Review
Copyright ©The Author(s) 2016.
World J Hematol. Feb 6, 2016; 5(1): 1-22
Published online Feb 6, 2016. doi: 10.5315/wjh.v5.i1.1
Table 1 Bethesda diagnostic criteria for myeloid dysplasia in mice
(1) At least one of the following
A: Neutropenia
B: Thrombocytopenia (without leucocytosis or erythrocytosis)
C: Anemia (without leucocytosis or thrombocytosis)
(2) Maturation defect in myeloid cells manifest as at least one of
A: Dysgranulopoiesis, dyserythropoiesis, or dysplastic megakaryocytes with or without increased myeloid immature forms or blasts
B: At least 20% myeloid immature forms or blasts
(3) Disorder is not AML
Subclassification
Myelodysplastic syndrome if meeting criteria (2)A
Cytopenia with increased blasts if meeting (2)B
Table 2 Candidate genes used to model myelodysplastic syndromes in mice and their correlation to human myelodysplastic syndromes
Gene(s) studiedChromosomal locationFrequency in human MDSEquivalent human MDS subtype according to WHO 2008 classificationRef.
Transcription factors
NUP98-HOXD13t(2;11)(q31;p15)RareRCMD[69]
RUNX121q22.315%-40%RAEB[105]
EVI13q26.2RareRCMD[136]
SALL420q13.215%-40%RCMD[139]
NPM15q35.1About 4%RCMD[138]
Signalling molecules
NRAS1p13.2About 20%RAEB[142]
BCL218q21.33Unknown
PTEN10q23.3UnknownRCMD[140]
SHIP2q37.1Unknown
Epigenetic regulators
TET24q2420%-30%RCMD/CMML[115]
ASXL120q11.2115%-20%RCMD[122,123]
EZH27q36.12%-6%RCMD/MPN[141]
MLL57q22.1UnknownNo definitive MDS[145]
RNA spliceosome
SRSF217q25.215%-30%RCMD[98]
U2AF121q22.311%No definitive MDS[100]
SF3B12q33.110%-20%RARS, RARS-T[101]
Telomere function
TERT5p15.33UnknownRCMD[124]
5q-
RPS145q33.1About 10%5q-like[91]
CD74-SMIM3 (NID67)5q32-q33.1[92]
SPARC5q33.1[97]
MIR145/146A5q32-34[143]
APC5q22.2[99]
CSNK1A15q32[94]
Table 3 Published mouse models of myelodysplastic syndromes
Gene(s) studiedModel/techniqueTractability to human MDS
Ref.
AnemiaMulti-lineage cytopeniasDysplasiaBone marrow cellularityHSPC skewingSecondary leukemiaLatency to leukemiaSurvival
NUP98-HOXD13TransgenicYesYesYesHyper-YesYes214 mo-[69]
Cd74-Nid67Large scale chromosomal deletion, RPS14 haploinsufficientYesNoYesHypo-YesNo-1[92]
SPARCKnock-outNoNoYes11No-1[97]
MIR-145, MIR146aRetroviral transductionNoNoYes11Yes4-14 mo-[143]
APCTransgenic, haploinsufficientYesNoYes1YesNo-3-8 mo[99]
Csnk1a1Transgenic, inducibleYesYesYesYesYesNo-1[94]
Srsf2Transgenic, inducibleYesYesYesNormalYesNo-1[98]
U2af1Transgenic, inducibleNoNoNoNormalYesNo--[100]
Sf3b1Transgenic, haploinsufficientYesNoYes11No-About 12 mo[101]
RUNX1-D171NRetroviral transductionYesYesYesNormal to hyper-1Yes4-13 mo-[105]
RUNX1-S291fsX300Retroviral transductionYesYesYesNormal to hyper-1Yes4-13 mo-[105]
RUNX1S291fs/Ezh2Retroviral transductionYesYesYesVariable1No-262 d[125]
Tet2Transgenic, hypomorphicYesYesYesHyper-YesNo-11 mo[115]
Tet2/Ezh2Transgenic, inducibleYesYesYesHyper-YesNo-10 mo[141]
ASXL1Transgenic, inducibleYesYesYesHypo-YesNo-Median 50 wk[122]
Asxl1Transgenic, constitutiveYesYesYesNormal to hyper-Yes316 mo8-42 d-[123]
TERTTransgenic, inducibleYesYesYesHyperYesYes112 mo[124]
Evi1Retroviral transductionYesYesYesHyper-1No-10-12 mo[136]
SALL4TransgenicYesYesYesHyper-YesYes6 wk to 12 mo-[139]
Npm1Transgenic, haploinsufficientNoNoYesHyperNoYes24 mo-[138]
NRASD12-BCL2Transgenic, inducible/constitutive1NoYes1YesYes3-6 mo-[142]
Pten/ShipTransgenic, Pten +/- Ship -/-YesYes1HypoYesNo-5 wk[140]
DidoKnock-outYesNoYes11No-1[137]
Arid4aKnock-outYesYesYesHyper-1Yes5 mo-[144]
Mll5Knock-outYesNoNo11No--[145]