» Articles » PMID: 23926303

A Role for IRF4 in the Development of CLL

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2013 Aug 9
PMID 23926303
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Interferon regulatory factor 4 (IRF4) is a critical transcriptional regulator of B-cell development and function. A recent genome-wide single-nucleotide polymorphism (SNP) association study identified IRF4 as a major susceptibility gene in chronic lymphocytic leukemia (CLL). Although the SNPs located in the IRF4 gene were linked to a downregulation of IRF4 in CLL patients, whether a low level of IRF4 is critical for CLL development remains unclear. In rodents, CLL cells are derived from B1 cells whose population is dramatically expanded in immunoglobulin heavy chain Vh11 knock-in mice. We bred a Vh11 knock-in allele into IRF4-deficient mice (IRF4(-/-)Vh11). Here, we report that IRF4(-/-)Vh11 mice develop spontaneous early-onset CLL with 100% penetrance. Further analysis shows that IRF4(-/-)Vh11 CLL cells proliferate predominantly in spleen and express high levels of Mcl-1. IRF4(-/-)Vh11 CLL cells are resistant to apoptosis but reconstitution of IRF4 expression in the IRF4(-/-)Vh11 CLL cells inhibits their survival. Thus, our study demonstrates for the first time a causal relationship between low levels of IRF4 and the development of CLL. Moreover, our findings establish IRF4(-/-)Vh11 mice as a novel mouse model of CLL that not only is valuable for dissecting molecular pathogenesis of CLL but could also be used for therapeutic purposes.

Citing Articles

Research and analysis of differential gene expression in CD34 hematopoietic stem cells in myelodysplastic syndromes.

Wang M, Liao C, Wei X, Xie Y, Han P, Yu Y PLoS One. 2025; 20(3):e0315408.

PMID: 40073065 PMC: 11902259. DOI: 10.1371/journal.pone.0315408.


The dynamic functions of IRF4 in B cell malignancies.

Maffei R, Fiorcari S, Atene C, Martinelli S, Mesini N, Pilato F Clin Exp Med. 2022; 23(4):1171-1180.

PMID: 36495369 PMC: 10390622. DOI: 10.1007/s10238-022-00968-0.


Reduced IRF4 expression promotes lytic phenotype in Type 2 EBV-infected B cells.

Bristol J, Brand J, Ohashi M, Eichelberg M, Casco A, Nelson S PLoS Pathog. 2022; 18(4):e1010453.

PMID: 35472072 PMC: 9041801. DOI: 10.1371/journal.ppat.1010453.


Notch2 Increases the Resistance to Venetoclax-Induced Apoptosis in Chronic Lymphocytic Leukemia B Cells by Inducing Mcl-1.

Fiorcari S, Maffei R, Atene C, Mesini N, Maccaferri M, Leonardi G Front Oncol. 2022; 11:777587.

PMID: 35070982 PMC: 8770925. DOI: 10.3389/fonc.2021.777587.


Molecular interactions of IRF4 in B cell development and malignancies.

Sundararaj S, Casarotto M Biophys Rev. 2022; 13(6):1219-1227.

PMID: 35059038 PMC: 8724474. DOI: 10.1007/s12551-021-00825-6.


References
1.
Hardy R, Wei C, Hayakawa K . Selection during development of VH11+ B cells: a model for natural autoantibody-producing CD5+ B cells. Immunol Rev. 2004; 197:60-74. DOI: 10.1111/j.0105-2896.2004.0100.x. View

2.
Laine J, Kunstle G, Obata T, Sha M, Noguchi M . The protooncogene TCL1 is an Akt kinase coactivator. Mol Cell. 2000; 6(2):395-407. DOI: 10.1016/s1097-2765(00)00039-3. View

3.
Chen S, Batliwalla F, Holodick N, Yan X, Yancopoulos S, Croce C . Autoantigen can promote progression to a more aggressive TCL1 leukemia by selecting variants with enhanced B-cell receptor signaling. Proc Natl Acad Sci U S A. 2013; 110(16):E1500-7. PMC: 3631671. DOI: 10.1073/pnas.1300616110. View

4.
Allan J, Sunter N, Bailey J, Pettitt A, Harris R, Pepper C . Variant IRF4/MUM1 associates with CD38 status and treatment-free survival in chronic lymphocytic leukaemia. Leukemia. 2010; 24(4):877-81. DOI: 10.1038/leu.2009.298. View

5.
Longo P, Laurenti L, Gobessi S, Sica S, Leone G, Efremov D . The Akt/Mcl-1 pathway plays a prominent role in mediating antiapoptotic signals downstream of the B-cell receptor in chronic lymphocytic leukemia B cells. Blood. 2007; 111(2):846-55. DOI: 10.1182/blood-2007-05-089037. View