Cooperative signaling through the signal transducer and activator of transcription 3 and nuclear factor-kappa B pathways in subtypes of diffuse large B-cell lymphoma

作者：Lam Lloyd T; Wright George; Davis R Eric; Lenz Georg; Farinha Pedro; Dang Lenny; Chan John W; Rosenwald Andreas; Gascoyne Randy D; Staudt Louis M^*

来源：Blood, 2008, 111(7): 3701-3713.

DOI：10.1182/blood-2007-09-111948

The activated B cell-like (ABC) subgroup of diffuse large B-cell lymphoma (DLBCL) is characterized by constitutive activation of the nuclear factor-kappa B (NF-kappa B) pathway. In this study, we showed that the NF-kappa B pathway induced the expression of the cytokines interleukin (IL)-6 and IL-1 0 in ABC DLBCL cell lines, which also have high levels of total and phosphorylated signal transducer and activator of transcription (STAT) 3 protein, suggesting autocrine signaling. Using RNA interference for STAT3, we defined a gene expression signature of IL-6 and IL-10 signaling through STAT3. Based on this signature, we constructed a molecular predictor of STAT3 signaling that defined a subset of ABC DLBCL tumors with high expression of STAT3, IL-6, and/or IL-10 and their downstream targets. Although the STAT3-high and STAT3-low subsets had equivalent expression of genes that distinguish ABC DLBCL from germinal center B cell-like DLBCL, STAT3-high ABC DLBCLs had higher expression of signatures that reflected NF-kappa B activity, proliferation, and glycolysis. A small-molecule inhibitor of Janus kinase signaling, which blocked STAT3 signature expression, was toxic only for ABC DLBCL lines and synergized with an inhibitor of NF-kappa B signaling. These findings suggest that the biological interplay between the STAT3 and NF-kappa B pathways may be exploited for the treatments of a subset of ABC DLBCLs.

• 出版日期2008-4-1