High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia

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Abstract

The recurrent t(12;21)(p12;q22) translocation fuses two genes, TEL and AML1, that have previously been shown to be independently involved in myeloid malignant proliferations. A search for rearrangement of the TEL locus in the region known to be involved in t(12;21) was performed by Southern blotting in a panel of hematopoietic malignancies. The presence of a t(12;21) was confirmed by fluorescence in situ hybridization (FISH) and/or reverse transcriptase (RT)-polymerase chain reaction (PCR). We report that fusion of TEL to AML1 is specifically observed in at least 16% of the childhood B- lineage acute lymphoblastic leukemia (ALL) investigated, none of which had been previously identified as harboring t(12;21).

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Romana, S. P., Poirel, H., Leconiat, M., Flexor, M. A., Mauchauffé, M., Jonveaux, P., … Bernard, O. A. (1995). High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood, 86(11), 4263–4269. https://doi.org/10.1182/blood.v86.11.4263.bloodjournal86114263

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