Abstract
Reciprocal t(16;21)(p11;q22) is a rare chromosomal abnormality in acute myeloid leukemia (AML). The chimeric transcript FUS-ERG formed by this translocation which causes the replacement of RNA-binding domain of FUS (alias TLS) with the DNA-binding domain of ERG, and this event is thought to be responsible for leukemogenesis. Here we report two cases of AML with t(16;21)(p11.2;q22) showing unusual characteristics, and address the clinical, hematological, and molecular aspects of leukemia with t(16;21), along with a review of the literature.
Original language | English |
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Pages (from-to) | 111-118 |
Number of pages | 8 |
Journal | Cancer genetics and cytogenetics |
Volume | 194 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2009 Oct 15 |
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Genetics
- Cancer Research