View source for HAEM4:Acute Myeloid Leukemia (AML) with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2);GATA2, MECOM

{{DISPLAYTITLE:Acute Myeloid Leukemia (AML) with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2);GATA2, MECOM}}


<blockquote class='blockedit'>{{Box-round|title=PREVIOUS EDITION|This page from the 4th edition of Haematolymphoid Tumours is being updated. See 5th edition [[HAEM5:Table_of_Contents|Table of Contents]].
}}</blockquote>
==Primary Author(s)*==

Gordana Raca MD PhD, University of Southern California, Los Angeles

__TOC__

[[File:inv(3)(q21q26.2).png|inv(3)(q21q26.2)]]
[[File:t(3;3)(q21;q26.2).png|t(3;3)(q21;q26.2)]]

==Cancer Category/Type==

Acute Myeloid Leukemia (AML)

==Cancer Sub-Classification / Subtype==

Acute myeloid leukemia (AML) with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM

==Definition / Description of Disease==

The  inv(3)(q21q26.2)/t(3;3)(q21;q26.2) defines a distinctive cytogenetic subtype of acute myeloid leukemia (AML) in 2008 WHO classification (AML with inv(3)(q21q26.2)/t(3;3)(q21;q26.2), although it is currently not recognized as an abnormality pathognomonic for diagnosis of  AML irrespective of blast percentage. This abnormality also occurs in myelodysplastic syndrome (MDS), where it is associated with aggressive course and a high risk of progression to AML. It can also rarely be found in other myeloid neoplasms, including chronic myelogenous leukemia (mostly during accelerated phase or in blast crisis), other myeloproliferative neoplasms (MPN), and in overlap MDS/MPNs including chronic myelomonocytic leukemia<ref name=":0">{{Cite journal|last=Rogers|first=Heesun J.|last2=Vardiman|first2=James W.|last3=Anastasi|first3=John|last4=Raca|first4=Gordana|last5=Savage|first5=Natasha M.|last6=Cherry|first6=Athena M.|last7=Arber|first7=Daniel|last8=Moore|first8=Erika|last9=Morrissette|first9=Jennifer J. D.|date=2014|title=Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study|url=https://www.ncbi.nlm.nih.gov/pubmed/24463215|journal=Haematologica|volume=99|issue=5|pages=821–829|doi=10.3324/haematol.2013.096420|issn=1592-8721|pmc=4008101|pmid=24463215}}</ref>.

inv(3)(q21q26.2) and t(3;3)(q21;q26.2) are variant rearrangements with similar consequences at the molecular level and similar disease associations and clinical implications.  

In addition to the balanced inversion and translocation involving the bands 3q21 and 3q26.2, other 3q abnormalities are also common in AML.  A study of 6515 adults with newly diagnosed AML detected 3q abnormalities in 4.4% of the patients, and classified them in four categories<ref name=":1">{{Cite journal|last=Lugthart|first=Sanne|last2=Gröschel|first2=Stefan|last3=Beverloo|first3=H. Berna|last4=Kayser|first4=Sabine|last5=Valk|first5=Peter J. M.|last6=van Zelderen-Bhola|first6=Shama Lydia|last7=Jan Ossenkoppele|first7=Gert|last8=Vellenga|first8=Edo|last9=van den Berg-de Ruiter|first9=Eva|date=2010|title=Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia|url=https://www.ncbi.nlm.nih.gov/pubmed/20660833|journal=Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology|volume=28|issue=24|pages=3890–3898|doi=10.1200/JCO.2010.29.2771|issn=1527-7755|pmid=20660833}}</ref>:   

#t(3;3)/inv(3)
#Translocations involving only the band 3q26.2
#Translocations involving only the band 3q21
#Other 3q abnormalities.

Further studies are needed to determine how the molecular pathogenesis and clinical features of AML with other 3q rearrangements compare with the AML with inv(3)/t(3;3).

==Synonyms / Terminology==
AML with RPN1-MECOM

==Epidemiology / Prevalence==

AML with inv(3)(q21q26.2) and t(3;3)(q21;q26.2) comprises 1-2.5% of all AML cases and less than 1% of all MDS cases<ref name=":0" /><ref name=":1" />.

==Clinical Features==

The patients often present with anemia and normal or increased platelet counts. However, decreased platelet counts and hepatosplenomegaly can also be observed<ref name=":0" /><ref name=":1" />.

==Sites of Involvement==

Bone Marrow.

==Morphologic Features==

Common morphologic features include multilineage dysplasia, with atypical megakaryocytes (ie, small mono- or bilobed forms) and variable fibrosis.  The most consistent bone marrow finding in this disorder is an increase in the number of megakaryocytes, many of which are morphologically abnormal. In some patients, almost all of the identifiable megakaryocytes are micromegakaryocytes. 

==Immunophenotype==

Immunophenotypic studies typically show expression of CD13, CD33, HLA-DR, CD17(KIT) CD34 and CD38, occasionally with aberrant expression of CD7 and megakaryocytic markers like CD41 and CD61.

{| class="wikitable sortable"
|-
!Finding!!Marker
|-
|Positive (universal)||EXAMPLE CD1
|-
|Positive (subset)||EXAMPLE CD2
|-
|Negative (universal)||EXAMPLE CD3
|-
|Negative (subset)||EXAMPLE CD4
|}

==Chromosomal Rearrangements (Gene Fusions)==

Put your text here and/or fill in the table

{| class="wikitable sortable"
|-
!Chromosomal Rearrangement!!Genes in Fusion (5’ or 3’ Segments)!!Pathogenic Derivative!!Prevalence
|-
|EXAMPLE t(9;22)(q34;q11.2)||EXAMPLE 3'ABL1 / 5'BCR||EXAMPLE der(22)||EXAMPLE 5%
|-
|EXAMPLE t(8;21)(q22;q22)||EXAMPLE 5'RUNX1 / 3'RUNXT1||EXAMPLE der(8)||EXAMPLE 5%
|}		
			
==Characteristic Chromosomal Aberrations / Patterns==

Monosomy 7 is the most common associated (secondary) cytogenetic abnormality (in ~66% of cases), and appears to further contribute to the adverse prognosis of the inv(3q)/t(3;3) abnormality<ref name=":0" /><ref name=":1" />.
Complex karyotypes
Deletion 5q

==Genomic Gain/Loss/LOH==
Put your text here.

==Gene Mutations (SNV/INDEL)==

Secondary mutations are found in all AML cases with inv(3) ot t(3;3). Mutations in genes activating RAS/TK signaling pathway are the most common mutation.
  ''[[NRAS]]'' (~30%), ''[[ PTPN11]]''(11%), [[FLT3]] (13%) and ''[[KRAS]] (11%)'', as well as [[GATA2]] (15%) , ''[[RUNX1]]'' (12%) and ''[[NF1]]'' (9%) , [[CBL ]] (7%) , [[KIT]] (2%)<ref>{{Cite journal|last=Haferlach|first=C.|last2=Bacher|first2=U.|last3=Haferlach|first3=T.|last4=Dicker|first4=F.|last5=Alpermann|first5=T.|last6=Kern|first6=W.|last7=Schnittger|first7=S.|date=2011|title=The inv(3)(q21q26)/t(3;3)(q21;q26) is frequently accompanied by alterations of the RUNX1, KRAS and NRAS and NF1 genes and mediates adverse prognosis both in MDS and in AML: a study in 39 cases of MDS or AML|url=https://www.ncbi.nlm.nih.gov/pubmed/21283084|journal=Leukemia|volume=25|issue=5|pages=874–877|doi=10.1038/leu.2011.5|issn=1476-5551|pmid=21283084}}</ref>. [[CBL]] mutation is found often with concomitant GATA2 mutation.

===Other Mutations===
{| class="wikitable sortable"
|-
!Type!!Gene/Region/Other
|-
|Concomitant Mutations||[[GATA2]], [[CBL]]
|-
|Secondary Mutations||
|-
|Mutually Exclusive||
|}

==Epigenomics (Methylation)==

Put your text here

==Genes and Main Pathways Involved==

The ''[[MECOM]]'' (MDS1 and EVI1 complex locus)  gene in 3q26.3 is the key gene implicated in pathogenesis of AML with inv(3)/t(3;3). ''MECOM'' codes for several differentially spliced transcripts: MDS1-EVI1, MDS1 and EVI1. It consequently yields the MDS1-EVI1 [1239 amino acids (AA)], MDS1 (188AA) and EVI1 (1051AA) protein isoforms. While ''EVI1'' deregulated expression has been reported to be critical in stem cell self-renewal and leukaemogenesis, the roles of ''MDS1'' and MDS1-EVI1 in haematological malignancies remain unclear<ref name=":2">{{Cite journal|last=Wieser|first=Rotraud|date=2007|title=The oncogene and developmental regulator EVI1: expression, biochemical properties, and biological functions|url=https://www.ncbi.nlm.nih.gov/pubmed/17507183|journal=Gene|volume=396|issue=2|pages=346–357|doi=10.1016/j.gene.2007.04.012|issn=0378-1119|pmid=17507183}}</ref>. 

''[[EVI1]]'' is a zinc-finger nuclear transcription factor involved in many signaling pathways. It binds DNA through specific conserved sequences, interacts with   a number of transcriptional and epigenetic regulators (''[[CREBBP]]'', ''[[CTBP]]'', ''[[HDAC]]'', ''[[KAT2B]]'' (P/CAF), ''[[SMAD3]]'', ''[[GATA1]]'', ''[[GATA2]]'', ''[[DNMT3A]]'', and ''[[DNMT3B]]''), and mediates chromatin modifications and DNA hypermethylation. ''EVI1'' plays a role in embryogenesis and its deficiency in mice is an embryonic lethal mutation. Among the many other observed defects, ''EVI1''-/- mouse embryos have been shown to have defects in both the development and proliferation of hematopoietic stem cells (HSCs). It appears that depending on its binding partners, ''EVI1'' can act as a transcriptional activator to promote the proliferation of hematopoietic stem cells (eg, when bound to GATA2) or as a transcriptional repressor inhibiting erythroid differentiation (eg, when bound to GATA1)<ref name=":2" />.

[[File:Evi1.gata2.png|800px]]

Changes at mRNA level: ''EVI1'' proto-oncogene  has  early on been identified as aberrantly upregulated in almost all AML cases with inv(3) and t(3;3). Aberrant ''EVI1'' expression is also found in a majority of AML patients with other 3q26 abnormalities and even in patients with myeloid leukemia and a normal karyotype, suggesting that inappropriate activation of this gene occurs through various mechanisms<ref name=":3">{{Cite journal|last=Morishita|first=K.|last2=Parganas|first2=E.|last3=William|first3=C. L.|last4=Whittaker|first4=M. H.|last5=Drabkin|first5=H.|last6=Oval|first6=J.|last7=Taetle|first7=R.|last8=Valentine|first8=M. B.|last9=Ihle|first9=J. N.|date=1992|title=Activation of EVI1 gene expression in human acute myelogenous leukemias by translocations spanning 300-400 kilobases on chromosome band 3q26|url=https://www.ncbi.nlm.nih.gov/pubmed/1570317|journal=Proceedings of the National Academy of Sciences of the United States of America|volume=89|issue=9|pages=3937–3941|doi=10.1073/pnas.89.9.3937|issn=0027-8424|pmc=PMC525606|pmid=1570317}}</ref><ref>{{Cite journal|last=Russell|first=M.|last2=List|first2=A.|last3=Greenberg|first3=P.|last4=Woodward|first4=S.|last5=Glinsmann|first5=B.|last6=Parganas|first6=E.|last7=Ihle|first7=J.|last8=Taetle|first8=R.|date=1994|title=Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations|url=https://www.ncbi.nlm.nih.gov/pubmed/8049440|journal=Blood|volume=84|issue=4|pages=1243–1248|issn=0006-4971|pmid=8049440}}</ref><ref>{{Cite journal|last=Langabeer|first=S. E.|last2=Rogers|first2=J. R.|last3=Harrison|first3=G.|last4=Wheatley|first4=K.|last5=Walker|first5=H.|last6=Bain|first6=B. J.|last7=Burnett|first7=A. K.|last8=Goldstone|first8=A. H.|last9=Linch|first9=D. C.|date=2001|title=EVI1 expression in acute myeloid leukaemia|url=https://www.ncbi.nlm.nih.gov/pubmed/11167805|journal=British Journal of Haematology|volume=112|issue=1|pages=208–211|doi=10.1046/j.1365-2141.2001.02569.x|issn=0007-1048|pmid=11167805}}</ref>, but invariably confers an adverse prognosis. Interestingly, the breakpoints in chromosomal rearrangements that lead to ''EVI1'' activation in AML with inv(3)/t(3;3) were shown to occur  either 5' of the gene in the t(3;3) or 3' of the gene in the inv(3)<ref name=":3" />. It has long  been thought that activation of ''EVI1'' in malignant hematopoietic cells occurs by juxtaposition of the gene to enhancer elements of the housekeeping  ribophorin gene located at 3q21. However, several groups have recently described a novel molecular mechanism by which the inv(3)/t(3;3) re-positions a distal ''GATA2'' enhancer to activate ''MECOM'' expression, and simultaneously confer ''[[GATA2]]'' functional haploinsufficiency<ref>{{Cite journal|last=Gröschel|first=Stefan|last2=Sanders|first2=Mathijs A.|last3=Hoogenboezem|first3=Remco|last4=de Wit|first4=Elzo|last5=Bouwman|first5=Britta A. M.|last6=Erpelinck|first6=Claudia|last7=van der Velden|first7=Vincent H. J.|last8=Havermans|first8=Marije|last9=Avellino|first9=Roberto|date=2014|title=A single oncogenic enhancer rearrangement causes concomitant EVI1 and GATA2 deregulation in leukemia|url=https://www.ncbi.nlm.nih.gov/pubmed/24703711|journal=Cell|volume=157|issue=2|pages=369–381|doi=10.1016/j.cell.2014.02.019|issn=1097-4172|pmid=24703711}}</ref><ref>{{Cite journal|last=Yamazaki|first=Hiromi|last2=Suzuki|first2=Mikiko|last3=Otsuki|first3=Akihito|last4=Shimizu|first4=Ritsuko|last5=Bresnick|first5=Emery H.|last6=Engel|first6=James Douglas|last7=Yamamoto|first7=Masayuki|date=2014|title=A remote GATA2 hematopoietic enhancer drives leukemogenesis in inv(3)(q21;q26) by activating EVI1 expression|url=https://www.ncbi.nlm.nih.gov/pubmed/24703906|journal=Cancer Cell|volume=25|issue=4|pages=415–427|doi=10.1016/j.ccr.2014.02.008|issn=1878-3686|pmc=4012341|pmid=24703906}}</ref>.   This mechanism presents a new paradigm for the pathogenesis of MDS/AML. 

Changes at protein level: The inv(3)(q21q26.2)/t(3;3)(q21;q26.2) results in upregulation of the ''MECOM'' gene and increased levels of the EVI1 protein, but does not produce abnormal gene and protein fusions.

Key cellular pathways: ''EVI1'' has been shown to be involved in multiple downstream signaling pathways, including the transforming growth factor beta (TGF-β) signaling (where ''EVI1'' prevents transcription of the TGF-β induced anti-growth genes ) and ''[[JUN|c-Jun N-terminal kinase]]'' (JNK) signaling (where ''EVI1'' prevents phosphorylation  and activation of key transcription factors for the apoptotic response).

==Diagnostic Testing Methods==

#Karyotype: Inv(3) and t(3;3) can typically be detected by routine karyotype analysis, although the inversion may be challenging to identify in the cases with poor morphology.
#FISH: EVI1 break-apart FISH probe is commercially available and FISH testing is offered clinically by most clinical cytogenetic laboratories.

==Clinical Significance (Diagnosis, Prognosis and Therapeutic Implications)==

Diagnostic: The presence of inv(3)/t(3;3) defines a cytogenetic subtype of AML, however in the current WHO 2017 classification does not allow to make a diagnosis of AML if blast percentage <20%. Very poor prognosis and rapid progression of MDS with inv(3)(q21q26.2)/t(3;3)(q21;q26.2)  resulted in a proposal to consider neoplasms with these rearrangements as an AML  with recurrent genetic abnormalities, irrespective of blast percentage.

BCR-ABL1 positive patients with CML and concomitant MECOM rearrangement are considered in an aggressive phase of CML (Accelerated Phase) rather than de novo AML with inv(3)/t(3;3)

Prognostic: The inv(3)(q21q26.2)/t(3;3)(q21;q26.2)  is associated with a dismal prognosis in both AML and MDS. Review of  6515 adult patients with newly diagnosed AML enrolled in prospective European trials showed 5-year OS of only 5.7% +/- 3 for AML with inv(3)/t(3;3), with the median survival os 10.3 months. This adverse prognostic impact of inv(3)/t(3;3) appears to be further enhanced by additional monosomy 7 and/or complex karyotype. Similarly, the prognosis of MDS with inv(3)/t(3;3) is also poor, and the revised International Prognostic Scoring System (IPSS-R) for MDS includes inv(3)/t(3;3) among its poor risk cytogenetic abnormalities<ref name=":0" /><ref name=":1" />.

Therapeutic: AML with inv(3)(q21q26.2) or t(3;3) (q21;q26.2) is an aggressive disease with short survival, in need for novel and more efficient treatments. Some studies have shown that arsenic trioxide induces targeted specific degradation of the AML1/MDS1/EVI1 oncoprotein, and an isolated case report described  good response to Arsenic trioxide and thalidomide combination in a patient with MDS with inv(3)<ref>{{Cite journal|last=Shackelford|first=David|last2=Kenific|first2=Candia|last3=Blusztajn|first3=Agnieszka|last4=Waxman|first4=Samuel|last5=Ren|first5=Ruibao|date=2006|title=Targeted degradation of the AML1/MDS1/EVI1 oncoprotein by arsenic trioxide|url=https://www.ncbi.nlm.nih.gov/pubmed/17145882|journal=Cancer Research|volume=66|issue=23|pages=11360–11369|doi=10.1158/0008-5472.CAN-06-1774|issn=0008-5472|pmid=17145882}}</ref><ref>{{Cite journal|last=Raza|first=Azra|last2=Buonamici|first2=Silvia|last3=Lisak|first3=Laurie|last4=Tahir|first4=Sarah|last5=Li|first5=Donglan|last6=Imran|first6=Mehnaz|last7=Chaudary|first7=Nusrat Ijaz|last8=Pervaiz|first8=Hassan|last9=Gallegos|first9=J. Alejandro|date=2004|title=Arsenic trioxide and thalidomide combination produces multi-lineage hematological responses in myelodysplastic syndromes patients, particularly in those with high pre-therapy EVI1 expression|url=https://www.ncbi.nlm.nih.gov/pubmed/15203277|journal=Leukemia Research|volume=28|issue=8|pages=791–803|doi=10.1016/j.leukres.2003.11.018|issn=0145-2126|pmid=15203277}}</ref>.

==Familial Forms==

Put your text here

==Other Information==

Put your text here

==Links==

[[GATA2]]

[[MECOM]]

[http://www.uptodate.com/contents/cytogenetics-in-acute-myeloid-leukemia Up To Date Cytogenetics in AML]

[http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=3498 HNGC MECOM]

==References==
<references />

==Notes==
<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.













Edited by: Fabiola Quintero-Rivera 8/3/2018
[[Category:HAEM4]] [[Category:DISEASE]]