Literature DB >> 3896474

Comparative in vitro effects of cyclophosphamide derivatives on murine bone marrow-derived stromal and hemopoietic progenitor cell classes.

J P de Jong, P G Nikkels, K G Brockbank, R E Ploemacher, J S Voerman.   

Abstract

We investigated the in vitro effects of ASTA-Z-7595, ASTA-Z-7557, ASTA-Z-7654, and 4-hydroperoxycyclophosphamide (4HC) on murine stromal fibroblastoid colony-forming units, committed hemopoietic progenitors (erythroid burst-forming units and granulocyte/macrophage colony-forming units), and pluripotent hemopoietic stem cells assayed by the spleen colony-forming unit (CFU-s) assay. In general, the drugs showed a time-and dose-dependent effect on colony-forming unit survival, and the relative toxicities were in the order in which the drugs are listed above. We found a relative sparing of day 12 CFU-s compared with day 7 CFU-s and committed hemopoietic and stromal progenitors, although colony size of day 12 CFU-s was reduced. Our results support two possible mechanisms for delayed or inadequate hemopoietic reconstitution in clinical studies using bone marrow purged with 4-hydroperoxycyclophosphamide or ASTA-Z-7557, i.e., damage to (a) transplantable stromal cells or (b) the hemopoietic stem cells.

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Year:  1985        PMID: 3896474

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  3 in total

Review 1.  Bone marrow purging with mafosfamide--a critical survey.

Authors:  H Sindermann; M Peukert; P Hilgard
Journal:  Blut       Date:  1989-11

2.  A cellular analysis of long-term haematopoietic damage in mice after repeated treatment with cyclophosphamide.

Authors:  G Molineux; C Xu; J Hendry; N G Testa
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

3.  Cumulative bone marrow stromal damage caused by X-irradiation and cytosine-arabinoside in leukemic mice.

Authors:  Z Ben-Ishay; G Prindull; S Yankelev; S Sharon
Journal:  Med Oncol Tumor Pharmacother       Date:  1990
  3 in total

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