Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano (PN), Italy.
Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano (PN), Italy; University of Trieste, Trieste, Italy.
Haematologica. 2021 Dec 1;106(12):3125-3135. doi: 10.3324/haematol.2020.261891.
Chronic lymphocytic leukemia (CLL) is characterized by a low CD20 expression, in part explained by an epigenetic-driven downregulation triggered by mutations of the NOTCH1 gene. In the present study, by taking advantage of a wide and well-characterized CLL cohort (n=537), we demonstrate that CD20 expression is downregulated in SF3B1-mutated CLL in an extent similar to NOTCH1-mutated CLL. In fact, SF3B1-mutated CLL cells show common features with NOTCH1-mutated CLL cells, including a gene expression profile enriched of NOTCH1-related gene sets and elevated expression of the active intracytoplasmic NOTCH1. Activation of the NOTCH1 signaling and down-regulation of surface CD20 in SF3B1-mutated CLL cells correlate with over-expression of an alternatively spliced form of DVL2, a component of the Wnt pathway and negative regulator of the NOTCH1 pathway. These findings are confirmed by separately analyzing the CD20-dim and CD20-bright cell fractions from SF3B1-mutated cases as well as by DVL2 knock-out experiments in CLL-like cell models. Altogether, the clinical and biological features that characterize NOTCH1-mutated CLL may also be recapitulated in SF3B1-mutated CLL, contributing to explain the poor prognosis of this CLL subset and providing the rationale for expanding novel agents-based therapies to SF3B1-mutated CLL.
慢性淋巴细胞白血病(CLL)的特征是 CD20 表达水平低,部分原因是 NOTCH1 基因突变引发的表观遗传驱动下调。在本研究中,通过利用广泛且特征良好的 CLL 队列(n=537),我们证明 SF3B1 突变的 CLL 中 CD20 的表达下调程度与 NOTCH1 突变的 CLL 相似。事实上,SF3B1 突变的 CLL 细胞与 NOTCH1 突变的 CLL 细胞具有共同特征,包括富含 NOTCH1 相关基因集的基因表达谱和细胞内活跃的 NOTCH1 的表达上调。SF3B1 突变的 CLL 细胞中 NOTCH1 信号的激活和表面 CD20 的下调与 DVL2 的一种剪接变体的过表达相关,DVL2 是 Wnt 途径的一个组成部分,也是 NOTCH1 途径的负调节剂。这些发现通过分别分析 SF3B1 突变病例中的 CD20 暗淡和 CD20 明亮细胞亚群以及在 CLL 样细胞模型中进行 DVL2 敲除实验得到了证实。总之,NOTCH1 突变的 CLL 所具有的临床和生物学特征也可能在 SF3B1 突变的 CLL 中重现,这有助于解释该 CLL 亚组的不良预后,并为将基于新型药物的治疗方法扩展到 SF3B1 突变的 CLL 提供了依据。