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Preleukemia in long-term plasmacytoma-regressor mice

O Sagi-Assif1, L Trakhtenbrot, D Douer

  • 1Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel.

International Journal of Cancer
|June 4, 1998
PubMed
Summary

Chemotherapy survivors may harbor preleukemic cells. Adoptive transfer of these cells from plasmacytoma-regressor mice (PRM) induced leukemia in recipients, suggesting a model for chemotherapy-related leukemia.

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Area of Science:

  • Immunology
  • Hematology
  • Oncology

Background:

  • Melphalan chemotherapy for plasmacytoma can cause persistent immunohematological abnormalities in mice.
  • These abnormalities include immunosuppression, myeloproliferation, and altered growth factor responses.
  • Mice without plasmacytoma treated with melphalan do not develop these issues.

Purpose of the Study:

  • To investigate the potential for preleukemic cells in mice that survived plasmacytoma chemotherapy.
  • To determine if these preleukemic cells can induce leukemia in recipient mice.

Main Methods:

  • Adoptive transfer of splenocytes from plasmacytoma-regressor mice (PRM) to irradiated syngeneic recipients.
  • Monitoring recipients for leukemia development via blood counts and spleen histology.

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  • Secondary adoptive transfer of cells from primary recipients to non-irradiated secondary recipients.
  • Sex chromosome analysis to confirm cell origin.
  • Characterization of leukemic cells for surface markers.
  • Main Results:

    • Plasmacytoma-regressor mice harbor preleukemic cells that do not progress to leukemia in the host.
    • Adoptive transfer of splenocytes from PRM induced overt leukemia in irradiated recipients.
    • Leukemia developed in 100% of secondary recipients after transfer from primary recipients.
    • Sex chromosome analysis confirmed leukemic cells originated from PRM donors.
    • Established leukemic lines expressed hematopoietic progenitor and T cell markers.

    Conclusions:

    • Plasmacytoma-regressor mice contain transplantable preleukemic cells.
    • These cells can induce leukemia in recipient mice, indicating a potential mechanism for chemotherapy-related leukemia.
    • PRM serve as a valuable animal model for studying the development of chemotherapy-induced leukemia.