Figure 3.
Figure 3. BCR and MYD88 signaling pathways and potential targets. (A) Signaling through BCR leads to downstream activation of the NF-κB transcription factor, which is a driver pathway in ABC DLBCL. Signaling also activates the AKT/MTOR and MAP kinase pathways. Constitutive MYD88 signaling is an alternative pathway leading to NF-κB activation. (B) Inhibition of Btk by ibrutinib is toxic in ABC, but not in GCB DLBCL cell lines, providing evidence for the clinical relevance of the BCR signaling pathway.

BCR and MYD88 signaling pathways and potential targets. (A) Signaling through BCR leads to downstream activation of the NF-κB transcription factor, which is a driver pathway in ABC DLBCL. Signaling also activates the AKT/MTOR and MAP kinase pathways. Constitutive MYD88 signaling is an alternative pathway leading to NF-κB activation. (B) Inhibition of Btk by ibrutinib is toxic in ABC, but not in GCB DLBCL cell lines, providing evidence for the clinical relevance of the BCR signaling pathway.

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