| Literature DB >> 29567799 |
Elena Battistello1,2,3, Natalya Katanayeva1, Elie Dheilly1, Daniele Tavernari2,3, Maria C Donaldson1, Luca Bonsignore4, Margot Thome4, Amanda L Christie5, Mark A Murakami5, Olivier Michielin6,7,8, Giovanni Ciriello2,3, Vincent Zoete7,8,9, Elisa Oricchio1.
Abstract
In diffuse large B-cell lymphoma (DLBCL), activation of the B-cell receptor (BCR) promotes multiple oncogenic signals, which are essential for tumor proliferation. Inhibition of the Bruton's tyrosine kinase (BTK), a BCR downstream target, is therapeutically effective only in a subgroup of patients with DLBCL. Here, we used lymphoma cells isolated from patients with DLBCL to measure the effects of targeted therapies on BCR signaling and to anticipate response. In lymphomas resistant to BTK inhibition, we show that blocking BTK activity enhanced tumor dependencies from alternative oncogenic signals downstream of the BCR, converging on MYC upregulation. To completely ablate the activity of the BCR, we genetically and pharmacologically repressed the activity of the SRC kinases LYN, FYN, and BLK, which are responsible for the propagation of the BCR signal. Inhibition of these kinases strongly reduced tumor growth in xenografts and cell lines derived from patients with DLBCL independent of their molecular subtype, advancing the possibility to be relevant therapeutic targets in broad and diverse groups of DLBCL patients.Entities:
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Year: 2018 PMID: 29567799 PMCID: PMC5969377 DOI: 10.1182/blood-2017-10-809210
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113