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t(5;21)(q13;q22)

Clinics and Pathology

Disease myelodysplastic syndrome (MDS) and acute non lymphocytic leukemia (ANLL)
Phenotype / cell stem origin 1 case of refractory anemia with excess of blastsin transformation (RAEB-t), 1 MDS evolving towards a M4-ANLL, 2 M2-ANLL, and 1 ANLL not otherwise specified
Epidemiology 5 cases to date; 3M/2F, aged 58 yr (median, range: 31-75)

Cytogenetics

Cytogenetics Morphological sole anomaly in 2 cases, complex karyotypes in 2 other cases.

Genes involved and Proteins

Note The gene in 5q13 is yet unknown, and, because cryptic t(12;21) ETV6 /AML1 are not rare, it is therefore uncertain whether this translocation involve a new AML1 partner
Gene Name AML1
Location 21q22
Dna / Rna transcription is from telomere to centromere
Protein contains a Runt domain and, in the C-term, a transactivation domain; forms heterodimers; widely expressed; nuclear localisation; transcription factor (activator) for various hematopoietic-specific genes

External links

Other databaset(5;21)(q13;q22) Mitelman database (CGAP - NCBI)
Other databaset(5;21)(q13;q22) CancerChromosomes (NCBI)

To be noted

Additional cases are needed to delineate the epidemiology of this rare entity:
you are welcome to submit a paper to our new Case Report section.

Bibliography

Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia.
Mitelman F, Nilsson PG, Brandt L, Alimena G, Gastaldi R, Dallapiccola B
Cancer genetics and cytogenetics. 1981 ; 4 (3) : 197-214.
PMID 7317873
 
A new translocation, t(5;21)(q13;q22) in acute myelogenous leukemia.
Gogineni SK, da Costa M, Verma RS
Cancer genetics and cytogenetics. 1996 ; 88 (2) : 167-169.
PMID 8640729
 
CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: association with prior therapy.
Roulston D, Espinosa R 3rd, Nucifora G, Larson RA, Le Beau MM, Rowley JD
Blood. 1998 ; 92 (8) : 2879-2885.
PMID 9763573
 
Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
Kakazu N, Taniwaki M, Horiike S, Nishida K, Tatekawa T, Nagai M, Takahashi T, Akaogi T, Inazawa J, Ohki M, Abe T
Genes, chromosomes & cancer. 1999 ; 26 (4) : 336-345.
PMID 10534769
 
Concurrent translocations of MLL and CBFA2 (AML1) genes with new partner breakpoints in a child with secondary myelodysplastic syndrome after treatment of acute lymphoblastic leukemia.
Mathew S, Head D, Rubnitz JE, Raimondi SC
Genes, chromosomes & cancer. 2000 ; 28 (2) : 227-232.
PMID 10825008
 
Testicular infiltration in acute myeloid leukemia with complex karyotype including t(8;21).
Giagounidis AA, Hildebrandt B, Braunstein S, Aivado M, Germing U, Heinsch M, Aul C
Annals of hematology. 2002 ; 81 (2) : 115-118.
PMID 11907795
 

Contributor(s)

Written02-2003Jean-Loup Huret

Citation

This paper should be referenced as such :
Huret JL . t(5;21)(q13;q22). Atlas Genet Cytogenet Oncol Haematol. February 2003 .
URL : http://AtlasGeneticsOncology.org/Genes/t0521q13q22ID1174.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Jul 14 16:33:08 2008


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