Maier Julia, Lechel André, Marienfeld Ralf, Barth Thomas F E, Möller Peter, Mellert Kevin
Institute of Pathology, University Hospital Ulm, 89081 Ulm, Germany.
Department of Internal Medicine I, University of Ulm, 89081 Ulm, Germany.
Cancers (Basel). 2022 Jan 21;14(3):531. doi: 10.3390/cancers14030531.
Richter syndrome (RS) is defined as the transformation of chronic lymphocytic leukemia (CLL) into an aggressive lymphoma, mostly diffuse large B-cell lymphoma (DLBCL). Despite intensive therapy, patients with RS have an unfavorable clinical outcome. The detailed pathobiology of Richter transformation still needs to be elucidated. Here, we report high mRNA and protein levels of in the RS cell line U-RT1. Co-immunoprecipitation revealed the assembly of a CBM complex using CARD9 instead of CARD11. CARD9 is known to be an activator of NF-кB signaling in myeloid cells. U-RT1 Western blot analyses showed phosphorylation of IκB as well as IKK, indicating a constitutively active canonical NF-кB pathway. This was further supported by the significant reduction in cell viability and CYLD cleavage products after CARD9 siRNA knockdown. We also showed immunostaining for CARD9 in 53% of cases analyzed in a series of RS tissue specimens, whereas other lymphomas rarely show expression. This is the first report on ectopic expression and function of CARD9 in an aggressive B-cell lymphoma. Our findings suggest that CARD9 may contribute to the pathogenesis of RS.
里氏综合征(RS)被定义为慢性淋巴细胞白血病(CLL)转化为侵袭性淋巴瘤,主要是弥漫性大B细胞淋巴瘤(DLBCL)。尽管进行了强化治疗,RS患者的临床结局仍不理想。里氏转化的详细病理生物学仍有待阐明。在此,我们报告了RS细胞系U-RT1中 的高mRNA和蛋白质水平。免疫共沉淀显示使用CARD9而非CARD11组装了CBM复合物。已知CARD9是髓系细胞中NF-κB信号通路的激活剂。U-RT1蛋白质免疫印迹分析显示IκB以及IKK的磷酸化,表明经典NF-κB途径持续激活。CARD9小干扰RNA敲低后细胞活力和CYLD裂解产物显著减少进一步支持了这一点。我们还在一系列RS组织标本分析的53%病例中显示了CARD9的免疫染色,而其他淋巴瘤很少显示 表达。这是关于CARD9在侵袭性B细胞淋巴瘤中异位表达和功能的首次报道。我们的发现表明CARD9可能参与了RS的发病机制。