ETV6/AML1 fusion by FISH in adult acute lymphoblastic leukemia
- 1 April 2002
- journal article
- Published by Springer Nature in Leukemia
- Vol. 16 (4), 669-674
- https://doi.org/10.1038/sj.leu.2402435
Abstract
Dual-color interphase fluorescence in situ hybridization (FISH) with ETV6 and AML1 probes was used for the first time on a series of 159 adult patients with acute lymphoblastic leukemia (ALL), for detection of the t(12;21)(p13;q22) translocation. Seven patients (4.4%) were found, with 50-100% of positive cells, of whom one of two tested, proved negative for the fusion product by RT-PCR. Two of them, aged 43 and 50 years, are the oldest patients so far confirmed to have the translocation. Three who relapsed at 10, 11 and 24 months, suggest that adults may not enjoy the good short-term prognosis reported for t(12;21)-positive children. Thirty-one-negative cases had signal numbers differing from the two expected for each gene. In 15 cases these results were consistent with the karyotype. In nine cases with uninformative cytogenetics, the numbers were consistent with those for centromeres and indicated a hidden aneuploidy. Loss of ETV6 genes in two cases and AML1 amplification in three others were not suspected from the cytogenetics. In conclusion, FISH proved to be reliable in defining ETV6/AML1 positivity in this group of patients as well as providing valuable insights into negative cases.Keywords
This publication has 22 references indexed in Scilit:
- The genetics of childhood acute lymphoblastic leukaemiaBest Practice & Research Clinical Haematology, 2000
- CorrespondenceLeukemia Research, 2000
- Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in SpainBritish Journal of Haematology, 1999
- High rate of chromosome abnormalities detected by fluorescence in situ hybridization using BCR and ABL probes in adult acute lymphoblastic leukemiaLeukemia, 1998
- TEL‐AML1 fusion in acute lymphoblastic leukaemia of adultsBritish Journal of Haematology, 1996
- Tandem triplication and quadruplication of chromosome 21 in childhood acute lymphoblastic leukemiaCancer Genetics and Cytogenetics, 1996
- Probes for hidden hyperdiploidy in acute lymphoblastic leukaemiaGenes, Chromosomes and Cancer, 1996
- Partial chromosome 21 amplification in a child with acute lymphoblastic leukemiaGenes, Chromosomes and Cancer, 1995
- t( 12;21): A new recurrent translocation in acute lymphoblastic leukemiaGenes, Chromosomes and Cancer, 1994
- Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemiaBlood, 1986