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Protection of Bone Marrow Stromal Cells from the Toxic Effects of Cyclophosphamide in Vivo and of ASTA-Z 7557 and Etoposide in Vitro by Ammonium Trichloro(dioxyethylene-O-O')tellurate (AS101)¹

Cancer AIDS and Immunology Research Institute, Department of Life Sciences, Bar Ilan University, Ramat Gan 52900, Israel

The immunomodulator AS101 has previously been shown to protect mice from lethal and sublethal doses of cyclophosphamide (CYP), AS101 was also shown to protect BM granulocyte-macrophage colony-forming cells from the toxic effects of ASTA-Z 7557. In the present study we examined the ability of AS101 to protect functional properties of BM stromal cells from the toxic effects of CYP in vivo or ASTA-Z in vitro. The functional properties of stromal cells from CYP-injected mice were tested with respect to stromal cell number and viability as reflected by the number of colony-forming unit fibroblasts, the ability of established stromal layers to secrete colony-stimulating factor and interleukin 6, as well as the capacity to support hemopoletic cells. All of these parameters were tested from day 1 to day 7 after CYP treatment. We demonstrate that all stromal functions are severely damaged following CYP treatment. Pretreatment of mice with 10 µg AS101 24 h before injection of 250 mg/kg CYP resulted in a significant amelioration of stromal cell functions as early as 24 h following CYP treatment. In addition we show that prior incubation of BM cells with AS101 protects the development of stromal colony-forming unit fibroblasts from the toxic effects of ASTA-Z, a potent derivative of CYP, and etoposide, a derivative of podophyllotoxin. These results strongly suggest the usefulness of AS101 in counteracting chemotherapy-induced BM microenvironmental suppression and the important role of the compound as an adjunct treatment of cancer when used in combination with CYP. The data also suggest that effectiveness of AS101 in purging bone marrow when used concomitantly with ASTA-Z or etoposide.

¹ Partly supported by the Israeli Cancer Research Fund and the Dave and Florence Muskovitz Chair in Cancer Research. This work comprises part of a doctoral study in the Department of Life Sciences, Bar Ilan University.

² To whom requests for reprints should be addressed, at C.A.I.R. Institute, Department of Life Sciences, Bar Ilan University, Ramat Gan 52900, Israel.

Received 7/10/92. Accepted 2/ 8/93.

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