Classification
AML with recurrent cytogenetic anomalies
AML with multilineage dysplasia
therapy-related AML and myelodysplastic syndrome
AML not otherwise categorised
Molecular biology
Four genes had been found to be fused to a variety of partner genes in AML:
AML1 (RUNX1) (MIM.151385)
MLL (MIM.159555)
MOZ (MIM.601408)
TEL (ETV6) (MIM.600618)
NUP98 (MIM.601021) - NUP98/HOXD11 by t(2;11)(q31;p15) (MIM.142986) - NUP98/HOXD13 (MIM.142989)
Translocations involving 11q23 are acute monoblastic leukemia (AML-M5) and acute myelomonocytic leukemia (AMML-M4)
MLL/GMPS
MLL/FBP17
MLL/LPP
MLL/GPH
MLL/PNUTL1
MLL/CDK6
MLL/LASP1
MLL/GRAF
MLL/ABI1
MLL/AF9 fusion gene from translocation t(9;11)(p22;q23)
References
Nerlov C. C/EBPalpha mutations in acute myeloid leukaemias. Nat Rev Cancer. 2004 May;4(5):394-400. PMID: #15122210#
Tenen DG. Disruption of differentiation in human cancer: AML shows the way. Nat Rev Cancer. 2003 Feb;3(2):89-101. PMID: #12563308#
Vardiman JW, Harris NL, Brunning RD. The World Health Organization (WHO) classification of the myeloid neoplasms. Blood. 2002 Oct 1;100(7):2292-302. PMID: #12239137#