Zhang Fangliang, Chen Liang
Hubei Key Laboratory of Cell Homeostasis, RNA Institute, College of Life Sciences, Wuhan University, Wuhan 430072, China.
Biomedicines. 2022 Aug 15;10(8):1972. doi: 10.3390/biomedicines10081972.
Splicing factors are frequently mutated in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). These mutations are presumed to contribute to oncogenic transformation, but the underlying mechanisms remain incompletely understood. While no specific treatment option is available for MDS/AML patients with spliceosome mutations, novel targeting strategies are actively explored, leading to clinical trials of small molecule inhibitors that target the spliceosome, DNA damage response pathway, and immune response pathway. Here, we review recent progress in mechanistic understanding of splicing factor mutations promoting disease progression and summarize potential therapeutic strategies, which, if successful, would provide clinical benefit to patients carrying splicing factor mutations.
剪接因子在骨髓增生异常综合征(MDS)和急性髓系白血病(AML)中经常发生突变。这些突变被认为促成了致癌转化,但其潜在机制仍未完全了解。虽然对于患有剪接体突变的MDS/AML患者没有特定的治疗选择,但正在积极探索新的靶向策略,从而开展针对剪接体、DNA损伤反应途径和免疫反应途径的小分子抑制剂的临床试验。在此,我们综述了对促进疾病进展的剪接因子突变的机制理解方面的最新进展,并总结了潜在的治疗策略,若这些策略成功,将为携带剪接因子突变的患者带来临床益处。