Swiss Institute for Experimental Cancer Research, School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
Blood. 2018 May 24;131(21):2345-2356. doi: 10.1182/blood-2017-10-809210. Epub 2018 Mar 22.
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.
在弥漫性大 B 细胞淋巴瘤 (DLBCL) 中,B 细胞受体 (BCR) 的激活促进了多种致癌信号,这些信号对肿瘤增殖至关重要。抑制 BCR 下游靶点布鲁顿酪氨酸激酶 (BTK) 在仅一部分 DLBCL 患者中具有治疗效果。在这里,我们使用从 DLBCL 患者中分离出的淋巴瘤细胞来测量靶向治疗对 BCR 信号的影响,并预测反应。在对 BTK 抑制有抗性的淋巴瘤中,我们表明阻断 BTK 活性增强了肿瘤对 BCR 下游替代致癌信号的依赖性,导致 MYC 上调。为了完全消除 BCR 的活性,我们通过遗传和药理学抑制了 SRC 激酶 LYN、FYN 和 BLK 的活性,这些激酶负责 BCR 信号的传播。抑制这些激酶强烈减少了来自 DLBCL 患者的异种移植物和细胞系中的肿瘤生长,与它们的分子亚型无关,这推进了在广泛和多样化的 DLBCL 患者群体中成为相关治疗靶点的可能性。