田邊 賢司
Department Research Institutes and Facilities, Research Institutes and Facilities Position Associate Professor |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukaemia. |
Journal | Formal name:British journal of haematology |
Volume, Issue, Page | 135,pp.336-347 |
Author and coauthor | Ichikawa, Hitoshi Tanabe, Kenji Mizushima, Hiroshi Hayashi, Yasuhide Mizutani, Shuki Ishii, Eiichi Hongo, Teruaki Kikuchi, Akira Satake, Masanobu |
Authorship | 2nd author |
Publication date | 2006 |
Summary | Human acute myeloid leukaemia (AML) involving a core-binding factor (CBF) transcription factor is called CBF leukaemia. In these leukaemias, AML1 (RUNX1, PEBP2alphaB, CBFalpha2)-MTG8 (ETO) and CBFbeta (PEBP2beta)-MYH11 chimaeric proteins are generated by t(8;21) and inv(16) respectively. We analysed gene expression profiles of leukaemic cells by microarray, and selected genes whose expression appeared to be modulated in association with t(8;21) and inv(16). In a pair-wise comparison, 15% of t(8;21)-associated transcripts exhibited high or low expression in inv(16)-AML, and 26% of inv(16)-associated transcripts did so equivalently in t(8;21)-AML. These common elements in gene expression profiles between t(8;21)- and inv(16)-AML probably reflect the situation that AML1-MTG8 and CBFbeta-MYH11 chimaeric proteins affect a common set of target genes in CBF leukaemic cells. On the other hand, 38% of t(8;21)-associated and 24% of inv(16)-associated transcripts were regulated in t(8;21)- and inv(16)-specific manners. These distinct features of t(8;21)- and inv(16)-associated genes correlate with the bimodular structures of the chimaeric proteins (CBF-related AML1 and CBFbeta portions, and CBF-unrelated MTG8 and MYH11 portions). |