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IRF4 Mediates the Oncogenic Effects of STAT3 in Anaplastic Large Cell Lymphomas

Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino 10126, Italy
Center for Experimental Research and Medical Studies (CeRMS), University of Torino, Torino 10126, Italy
Department of Oncology and Hemato-Oncology, University of Milan, Milan 20122, Italy
Department of Experimental and Health Sciences, University Pompeu Fabra, Barcelona 08003, Spain
Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara 28100, Italy
Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065, USA
Candiolo Cancer Institute, FPO-IRCCS, Candiolo 10060, Italy
Lymphoma and Genomics Research Program, IOR Institute of Oncology Research, Bellinzona 6500, Switzerland
Center for Translational Genomics and Bioinformatics, San Raffaele Scientific Institute, Milan 20132, Italy
Neuroscience Institute Cavalieri Ottolenghi, University of Turin, Turin 10043, Italy
Molecular Biotechnology Center, University of Torino, Torino 10126, Italy
Department of Oncology, University of Torino, Candiolo 10060, Italy
Author to whom correspondence should be addressed.
These authors contributed equally to this study.
Cancers 2018, 10(1), 21;
Received: 27 November 2017 / Revised: 9 January 2018 / Accepted: 12 January 2018 / Published: 18 January 2018
(This article belongs to the Special Issue Targeting ALK in Cancer)
Systemic anaplastic large cell lymphomas (ALCL) are a category of T-cell non-Hodgkin’s lymphomas which can be divided into anaplastic lymphoma kinase (ALK) positive and ALK negative subgroups, based on ALK gene rearrangements. Among several pathways aberrantly activated in ALCL, the constitutive activation of signal transducer and activator of transcription 3 (STAT3) is shared by all ALK positive ALCL and has been detected in a subgroup of ALK negative ALCL. To discover essential mediators of STAT3 oncogenic activity that may represent feasible targets for ALCL therapies, we combined gene expression profiling analysis and RNA interference functional approaches. A shRNA screening of STAT3-modulated genes identified interferon regulatory factor 4 (IRF4) as a key driver of ALCL cell survival. Accordingly, ectopic IRF4 expression partially rescued STAT3 knock-down effects. Treatment with immunomodulatory drugs (IMiDs) induced IRF4 down regulation and resulted in cell death, a phenotype rescued by IRF4 overexpression. However, the majority of ALCL cell lines were poorly responsive to IMiDs treatment. Combination with JQ1, a bromodomain and extra-terminal (BET) family antagonist known to inhibit MYC and IRF4, increased sensitivity to IMiDs. Overall, these results show that IRF4 is involved in STAT3-oncogenic signaling and its inhibition provides alternative avenues for the design of novel/combination therapies of ALCL. View Full-Text
Keywords: anaplastic large cell lymphomas; ALK; STAT3; IRF4; immunomodulatory drugs; JQ1 anaplastic large cell lymphomas; ALK; STAT3; IRF4; immunomodulatory drugs; JQ1
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MDPI and ACS Style

Bandini, C.; Pupuleku, A.; Spaccarotella, E.; Pellegrino, E.; Wang, R.; Vitale, N.; Duval, C.; Cantarella, D.; Rinaldi, A.; Provero, P.; Di Cunto, F.; Medico, E.; Bertoni, F.; Inghirami, G.; Piva, R. IRF4 Mediates the Oncogenic Effects of STAT3 in Anaplastic Large Cell Lymphomas. Cancers 2018, 10, 21.

AMA Style

Bandini C, Pupuleku A, Spaccarotella E, Pellegrino E, Wang R, Vitale N, Duval C, Cantarella D, Rinaldi A, Provero P, Di Cunto F, Medico E, Bertoni F, Inghirami G, Piva R. IRF4 Mediates the Oncogenic Effects of STAT3 in Anaplastic Large Cell Lymphomas. Cancers. 2018; 10(1):21.

Chicago/Turabian Style

Bandini, Cecilia, Aldi Pupuleku, Elisa Spaccarotella, Elisa Pellegrino, Rui Wang, Nicoletta Vitale, Carlotta Duval, Daniela Cantarella, Andrea Rinaldi, Paolo Provero, Ferdinando Di Cunto, Enzo Medico, Francesco Bertoni, Giorgio Inghirami, and Roberto Piva. 2018. "IRF4 Mediates the Oncogenic Effects of STAT3 in Anaplastic Large Cell Lymphomas" Cancers 10, no. 1: 21.

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