| Literature DB >> 12874791 |
Satsuki Iwase1, Nobutake Akiyama, Tetsuaki Sekikawa, Shinobu Saito, Yasuhiro Arakawa, Junko Horiguchi-Yamada, Hisashi Yamada.
Abstract
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 NUP98/TOP1 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. Copyright 2003 Wiley-Liss, Inc.Entities:
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Year: 2003 PMID: 12874791 DOI: 10.1002/gcc.10239
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006