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. 2019 Jan 21;20(2):453. doi: 10.3390/ijms20020453

Table 3.

AML mouse models based on viral transduction and transplantation.

Year Transgene Viral Vector Cellular Target Phenotype Ref.
1990 BCR-ABL pMSCV-pgk-neo Total BM Myeloproliferative malignancy, ALL and CML-like [111]
1997 MLL-ENL pMSCV-IRES-GFP Thy-1loSca-1+Hi-2Khi, 5-FU treated BM Self-renewal in vitro & AML in vivo [117]
2002 RUNX1-ETO pMSCV-IRES-GFP HSC c-Kit + Sca-1 Lin Myeloid developmental abnormality but no AML [118]
2003 MLL-GAS7 pMSCV-pgk-neo HSPC Mixed lineage leukaemia phenotype [120]
2004 MOZ-TIF2, BCR-ABL pMSCV-IRES-GFP CMP, GMP MOZ-TIF2 but not BCR-ABL resulted in transplantable AML in vivo [114]
2006 MLL-AF9 pMSCV-IRES-GFP GMP Transplantation of transduced cells propagated in MC resulted in AML in vivo [115]
2011 MN1 pMSCV-pgk-neo CMP, GMP CMP are susceptible for MN1 transformation, GMP required co-expression of MEIS1 for AML induction [121]
2012 MLL-AF9 pMSCV-pgk-puro Evi1+/− MLL-AF9 transduced cells Knockdown of Evi1 delayed leukaemia induction in vivo [116]

FU (Fluorouracil), MC (methylcellulose).