Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Universitat Pompeu Fabra, Barcelona, Spain.
Nat Rev Clin Oncol. 2020 Aug;17(8):457-474. doi: 10.1038/s41571-020-0350-x. Epub 2020 Apr 17.
Removal of introns from messenger RNA precursors (pre-mRNA splicing) is an essential step for the expression of most eukaryotic genes. Alternative splicing enables the regulated generation of multiple mRNA and protein products from a single gene. Cancer cells have general as well as cancer type-specific and subtype-specific alterations in the splicing process that can have prognostic value and contribute to every hallmark of cancer progression, including cancer immune responses. These splicing alterations are often linked to the occurrence of cancer driver mutations in genes encoding either core components or regulators of the splicing machinery. Of therapeutic relevance, the transcriptomic landscape of cancer cells makes them particularly vulnerable to pharmacological inhibition of splicing. Small-molecule splicing modulators are currently in clinical trials and, in addition to splice site-switching antisense oligonucleotides, offer the promise of novel and personalized approaches to cancer treatment.
从信使 RNA 前体(pre-mRNA 剪接)中去除内含子是大多数真核基因表达的一个必要步骤。可变剪接使一个基因能够从一个基因产生多个 mRNA 和蛋白质产物。癌细胞在剪接过程中存在普遍的以及癌症类型特异性和亚型特异性的改变,这些改变可能具有预后价值,并有助于癌症进展的每一个标志,包括癌症免疫反应。这些剪接改变通常与编码剪接机制核心成分或调节剂的基因中的癌症驱动突变的发生有关。在治疗方面,癌细胞的转录组景观使它们特别容易受到剪接的药理学抑制。小分子剪接调节剂目前正在临床试验中,除了剪接位点转换反义寡核苷酸外,还为癌症治疗提供了新的和个性化的方法的希望。