Journal
INTERNATIONAL JOURNAL OF CANCER
Volume 123, Issue 9, Pages 2222-2227Publisher
WILEY
DOI: 10.1002/ijc.23772
Keywords
preclinical models; acute leukemia; circulating endothelial progenitors
Categories
Funding
- sixth EU Framework Programme [504743]
- AIRC (Associazione Italiana per la Ricerca sul Cancro)
- ISS (Istituto Superiore di Sanita)
- NIH [CA34196]
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Transplantation of human acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) primary cells and cell lines in different strains of immunodeficient mice has led to preclinical models extensively used to investigate acute leukemia stem cells, biology and drug sensitivity. We studied the engraftment kinetics of AML and ALL id cell likes and primary cells in 3 strains of NOD.CB17-Prkdc(scid) (NOD/scid, NS)-related mice (NOD.Cg-Prkdc(scid)B2m(tm1Unc)/J, abbreviated NOD/scid/beta 2 null, NSB; and NOD. Cg-Prkdc(scid)Il2 rg(tm1Wjll)/SzJ, abbreviated NOD/scid/IL-2R gamma null, NSG). The engraftment of human malignant cells was investigated by means of clinicopathological criteria, How cytometry, PCR and immunobistochemistrv. In NSG mice, we observed a significantly faster development of leukemia-related symptoms and a higher percentage of leukemia cells in the blood, in the marrow and in the spleen. The leukemia-related angiogenic switch (measured as the number of circulating endothelial cells and progenitors) was faster in NSG compared to NS and NSB mice. These models will be instrumental to studies on leukemia-initiating stein cells, leukemia biology, preclinical treatment studies, and to obtain patient-specific preclinical models to design and investigate patient-tailored therapies. (C) 2008 Wiley-Liss, Inc.
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