| Literature DB >> 31534006 |
Qian Zhang1, Hong Y Wang2, Xiaobin Liu2, Selene Nunez-Cruz2, Mowafaq Jillab3, Olga Melnikov3, Kavindra Nath4, Jerry Glickson4, Mariusz A Wasik1,3,5.
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.Entities:
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Year: 2019 PMID: 31534006 DOI: 10.4049/jimmunol.1801327
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422