Computational Biology Program, Public Health Sciences Division and Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Nat Rev Cancer. 2023 Mar;23(3):135-155. doi: 10.1038/s41568-022-00541-7. Epub 2023 Jan 10.
Dysregulated RNA splicing is a molecular feature that characterizes almost all tumour types. Cancer-associated splicing alterations arise from both recurrent mutations and altered expression of trans-acting factors governing splicing catalysis and regulation. Cancer-associated splicing dysregulation can promote tumorigenesis via diverse mechanisms, contributing to increased cell proliferation, decreased apoptosis, enhanced migration and metastatic potential, resistance to chemotherapy and evasion of immune surveillance. Recent studies have identified specific cancer-associated isoforms that play critical roles in cancer cell transformation and growth and demonstrated the therapeutic benefits of correcting or otherwise antagonizing such cancer-associated mRNA isoforms. Clinical-grade small molecules that modulate or inhibit RNA splicing have similarly been developed as promising anticancer therapeutics. Here, we review splicing alterations characteristic of cancer cell transcriptomes, dysregulated splicing's contributions to tumour initiation and progression, and existing and emerging approaches for targeting splicing for cancer therapy. Finally, we discuss the outstanding questions and challenges that must be addressed to translate these findings into the clinic.
RNA 剪接失调是几乎所有肿瘤类型的分子特征。与癌症相关的剪接改变源于反复出现的突变和调节剪接催化和调控的反式作用因子表达的改变。与癌症相关的剪接失调可通过多种机制促进肿瘤发生,导致细胞增殖增加、细胞凋亡减少、迁移和转移潜能增强、化疗耐药和免疫逃避。最近的研究已经确定了特定的与癌症相关的异构体,它们在癌细胞转化和生长中发挥关键作用,并证明了纠正或拮抗这种与癌症相关的 mRNA 异构体的治疗益处。同样,已开发出具有临床应用前景的调节或抑制 RNA 剪接的临床级小分子作为有前途的抗癌治疗药物。在这里,我们回顾了癌细胞转录组中特征性的剪接改变、失调剪接对肿瘤起始和进展的贡献,以及针对癌症治疗的现有和新兴的剪接靶向方法。最后,我们讨论了将这些发现转化为临床实践所必须解决的突出问题和挑战。