Molecular Medicine, CEITEC Masaryk University, and.
Department of Internal Medicine, Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Blood. 2021 Sep 2;138(9):758-772. doi: 10.1182/blood.2020008101.
Recirculation of chronic lymphocytic leukemia (CLL) cells between the peripheral blood and lymphoid niches plays a critical role in disease pathophysiology, and inhibiting this process is one of the major mechanisms of action for B-cell receptor (BCR) inhibitors such as ibrutinib and idelalisib. Migration is a complex process guided by chemokine receptors and integrins. However, it remains largely unknown how CLL cells integrate multiple migratory signals while balancing survival in the peripheral blood and the decision to return to immune niches. Our study provided evidence that CXCR4/CD5 intraclonal subpopulations can be used to study the regulation of migration of CLL cells. We performed RNA profiling of CXCR4dimCD5bright vs CXCR4brightCD5dim CLL cells and identified differential expression of dozens of molecules with a putative function in cell migration. GRB2-associated binding protein 1 (GAB1) positively regulated CLL cell homing capacity of CXCR4brightCD5dim cells. Gradual GAB1 accumulation in CLL cells outside immune niches was mediated by FoxO1-induced transcriptional GAB1 activation. Upregulation of GAB1 also played an important role in maintaining basal phosphatidylinositol 3-kinase (PI3K) activity and the "tonic" AKT phosphorylation required to sustain the survival of resting CLL B cells. This finding is important during ibrutinib therapy, because CLL cells induce the FoxO1-GAB1-pAKT axis, which represents an adaptation mechanism to the inability to home to immune niches. We have demonstrated that GAB1 can be targeted therapeutically by novel GAB1 inhibitors, alone or in combination with BTK inhibition. GAB1 inhibitors induce CLL cell apoptosis, impair cell migration, inhibit tonic or BCR-induced AKT phosphorylation, and block compensatory AKT activity during ibrutinib therapy.
慢性淋巴细胞白血病 (CLL) 细胞在周围血液和淋巴组织龛之间的再循环在疾病发病机制中起着关键作用,抑制这一过程是布鲁顿酪氨酸激酶 (BTK) 抑制剂(如伊布替尼和idelalisib)等 B 细胞受体 (BCR) 抑制剂的主要作用机制之一。迁移是一个受趋化因子受体和整合素指导的复杂过程。然而,CLL 细胞如何整合多种迁移信号,同时平衡在外周血液中的存活和返回免疫龛的决定,在很大程度上仍然未知。我们的研究提供了证据,表明 CXCR4/CD5 克隆内亚群可用于研究 CLL 细胞迁移的调节。我们对 CXCR4dimCD5bright 与 CXCR4brightCD5dim CLL 细胞进行了 RNA 谱分析,鉴定出数十种具有细胞迁移潜在功能的分子的差异表达。GRB2 相关结合蛋白 1 (GAB1) 正向调节 CXCR4brightCD5dim 细胞的 CLL 细胞归巢能力。FoxO1 诱导的转录 GAB1 激活介导了 CLL 细胞在免疫龛外逐渐积累 GAB1。GAB1 的上调在维持静止 CLL B 细胞的基础磷脂酰肌醇 3-激酶 (PI3K) 活性和维持其存活所需的“基础”AKT 磷酸化中也起着重要作用。这一发现对于伊布替尼治疗很重要,因为 CLL 细胞诱导 FoxO1-GAB1-pAKT 轴,这是对无法归巢到免疫龛的适应机制。我们已经证明,GAB1 可以通过新型 GAB1 抑制剂单独或与 BTK 抑制联合进行治疗性靶向。GAB1 抑制剂诱导 CLL 细胞凋亡,抑制细胞迁移,抑制基础或 BCR 诱导的 AKT 磷酸化,并在伊布替尼治疗期间阻断代偿性 AKT 活性。