Altered RNA Processing in Cancer Pathogenesis and Therapy

被引:103
作者
Obeng, Esther A. [1 ]
Stewart, Connor [2 ]
Abdel-Wahab, Omar [2 ]
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, 332 N Lauderdale St, Memphis, TN 38105 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Human Oncol & Pathogenesis Program & Leukemia Ser, New York, NY 10065 USA
关键词
PRE-MESSENGER-RNA; FACTOR CAPER-ALPHA; SF3B1; MUTATIONS; ALTERNATIVE POLYADENYLATION; SELECTIVE DEGRADATION; SPLICING MACHINERY; SOMATIC MUTATIONS; DRIVER MUTATIONS; PHASE-II; SPLICEOSOME;
D O I
10.1158/2159-8290.CD-19-0399
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Major advances in our understanding of cancer pathogenesis and therapy have come from efforts to catalog genomic alterations in cancer. A growing number of large-scale genomic studies have uncovered mutations that drive cancer by perturbing cotranscriptional and post-transcriptional regulation of gene expression. These include alterations that affect each phase of RNA processing, including splicing, transport, editing, and decay of messenger RNA. The discovery of these events illuminates a number of novel therapeutic vulnerabilities generated by aberrant RNA processing in cancer, several of which have progressed to clinical development. Significance: There is increased recognition that genetic alterations affecting RNA splicing and polyadenylation are common in cancer and may generate novel therapeutic opportunities. Such mutations may occur within an individual gene or in RNA processing factors themselves, thereby influencing splicing of many downstream target genes. This review discusses the biological impact of these mutations on tumorigenesis and the therapeutic approaches targeting cells bearing these mutations.
引用
收藏
页码:1493 / 1510
页数:18
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