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Successful mafosfamide purging of bone marrow from chronic myelogenous leukemia (CML) cells.

Abstract
The in vitro sensitivity of human chronic myeloid leukemia-blast crisis and chronic phase (CML-BC and CML-CP, respectively) cells as well as adherent cell-depleted, T lymphocyte-depleted normal bone marrow cells (A-T-NBMC) to various concentrations of mafosfamide (ASTA Z7654), was examined by colony formation assay in the presence of IL-3 and GM-CSF, to test the possibility of purging of BMC from CML cells. Colony formation by CML cells was inhibited more efficiently than by NBMC. After the incubation with 50 micrograms/ml or 100 micrograms/ml of mafosfamide, the growth of leukemic CFU-GM was totally abrogated in 2/11 or 9/11 cases of CML-BC and in 1/7 or 6/7 cases of CML-CP, respectively. At the same time the CFU-GM arising from normal BMC were not inhibited totally with 50 or 100 micrograms/ml of the drug in any of five experiments. CML cells were still unable to form secondary colonies, while normal BMC were capable of regrowth. The CD34+ cells isolated form CML-BC and CML-CP patients were also more susceptible to mafosfamide cytotoxicity in comparison to CD34+ cells derived from NBMC. To confirm the possibility of purging, CML-BC cells were mixed with NBMC (1:1) and incubated with mafosfamide. Finally, the growing colonies were examined for the presence of bcr/abl hybrid gene by reverse transcriptase-Taq polymerase chain reaction (RT-PCR) and specific hybridization. The bcr/abl gene was not detected in the colonies growing after 100 micrograms/ml, and the signal was diminished after incubation with 50 micrograms/ml of mafosfamide, as compared to control. These results strongly suggest that high concentrations of mafosfamide may be useful for the purging of autologous BMC from CML cells.
AuthorsM Nieborowska-Skórska, T Skórski, M Z Ratajczak, C Szczylik, L Malaguarnera, B Calabretta
JournalFolia histochemica et cytobiologica (Folia Histochem Cytobiol) Vol. 31 Issue 4 Pg. 161-7 ( 1993) ISSN: 0239-8508 [Print] Poland
PMID8137996 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Oligonucleotide Probes
  • mafosfamide
  • Cyclophosphamide
  • perfosfamide
Topics
  • Antineoplastic Agents (therapeutic use)
  • Blast Crisis (pathology, therapy)
  • Bone Marrow (drug effects, pathology)
  • Bone Marrow Purging
  • Colony-Forming Units Assay
  • Cyclophosphamide (analogs & derivatives, pharmacology, therapeutic use)
  • Drug Screening Assays, Antitumor
  • Humans
  • Leukemia, Myeloid, Chronic-Phase (pathology, therapy)
  • Oligonucleotide Probes
  • Polymerase Chain Reaction
  • Tumor Cells, Cultured

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