Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/36854
Title: A role for eukaryotic initiation factor 4B overexpression in the pathogenesis of diffuse large B-cell lymphoma
Authors: Horvilleur, E.
Sbarrato, T.
Hill, K.
Spriggs, R. V.
Screen, M.
Goodrem, P. J.
Sawicka, K.
Chaplin, L. C.
Touriol, C.
Packham, G.
Potter, K. N.
Dirnhofer, S.
Tzankov, A.
Dyer, Martin J. S.
Bushell, M.
MacFarlane, M.
Willis, A. E.
First Published: 1-Nov-2013
Publisher: Nature Publishing Group
Citation: Leukemia, 2014, 28 (5), pp. 1092-1102
Abstract: Dysregulated expression of factors that control protein synthesis is associated with poor prognosis of many cancers, but the underlying mechanisms are not well defined. Analysis of the diffuse large B-cell lymphoma (DLBCL) translatome revealed selective upregulation of mRNAs encoding anti-apoptotic and DNA repair proteins. We show that enhanced synthesis of these proteins in DLBCL is mediated by the relief of repression that is normally imposed by structure in the 5'-untranslated regions of their corresponding mRNAs. This process is driven by signaling through mammalian target of rapamycin, resulting in increased synthesis of eukaryotic initiation factor (eIF) 4B complex (eIF4B), a known activator of the RNA helicase eIF4A. Reducing eIF4B expression alone is sufficient to decrease synthesis of proteins associated with enhanced tumor cell survival, namely DAXX, BCL2 and ERCC5. Importantly, eIF4B-driven expression of these key survival proteins is directly correlated with patient outcome, and eIF4B, DAXX and ERCC5 are identified as novel prognostic markers for poor survival in DLBCL. Our work provides new insights into the mechanisms by which the cancer-promoting translational machinery drives lymphomagenesis.
DOI Link: 10.1038/leu.2013.295
ISSN: 0887-6924
eISSN: 1476-5551
Links: http://www.nature.com/leu/journal/v28/n5/full/leu2013295a.html
http://hdl.handle.net/2381/36854
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © 2014 Macmillan Publishers Limited. This work is licensed under a Creative Commons Attribution- NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
Appears in Collections:Published Articles, Dept. of Cancer Studies and Molecular Medicine

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