Follicular Lymphoma-associated BTK Mutations are Inactivating Resulting in Augmented AKT Activation

Clin Cancer Res. 2021 Apr 15;27(8):2301-2313. doi: 10.1158/1078-0432.CCR-20-3741. Epub 2021 Jan 8.

Abstract

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 (PLCγ2) is a substrate of BTK but the BTK mutants did not alter PLCγ2 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 crosslinking could be abrogated by pretreatment with a PI3Kδ 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.See related commentary by Afaghani and Taylor, p. 2123.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agammaglobulinaemia Tyrosine Kinase / genetics*
  • Agammaglobulinaemia Tyrosine Kinase / metabolism
  • Cell Line, Tumor
  • Class I Phosphatidylinositol 3-Kinases / antagonists & inhibitors
  • Class I Phosphatidylinositol 3-Kinases / metabolism
  • DNA Mutational Analysis
  • Gene Knockdown Techniques
  • HEK293 Cells
  • Humans
  • Loss of Function Mutation
  • Lymphoma, Follicular / genetics*
  • Lymphoma, Follicular / pathology
  • Mutagenesis, Site-Directed
  • Phospholipase C gamma / metabolism
  • Phosphorylation / drug effects
  • Phosphorylation / genetics
  • Primary Cell Culture
  • Protein Stability
  • Proto-Oncogene Proteins c-akt / metabolism*

Substances

  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CA protein, human
  • Agammaglobulinaemia Tyrosine Kinase
  • BTK protein, human
  • AKT1 protein, human
  • Proto-Oncogene Proteins c-akt
  • PLCG2 protein, human
  • Phospholipase C gamma