期刊
CLINICAL CANCER RESEARCH
卷 27, 期 8, 页码 2301-2313出版社
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-20-3741
关键词
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类别
资金
- Pharmacyclics [16-PAF02251]
- University of Michigan Rogel Cancer Center Scholar award
- Weatherhall foundation
- hematological malignancy group of the University of Michigan through NCI CCSG [P30CA046592]
- Janssen RD
- [R01CA190384]
The study identified novel somatic BTK mutations in a small percentage of follicular lymphoma cases, demonstrating that these mutants destabilize the BTK protein and can induce an exaggerated AKT phosphorylation phenotype. The mutations did not affect PLC gamma 2 phosphorylation, but led to increased AKT phosphorylation following BCR cross-linking, with potential implications for targeted therapy development in follicular lymphoma.
Purpose: On the basis of the recent discovery of mutations in Bruton tyrosine kinase (BTK) in follicular lymphoma, we studied their functional properties. Experimental Design: We identified novel somatic BTK mutations in 7% of a combined total of 139 follicular lymphoma and 11 transformed follicular lymphoma cases, none of which had received prior treatment with B-cell receptor (BCR) targeted drugs. We reconstituted wild-type (WT) and mutant BTK into various engineered lymphoma cell lines. We measured BCR-induced signal transduction events in engineered cell lines and primary human follicular lymphoma B cells. Results: We uncovered that all BTK mutants destabilized the BTK protein and some created BTK kinase-dead mutants. The phospholipase C gamma 2 (PLC gamma 2) is a substrate of BTK but the BTK mutants did not alter PLC gamma 2 phosphorylation. Instead, we discovered that BTK mutants induced an exaggerated AKT phosphorylation phenotype in anti-Ig-treated recombinant lymphoma cell lines. The short hairpin RNA-mediated knockdown of BTK expression in primary human nonmalignant lymph node-derived B cells resulted in strong anti-Ig-induced AKT activation, as did the degradation of BTK protein in cell lines using ibrutinib-based proteolysis targeting chimera. Finally, through analyses of primary human follicular lymphoma B cells carrying WT or mutant BTK, we detected elevated AKT phosphorylation following surface Ig crosslinking in all follicular lymphoma B cells, including all BTK-mutant follicular lymphoma. The augmented AKT phosphorylation following BCR cross-linking could be abrogated by pretreatment with a PI3K delta inhibitor. Conclusions: Altogether, our data uncover novel unexpected properties of follicular lymphoma-associated BTK mutations with direct implications for targeted therapy development in follicular lymphoma.
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