Molecular Pathways: Targeting MALT1 Paracaspase Activity in Lymphoma

被引:27
作者
Fontan, Lorena [1 ,2 ]
Melnick, Ari [1 ,2 ]
机构
[1] Weill Cornell Med Coll, Dept Med, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Pharmacol, New York, NY 10065 USA
关键词
NF-KAPPA-B; T-CELL; IN-VITRO; PROTEASE ACTIVITY; BCL6; ACTIVATION; MECHANISMS; INHIBITOR; CLEAVAGE; PATHOGENESIS;
D O I
10.1158/1078-0432.CCR-12-3869
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MALT1 mediates the activation of NF-kappa B in response to antigen receptor signaling. MALT1, in association with BCL10 and CARD11, functions as a scaffolding protein to activate the inhibitor of I kappa B kinase (IKK) complex. In addition, MALT1 is a paracaspase that targets key proteins in a feedback loop mediating termination of the NF-kappa B response, thus promoting activation of NF-kB signaling. Activated B-cell subtype of diffuse large B-cell lymphomas (ABC-DLBCL), which tend to be more resistant to chemotherapy, are often biologically dependent on MALT1 activity. Newly developed MALT1 small-molecule inhibitors suppress the growth of ABC-DLBCLs in vitro and in vivo. This review highlights the recent advances in the normal and disease-related functions of MALT1. Furthermore, recent progress targeting MALT1 proteolytic activity raises the possibility of deploying MALT1 inhibitors for the treatment of B-cell lymphomas and perhaps autoimmune diseases that involve increased B-or T-cell receptor signaling. (C) 2013 AACR.
引用
收藏
页码:6662 / 6668
页数:7
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