Kang Heejae, Maurer Lisa M, Cheng Jing, Smyers Mei, Klei Linda R, Hu Dong, Hofstatter Azambuja Juliana, Murai Marcelo J, Mady Ahmed, Ahmad Ejaz, Trotta Matthew, Klei Hanna B, Liu Minda, Ekambaram Prasanna, Nikolovska-Coleska Zaneta, Chen Bill B, McAllister-Lucas Linda M, Lucas Peter C
Department of Pathology and.
Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Clin Invest. 2025 Apr 15;135(8). doi: 10.1172/JCI164573.
Diffuse large B cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma, and the activated B cell-like subtype (ABC-DLBCL) is associated with particularly poor outcome. Many ABC-DLBCLs harbor gain-of-function mutations that cause inappropriate assembly of the CARMA1-BCL10-MALT1 (CBM) signalosome, a cytoplasmic complex that drives downstream NF-κB signaling. MALT1 is the effector protein of the CBM signalosome such that its recruitment to the signalosome via interaction with BCL10 allows it to exert both protease and scaffolding activities that together synergize in driving NF-κB. Here, we demonstrate that a molecular groove located between two adjacent immunoglobulin-like domains within MALT1 represents a binding pocket for BCL10. Leveraging this discovery, we performed an in silico screen to identify small molecules that dock within this MALT1 groove and act as BCL10-MALT1 protein-protein interaction (PPI) inhibitors. We report the identification of M1i-124 as a first-in-class compound that blocks BCL10-MALT1 interaction, abrogates MALT1 scaffolding and protease activities, promotes degradation of BCL10 and MALT1 proteins, and specifically targets ABC-DLBCLs characterized by dysregulated MALT1. Our findings demonstrate that small-molecule inhibitors of BCL10-MALT1 interaction can function as potent agents to block MALT1 signaling in selected lymphomas, and provide a road map for clinical development of a new class of precision-medicine therapeutics.
弥漫性大B细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤类型,其中活化B细胞样亚型(ABC-DLBCL)的预后尤其差。许多ABC-DLBCL存在功能获得性突变,这些突变导致CARMA1-BCL10-MALT1(CBM)信号小体组装异常,CBM信号小体是一种驱动下游NF-κB信号传导的细胞质复合物。MALT1是CBM信号小体的效应蛋白,通过与BCL10相互作用被招募到信号小体,使其能够发挥蛋白酶和支架活性,共同协同驱动NF-κB。在此,我们证明MALT1中两个相邻免疫球蛋白样结构域之间的分子凹槽代表BCL10的结合口袋。利用这一发现,我们进行了计算机筛选,以鉴定能够对接在该MALT1凹槽内并作为BCL10-MALT1蛋白-蛋白相互作用(PPI)抑制剂的小分子。我们报告鉴定出M1i-124,这是一种一流的化合物,可阻断BCL10-MALT1相互作用,消除MALT1的支架和蛋白酶活性,促进BCL10和MALT1蛋白的降解,并特异性靶向以MALT1失调为特征的ABC-DLBCL。我们的研究结果表明,BCL10-MALT1相互作用的小分子抑制剂可作为强效药物,阻断特定淋巴瘤中的MALT1信号传导,并为一类新型精准医学疗法的临床开发提供了路线图。