Cutting edge: ROR1/CD19 receptor complex promotes growth of mantle cell lymphoma cells independently of the b cell receptor-BTK signaling pathway

Qian Zhang, Hong Y. Wang, Xiaobin Liu, Selene Nunez-Cruz, Mowafaq Jillab, Olga Melnikov, Kavindra Nath, Jerry Glickson, Mariusz A. Wasik

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

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.

Original languageEnglish
Pages (from-to)2043-2048
Number of pages6
JournalJournal of Immunology
Volume203
Issue number8
DOIs
StatePublished - Oct 15 2019

Keywords

  • Adenine/analogs & derivatives
  • Agammaglobulinaemia Tyrosine Kinase/antagonists & inhibitors
  • Cell Line, Tumor
  • Cell Proliferation/drug effects
  • Dose-Response Relationship, Drug
  • Humans
  • Lymphoma, Mantle-Cell/drug therapy
  • Piperidines
  • Protein Kinase Inhibitors/pharmacology
  • Pyrazoles/pharmacology
  • Pyrimidines/pharmacology
  • Receptor Tyrosine Kinase-like Orphan Receptors/antagonists & inhibitors
  • Receptors, Antigen, B-Cell/antagonists & inhibitors
  • Receptors, Antigen, T-Cell/antagonists & inhibitors
  • Signal Transduction/drug effects
  • Structure-Activity Relationship

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