Selective cancer cell cytotoxicity from exposure to dihydroartemisinin and holotransferrin

Cancer Lett. 1995 May 4;91(1):41-6. doi: 10.1016/0304-3835(94)03716-v.

Abstract

Rapid cell death, as evidenced by a decrease in cell counts, was observed when molt-4-lymphoblastoid cells, a human leukemia cell line, were exposed to holotransferrin (12 microM) and dihydroartemisinin (1-200 microM). Incubation with either compound alone was significantly less effective. Significantly less cell death was observed when normal human lymphocytes were exposed to a combination of these 2 drugs. Probit analysis of dose-response functions shows that the drug combination is approximately 100 times more effective on molt-4 cells than lymphocytes (LD50s for molt-4 and lymphocytes were 2.59 microM and 230 microM, respectively). This drug combination may provide a novel approach for cancer treatment.

MeSH terms

  • Artemisinins*
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • Drug Combinations
  • Humans
  • Lymphocytes / drug effects*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Sesquiterpenes
  • Time Factors
  • Transferrin / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Artemisinins
  • Drug Combinations
  • Sesquiterpenes
  • Transferrin
  • holotransferrin
  • artenimol