  • Terpenes (pharmacology)

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