Abstract
Inhibitors of Bruton tyrosine kinase (BTK), a kinase downstream of BCR, display remarkable activity in a subset of mantle cell lymphoma (MCL) patients, but the drug resistance remains a considerable challenge. In this study, we demonstrate that aberrant expression of ROR1 (receptor tyrosine kinase-like orphan receptor 1), seen in a large subset of MCL, results in BCR/BTK–independent signaling and growth of MCL cells. ROR1 forms a functional complex with CD19 to persistently activate the key cell signaling pathways PI3K–AKT and MEK–ERK in the BCR/BTK–independent manner. This study demonstrates that ROR1/CD19 complex effectively substitutes for BCR–BTK signaling to promote activation and growth of MCL cells. Therefore, ROR1 expression and activation may represent a novel mechanism of resistance to inhibition of BCR/BTK signaling in MCL. Our results provide a rationale to screen MCL patients for ROR1 expression and to consider new therapies targeting ROR1 and/or CD19 or their downstream signaling pathways for MCL-expressing ROR1.
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CITATION STYLE
Zhang, Q., Wang, H. Y., Liu, X., Nunez-Cruz, S., Jillab, M., Melnikov, O., … Wasik, M. A. (2019). Cutting Edge: ROR1/CD19 Receptor Complex Promotes Growth of Mantle Cell Lymphoma Cells Independently of the B Cell Receptor–BTK Signaling Pathway. The Journal of Immunology, 203(8), 2043–2048. https://doi.org/10.4049/jimmunol.1801327
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