A unique platform that accurately recapitulates leukemia phenotypes in vivo, the AML Patient-Derived Xenograft (PDX) models are designed to promote the optimal leukemia conditions.
Model Number | Diagnosis | Mutational Profile | NSG™-SGM3 Engraftment | Ara-C Responsive |
---|---|---|---|---|
J000106132* | Acute Myelocytic Leukemia | FLT3+, NPM1+, DNMT3A+, and IDH1+ | 20% AML at 8 weeks | Yes |
J000106134* | Acute Myelocytic Leukemia, M4 | FLT3+ and NPM1+ | 45% AML at 8 weeks | Yes |
J000106566* | Acute Myelocytic Leukemia | TP53+ | 35% AML at 8 weeks | Yes |
J000106124* | Acute Myelocytic Leukemia, secondary | No mutations identified | 80% AML at 8 weeks | Not Characterized |
J000106143* | Acute Myelocytic Leukemia | TP53+ and CUX1+ | 20% AML at 8 weeks | Not Characterized |
J000106565* | Acute Myelocytic Leukemia M4/M5 | FLT3 ITD+, FLT3 TKD+, and NPM1+ | 15% AML at 8 weeks | Not Characterized |
J000106569* | Acute Myelocytic Leukemia | FLT3-ITD+ and NPM1+ | 10% AML at 8 weeks | Not Characterized |
*Passaged Models
*Passaged Model
Percent Engraftment of AML J000106132
PDX J000106132 averages 20% engraftment at 8 weeks and 70% at 12 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
Ara-C Response in AML Model J000106132
J000106132 AML NSG-SGM3™ mice. Growth rate of AML samples detected in peripheral blood in the presence or absence of Ara-C. Mice were engrafted with human AML cells (hCD33+) and treated +/- Ara-C (30mg/kg) for five consecutive days.
*Passaged Model
Percent Engraftment of AML J000106134
PDX J000106134 averages 45% engraftment at 8 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
ARA-C RESPONSE IN AML MODEL J000106134
J000106134 AML NSG™-SGM3 mice. Growth rate of AML samples detected in peripheral blood in the presence or absence of Ara-C. Mice were engrafted with human AML cells (hCD33+) and treated +/- Ara-C (30mg/kg) for five consecutive days.
*Passaged Model
Percent Engraftment of AML J000106566
PDX J000106566 averages 10% engraftment at 6 weeks and 35% at 8 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
ARA-C RESPONSE IN AML MODEL J000106566
J000106566 AML NSG™-SGM3 mice. Growth rate of AML samples detected in peripheral blood in the presence or absence of Ara-C. Mice were engrafted with human AML cells (hCD33+) and treated +/- Ara-C (30mg/kg) for five consecutive days.
*Passaged Model
Percent Engraftment of AML J000106124
PDX J000106124 averages averages 80% engraftment at 8 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
*Passaged Model
Percent Engraftment of AML J000106143
PDX J000106143 averages 50% engraftment at 12 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
*Passaged Model
Percent Engraftment of AML J000106565
PDX J000106565 averages 15% engraftment at 8 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
*Passaged Model
Percent Engraftment of AML J000106569
PDX J000106569 averages 10% engraftment at 8 weeks and 57% at 12 weeks post engraftment in peripheral blood of NSG™-SGM3 mice.
The currently available models are confirmed to engraft in the NSG™-SGM3 mice.
Greater than 5% AML in the peripheral blood of NSG™-SGM3 mice 10-16 weeks post engraftment.
A minimum of 15 mice is required. Approximately 100-500 mice in total can be engrafted depending on the model of interest.
Some AML tumor models in our portfolio were passaged in vivo. This approach allows JAX to continuously supply the models and retain inventory for use in further studies at later dates if needed.
The average time to confirm AML engraftment in the peripheral blood of NSG™-SGM3 mice is 8 weeks post injection.
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