Zhou Jianbiao, Chng Wee-Joo
Cancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore 117599, Singapore;; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore.
Cancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore 117599, Singapore;; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore;; Department of Hematology-Oncology, National University Cancer Institute of Singapore (NCIS), The National University Health System (NUHS), Singapore 119228, Singapore.
Stem Cell Investig. 2017 Feb 9;4:6. doi: 10.21037/sci.2017.01.06. eCollection 2017.
The spliceosome, the cellular splicing machinery, regulates RNA splicing of messenger RNA precursors (pre-mRNAs) into maturation of protein coding RNAs. Recurrent mutations and copy number changes in genes encoding spliceosomal proteins and splicing regulatory factors have tumor promoting or suppressive functions in hematological malignancies, as well as some other cancers. Leukemia stem cell (LSC) populations, although rare, are essential contributors of treatment failure and relapse. Recent researches have provided the compelling evidence that link the erratic spicing activity to the LSC phenotype in acute myeloid leukemia (AML). In this article, we describe the diverse roles of aberrant splicing in hematological malignancies, particularly in AML and their contributions to the characteristics of LSC. We review these promising strategies to exploit the addiction of aberrant spliceosomal machinery for anti-leukemic therapy with aim to eradicate LSC. However, given the complexity and plasticity of spliceosome and not fully known functions of splicing in cancer, the challenges facing the development of the therapeutic strategies targeting RAN splicing are highlighted and future directions are discussed too.
剪接体,即细胞内的剪接机制,负责将信使核糖核酸前体(前体mRNA)进行RNA剪接,使其成熟为蛋白质编码RNA。编码剪接体蛋白和剪接调节因子的基因中反复出现的突变和拷贝数变化,在血液系统恶性肿瘤以及其他一些癌症中具有促肿瘤或抑肿瘤功能。白血病干细胞(LSC)群体虽然罕见,但却是治疗失败和复发的重要原因。最近的研究提供了令人信服的证据,将急性髓系白血病(AML)中不稳定的剪接活性与LSC表型联系起来。在本文中,我们描述了异常剪接在血液系统恶性肿瘤,特别是在AML中的多种作用,以及它们对LSC特征的影响。我们综述了这些利用异常剪接体机制成瘾进行抗白血病治疗的有前景的策略,旨在根除LSC。然而,鉴于剪接体的复杂性和可塑性以及剪接在癌症中尚未完全明确的功能,本文强调了针对RAN剪接的治疗策略开发所面临的挑战,并讨论了未来的方向。