Escobar-Hoyos Luisa, Knorr Katherine, Abdel-Wahab Omar
Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
David M. Rubenstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Annu Rev Cancer Biol. 2019 Mar;3(1):167-185. doi: 10.1146/annurev-cancerbio-030617-050407. Epub 2018 Nov 28.
RNA splicing, the enzymatic process of removing segments of premature RNA to produce mature RNA, is a key mediator of proteome diversity and regulator of gene expression. Increased systematic sequencing of the genome and transcriptome of cancers has identified a variety of means by which RNA splicing is altered in cancer relative to normal cells. These findings, in combination with the discovery of recurrent change-of-function mutations in splicing factors in a variety of cancers, suggest that alterations in splicing are drivers of tumorigenesis. Greater characterization of altered splicing in cancer parallels increasing efforts to pharmacologically perturb splicing and early-phase clinical development of small molecules that disrupt splicing in patients with cancer. Here we review recent studies of global changes in splicing in cancer, splicing regulation of mitogenic pathways critical in cancer transformation, and efforts to therapeutically target splicing in cancer.
RNA剪接是一种去除前体RNA片段以产生成熟RNA的酶促过程,是蛋白质组多样性的关键调节因子和基因表达的调控者。对癌症基因组和转录组进行的系统测序增多,已确定了多种癌症中RNA剪接相对于正常细胞发生改变的方式。这些发现,再加上在多种癌症中发现剪接因子存在反复的功能改变突变,表明剪接改变是肿瘤发生的驱动因素。对癌症中剪接改变的进一步表征,与在药理学上干扰剪接的努力以及小分子在癌症患者中破坏剪接的早期临床开发不断增加相平行。在此,我们综述了近期关于癌症中剪接全局变化、对癌症转化至关重要的促有丝分裂途径的剪接调控,以及针对癌症剪接进行治疗的研究。