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E-GEOD-22434 - Expression data from Evi1-transduced primary bone marrow cells

Status
Released on 8 July 2010, last updated on 14 September 2015
Organism
Mus musculus
Samples (8)
Array (1)
Protocols (8)
Description
Evi1 is essential for proliferation of hematopoietic stem cells and implicated in the development of myeloid disorders. Particularly, high Evi1 expression defines one of the largest clusters in acute myeloid leukemia and is significantly associated with extremely poor prognosis. Improvement of the therapeutic outcome of leukemia with activated Evi1 is one of the most challenging issues. However, mechanistic basis of Evi1-mediated leukemogenesis has not been fully elucidated. Here we show that Evi1 directly represses PTEN transcription in the murine bone marrow, which leads to activation of AKT/mTOR signaling. In a murine bone marrow transplantation model, Evi1 leukemia showed remarkable sensitivity to an mTOR inihibitor rapamycin. Furthermore, we found that Evi1 binds to several polycomb group proteins and recruits polycomb repressive complexes for PTEN downregulation, which reveals a novel epigenetic mechanism of AKT/mTOR activation in leukemia. Expression analyses and chromatin immunoprecipitation assays using human samples indicate that our findings in mice models are recapitulated in human leukemic cells. Dependence of Evi1-expressing leukemic cells on AKT/mTOR signaling provides the first example of targeted therapeutic modalities that suppress the leukemogenic activity of Evi1. The PTEN/AKT/mTOR signaling pathway and the Evi1-polycomb interaction can be promising therapeutic targets for leukemia with activated Evi1. Gene expression analysis for the purpose of identifying the target genes of Evi1 in primary bone marrow. 5-FU-primed mononuclear bone marrow cells harvested from C57/B6 mice were retrovirally transduced with Evi1-GFP or GFP. GFP positive cells were sorted and analyzed by Affymetrix® Mouse Genome 430 2.0 Array® for gene expression. Four independent experiments were performed.
Experiment type
transcription profiling by array 
Contacts
Akihide Yoshimi <ayoshimi-tky@umin.ac.jp>, Yasuhito Nannya <ynanya-tky@umin.ac.jp>, Eriko Nitta, Masahiro Nakagawa, Mineo Kurokawa, Munetake Shimabe, Naoko Watanabe-Okochi, Shunya Arai, Susumu Goyama, Tomohiko Sato, Toshio Kitamura, Yoichi Imai, Yumiko Yoshiki
Citation
Evi1 represses PTEN expression and activates PI3K/AKT/mTOR via interactions with polycomb proteins. Yoshimi A, Goyama S, Watanabe-Okochi N, Yoshiki Y, Nannya Y, Nitta E, Arai S, Sato T, Shimabe M, Nakagawa M, Imai Y, Kitamura T, Kurokawa M.
MIAME
PlatformsProtocolsVariablesProcessedRaw
Files
Investigation descriptionE-GEOD-22434.idf.txt
Sample and data relationshipE-GEOD-22434.sdrf.txt
Raw data (1)E-GEOD-22434.raw.1.zip
Processed data (1)E-GEOD-22434.processed.1.zip
Array designA-AFFY-45.adf.txt
Links