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
Published online Feb 6, 2016. doi: 10.5315/wjh.v5.i1.1
(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 |
Gene(s) studied | Chromosomal location | Frequency in human MDS | Equivalent human MDS subtype according to WHO 2008 classification | Ref. |
Transcription factors | ||||
NUP98-HOXD13 | t(2;11)(q31;p15) | Rare | RCMD | [69] |
RUNX1 | 21q22.3 | 15%-40% | RAEB | [105] |
EVI1 | 3q26.2 | Rare | RCMD | [136] |
SALL4 | 20q13.2 | 15%-40% | RCMD | [139] |
NPM1 | 5q35.1 | About 4% | RCMD | [138] |
Signalling molecules | ||||
NRAS | 1p13.2 | About 20% | RAEB | [142] |
BCL2 | 18q21.33 | Unknown | ||
PTEN | 10q23.3 | Unknown | RCMD | [140] |
SHIP | 2q37.1 | Unknown | ||
Epigenetic regulators | ||||
TET2 | 4q24 | 20%-30% | RCMD/CMML | [115] |
ASXL1 | 20q11.21 | 15%-20% | RCMD | [122,123] |
EZH2 | 7q36.1 | 2%-6% | RCMD/MPN | [141] |
MLL5 | 7q22.1 | Unknown | No definitive MDS | [145] |
RNA spliceosome | ||||
SRSF2 | 17q25.2 | 15%-30% | RCMD | [98] |
U2AF1 | 21q22.3 | 11% | No definitive MDS | [100] |
SF3B1 | 2q33.1 | 10%-20% | RARS, RARS-T | [101] |
Telomere function | ||||
TERT | 5p15.33 | Unknown | RCMD | [124] |
5q- | ||||
RPS14 | 5q33.1 | About 10% | 5q-like | [91] |
CD74-SMIM3 (NID67) | 5q32-q33.1 | [92] | ||
SPARC | 5q33.1 | [97] | ||
MIR145/146A | 5q32-34 | [143] | ||
APC | 5q22.2 | [99] | ||
CSNK1A1 | 5q32 | [94] |
Gene(s) studied | Model/technique | Tractability to human MDS | Ref. | |||||||
Anemia | Multi-lineage cytopenias | Dysplasia | Bone marrow cellularity | HSPC skewing | Secondary leukemia | Latency to leukemia | Survival | |||
NUP98-HOXD13 | Transgenic | Yes | Yes | Yes | Hyper- | Yes | Yes2 | 14 mo | - | [69] |
Cd74-Nid67 | Large scale chromosomal deletion, RPS14 haploinsufficient | Yes | No | Yes | Hypo- | Yes | No | - | 1 | [92] |
SPARC | Knock-out | No | No | Yes | 1 | 1 | No | - | 1 | [97] |
MIR-145, MIR146a | Retroviral transduction | No | No | Yes | 1 | 1 | Yes | 4-14 mo | - | [143] |
APC | Transgenic, haploinsufficient | Yes | No | Yes | 1 | Yes | No | - | 3-8 mo | [99] |
Csnk1a1 | Transgenic, inducible | Yes | Yes | Yes | Yes | Yes | No | - | 1 | [94] |
Srsf2 | Transgenic, inducible | Yes | Yes | Yes | Normal | Yes | No | - | 1 | [98] |
U2af1 | Transgenic, inducible | No | No | No | Normal | Yes | No | - | - | [100] |
Sf3b1 | Transgenic, haploinsufficient | Yes | No | Yes | 1 | 1 | No | - | About 12 mo | [101] |
RUNX1-D171N | Retroviral transduction | Yes | Yes | Yes | Normal to hyper- | 1 | Yes | 4-13 mo | - | [105] |
RUNX1-S291fsX300 | Retroviral transduction | Yes | Yes | Yes | Normal to hyper- | 1 | Yes | 4-13 mo | - | [105] |
RUNX1S291fs/Ezh2 | Retroviral transduction | Yes | Yes | Yes | Variable | 1 | No | - | 262 d | [125] |
Tet2 | Transgenic, hypomorphic | Yes | Yes | Yes | Hyper- | Yes | No | - | 11 mo | [115] |
Tet2/Ezh2 | Transgenic, inducible | Yes | Yes | Yes | Hyper- | Yes | No | - | 10 mo | [141] |
ASXL1 | Transgenic, inducible | Yes | Yes | Yes | Hypo- | Yes | No | - | Median 50 wk | [122] |
Asxl1 | Transgenic, constitutive | Yes | Yes | Yes | Normal to hyper- | Yes3 | 16 mo | 8-42 d | - | [123] |
TERT | Transgenic, inducible | Yes | Yes | Yes | Hyper | Yes | Yes | 1 | 12 mo | [124] |
Evi1 | Retroviral transduction | Yes | Yes | Yes | Hyper- | 1 | No | - | 10-12 mo | [136] |
SALL4 | Transgenic | Yes | Yes | Yes | Hyper- | Yes | Yes | 6 wk to 12 mo | - | [139] |
Npm1 | Transgenic, haploinsufficient | No | No | Yes | Hyper | No | Yes | 24 mo | - | [138] |
NRASD12-BCL2 | Transgenic, inducible/constitutive | 1 | No | Yes | 1 | Yes | Yes | 3-6 mo | - | [142] |
Pten/Ship | Transgenic, Pten +/- Ship -/- | Yes | Yes | 1 | Hypo | Yes | No | - | 5 wk | [140] |
Dido | Knock-out | Yes | No | Yes | 1 | 1 | No | - | 1 | [137] |
Arid4a | Knock-out | Yes | Yes | Yes | Hyper- | 1 | Yes | 5 mo | - | [144] |
Mll5 | Knock-out | Yes | No | No | 1 | 1 | No | - | - | [145] |
- Citation: Tan SY, Smeets MF, Chalk AM, Nandurkar H, Walkley CR, Purton LE, Wall M. Insights into myelodysplastic syndromes from current preclinical models. World J Hematol 2016; 5(1): 1-22
- URL: https://www.wjgnet.com/2218-6204/full/v5/i1/1.htm
- DOI: https://dx.doi.org/10.5315/wjh.v5.i1.1