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Both NUP98/TOP1 and TOP1/NUP98 transcripts are detected in a de novo AML with t(11;20)(p15;q11)

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GENES CHROMOSOMES & CANCER
卷 38, 期 1, 页码 102-105

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WILEY
DOI: 10.1002/gcc.10239

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The NUP98 gene is involved in several chromosomal abnormalities associated with acute leukemia. The recurrent t(11; 20)(p15;q11) chromosomal translocation results in generation of the NUP981TOP1 chimeric gene. This abnormality has been observed primarily in therapy-related leukemias, and TOP1/NUP98 transcripts have not been demonstrated. We describe a case of de novo acute myeloid leukemia with t(11;20)(p15;q11), with no known history of exposure to chemicals. The translocation occurred in intron 13 of NUP98 and intron 7 of TOP1, as in the three previously reported cases. The breakpoint in NUP98 was exactly the same as that found in a previously reported case. In addition, a reciprocal TOP1/NUP98 transcript was detected for the first time in our patient. (C) 2003 Wiley-Liss, Inc.

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