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NUP98 Rearrangement in Acute Myelomonocytic Leukemia With t(11;19)(p15;p12): The First Case Report Worldwide

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초록

Dear Editor, AML is a group of heterogeneous diseases derived from various cytogenetic and molecular abnormalities that are significant for diagnosis, treatment, and prognosis in many cases. We report a rare case of AML harboring t(11;19)(p15;p12) that was detected with whole-genome sequencing (WGS).

Abstract

Dear Editor, AML is a group of heterogeneous diseases derived from various cytogenetic and molecular abnormalities that are significant for diagnosis, treatment, and prognosis in many cases. We report a rare case of AML harboring t(11;19)(p15;p12) that was detected with whole-genome sequencing (WGS).

참고문헌 (6)

  1. Singer S, "Nuclear pore component Nup98 is a potential tumor suppressor and regulates posttranscriptional expression of select p53 target genes", Mol Cell, 48, pp.799~810 (2012)
  2. Cronshaw JM, "Proteomic analysis of the mammalian nuclear pore complex", J Cell Biol, 158, pp.915~927 (2002)
  3. Gu BW, "Major form of NUP98", HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity, 2003, pp.17, 1858~1864
  4. Borrow J, "The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9", Nat Genet, 12, pp.159~167 (1996)
  5. Nakamura T, "Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia", Nat Genet, 12, pp.154~158 (1996)
  6. Gough SM, "NUP98 gene fusions and hematopoietic malignancies: common themes and new biologic insights", Blood, 118, pp.6247~6257 (2011)

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