作者
Anna M Eiring, Jason G Harb, Paolo Neviani, Christopher Garton, Joshua J Oaks, Riccardo Spizzo, Shujun Liu, Sebastian Schwind, Ramasamy Santhanam, Christopher J Hickey, Heiko Becker, Jason C Chandler, Raul Andino, Jorge Cortes, Peter Hokland, Claudia S Huettner, Ravi Bhatia, Denis C Roy, Stephen A Liebhaber, Michael A Caligiuri, Guido Marcucci, Ramiro Garzon, Carlo M Croce, George A Calin, Danilo Perrotti
发表日期
2010/3/5
期刊
Cell
卷号
140
期号
5
页码范围
652-665
出版商
Elsevier
简介
MicroRNAs and heterogeneous ribonucleoproteins (hnRNPs) are posttranscriptional gene regulators that bind mRNA in a sequence-specific manner. Here, we report that loss of miR-328 occurs in blast crisis chronic myelogenous leukemia (CML-BC) in a BCR/ABL dose- and kinase-dependent manner through the MAPK-hnRNP E2 pathway. Restoration of miR-328 expression rescues differentiation and impairs survival of leukemic blasts by simultaneously interacting with the translational regulator poly(rC)-binding protein hnRNP E2 and with the mRNA encoding the survival factor PIM1, respectively. The interaction with hnRNP E2 is independent of the microRNA's seed sequence and it leads to release of CEBPA mRNA from hnRNP E2-mediated translational inhibition. Altogether, these data reveal the dual ability of a microRNA to control cell fate both through base pairing with mRNA targets and through a decoy …
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