Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China; Sino-French Research Center for Life Sciences and Genomics, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Neoplasia. 2020 Sep;22(9):447-457. doi: 10.1016/j.neo.2020.06.004. Epub 2020 Jul 9.
The dysregulation of alternative splicing (AS) has emerged as a mechanism of acute myeloid leukemia (AML). However, the prognostic impact of AS events remains under-explored in AML. Here we report the prognostic value of AS events and associated splicing factors based on three datasets of AML patients. We defined the landscape of AS events in AML and identified 7033 AS events associated with the survival of AML patients. Based on these events, we further developed a composite 15 AS event-based prognostic signature, which was independent of the cytogenetic risk stratification and patient age, and showed a better performance than known gene expression signatures. More importantly, our new signature markedly improved the European LeukemiaNet (ELN) risk classification, indicating a broad applicability in the clinical management of AML. Furthermore, the splicing-regulatory network established the correlations between prognostic AS events and associated splicing factors. The finding was validated by CRISPR-based data, which indicated that the increased expression of RBM39 contributed to the higher exon inclusion of SETD5 and conferred a poor outcome. Together, AS events may serve as a novel assortment of prognosticators for AML and could refine the ELN risk stratification. The splicing regulatory network provides clues regarding the splicing factor-mediated mechanisms of AML.
剪接(AS)失调已成为急性髓系白血病(AML)的一种机制。然而,AS 事件的预后影响在 AML 中仍未得到充分探索。在此,我们基于三个 AML 患者数据集报告了 AS 事件和相关剪接因子的预后价值。我们定义了 AML 中的 AS 事件图谱,并确定了 7033 个与 AML 患者生存相关的 AS 事件。基于这些事件,我们进一步开发了一种基于 15 个 AS 事件的综合预后特征,该特征独立于细胞遗传学危险分层和患者年龄,并且比已知的基因表达特征表现出更好的性能。更重要的是,我们的新特征显著改善了欧洲白血病网络(ELN)的风险分类,表明其在 AML 的临床管理中有广泛的适用性。此外,剪接调控网络建立了预后 AS 事件与相关剪接因子之间的相关性。CRISPR 数据的验证表明,RBM39 表达增加导致 SETD5 的外显子包含增加,并导致不良预后。总之,AS 事件可能成为 AML 的一种新的预后标志物,可以细化 ELN 的风险分层。剪接调控网络提供了有关 AML 中剪接因子介导机制的线索。