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In vitro and in vivo reversal of cancer cell multidrug resistance by 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone.

Abstract
2',4'-Dihydroxy-6'-methoxy-3',5'-dimethylchalcone (DMC) isolated from the buds of Cleistocalyx operculatus, was investigated for its reversal effects on cancer cell multidrug resistance. DMC potentiated the cytotoxicity of the chemotherapeutic agent doxorubicin to drug-resistant KB-A1 cells. When 5 microM DMC was present simultaneously with doxorubicin, the IC50 of DOX on KB-A1 cells decreased from 13.9 +/- 0.7 microg/ml to 3.6 +/- 0.7 microg/ml. A human carcinoma xenograft model was established with the KB-A1 cell line. DMC could sensitize the tumors to doxorubicin as indicated by a considerable reduction in tumor weight. DMC increased the intracellular accumulation of doxorubicin in KB-A1 cells. When KB-A1 cells were exposed to 10 microg/ml doxorubicin combined with 5, 10, 20 microM DMC for 4 hours, the intracellular concentrations of doxorubicin were increased 1.4-, 1.8-, 3.1-fold, respectively, in comparison with doxorubicin alone treatment. All results indicated that DMC had reversal effects on the multidrug resistance phenotype.
AuthorsF Qian, C L Ye, D Z Wei, Y H Lu, S L Yang
JournalJournal of chemotherapy (Florence, Italy) (J Chemother) Vol. 17 Issue 3 Pg. 309-14 (Jun 2005) ISSN: 1120-009X [Print] England
PMID16038525 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antibiotics, Antineoplastic
  • Chalcones
  • Chalcone
  • Doxorubicin
Topics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 (biosynthesis)
  • Animals
  • Antibiotics, Antineoplastic (pharmacology)
  • Carcinoma (drug therapy, veterinary)
  • Chalcone (analogs & derivatives, pharmacology)
  • Chalcones
  • Doxorubicin (pharmacology)
  • Drug Resistance, Multiple
  • Gene Expression Profiling
  • Humans
  • Mice
  • Mice, Nude
  • Mouth Neoplasms (drug therapy, veterinary)
  • Myrtaceae (chemistry)
  • Polymerase Chain Reaction
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

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