t(8;11)(p11;p15) NUP98/WHSC1L1
2005-03-01 Jean-Loup Huret   Affiliation1.Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
Clinics and Pathology
Disease
Acute myeloid leukemia (AML)
Note
Possibly heterogenous (see data on genes).
Epidemiology
3 cases to date: 1 M1-AML, 1 M4-AML and 1 case not otherwise specified; two male patients were aged 50 and 64 years.
Prognosis
One patient died during induction therapy, another one achieved complete remission and was alive at 19 months+.
Genes Involved and Proteins
Note
Gene name
NSD3 (nuclear receptor binding SET domain protein 3)
Location
8p11.23
Protein description
Suggested role in chromatin remodeling.
Gene name
NUP98 (nucleoporin 98 kDa)
Location
11p15.4
Protein description
Nuclear membrane localisation; nucleoporin: associated with the nuclear pore complex; role in nucleocytoplasmic transport processes.
Result of the Chromosomal Anomaly
Transcript
A 5 NUP98 - 3 NSD3 fusion transcript was detected; the reciprocal transcript was also expressed. The breakpoints occurred between exons 11 and 12 of NUP98 and betweeen exons 3 and 4 in WHSC1L1/NSD3.
Article Bibliography
| Pubmed ID | Last Year | Title | Authors |
|---|---|---|---|
| 6627222 | 1983 | The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: a 12-year study (1970-1982). | Larson RA et al |
| 11986249 | 2002 | NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15). | Rosati R et al |
| 11550283 | 2001 | Identification of four new translocations involving FGFR1 in myeloid disorders. | Sohal J et al |
Summary
Fusion gene
NUP98/WHSC1L1 NUP98 (11p15.4) WHSC1L1 (8p11.23) M t(8;11)(p12;p15)|NUP98/WHSC1L1 NUP98 (11p15.4) WHSC1L1 (8p11.23) TIC
Citation
Jean-Loup Huret
t(8;11)(p11;p15) NUP98/WHSC1L1
Atlas Genet Cytogenet Oncol Haematol. 2005-03-01
Online version: http://atlasgeneticsoncology.org/haematological/1200/t(8
