Functional Genetics Section, Genetics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Mol Carcinog. 2020 Dec;59(12):1343-1361. doi: 10.1002/mc.23260. Epub 2020 Oct 12.
The year 2021 marks the 20th anniversary of the first publications reporting the discovery of the gene silencing mechanism, RNA interference (RNAi) in mammalian cells. Along with the many studies that delineated the proteins and substrates that form the RNAi pathway, this finding changed our understanding of the posttranscriptional regulation of mammalian gene expression. Furthermore, the development of methods that exploited the RNAi pathway began the technological revolution that eventually enabled the interrogation of mammalian gene function-from a single gene to the whole genome-in only a few days. The needs of the cancer research community have driven much of this progress. In this perspective, we highlight milestones in the development and application of RNAi-based methods to study carcinogenesis. We discuss how RNAi-based functional genetic analysis of exemplar tumor suppressors and oncogenes furthered our understanding of cancer initiation and progression and explore how such studies formed the basis of genome-wide scale efforts to identify cancer or cancer-type specific vulnerabilities, including studies conducted in vivo. Furthermore, we examine how RNAi technologies have revealed new cancer-relevant molecular targets and the implications for cancer of the first RNAi-based drugs. Finally, we discuss the future of functional genetic analysis, highlighting the increasing availability of complementary approaches to analyze cancer gene function.
2021 年标志着首次报道在哺乳动物细胞中发现基因沉默机制 RNA 干扰 (RNAi) 的第一篇论文发表 20 周年。随着许多阐明形成 RNAi 途径的蛋白质和底物的研究的出现,这一发现改变了我们对哺乳动物基因表达转录后调控的理解。此外,利用 RNAi 途径的方法的发展开始了技术革命,最终使人们能够在短短几天内对从单个基因到整个基因组的哺乳动物基因功能进行检测。癌症研究界的需求推动了这一进展的大部分发展。在这篇观点文章中,我们重点介绍了基于 RNAi 的方法在癌症发生学研究中的发展和应用的里程碑。我们讨论了基于 RNAi 的功能遗传分析如何促进我们对癌症起始和进展的理解,并探讨了此类研究如何为基于全基因组的识别癌症或癌症类型特异性脆弱性的努力奠定基础,包括在体内进行的研究。此外,我们研究了 RNAi 技术如何揭示新的与癌症相关的分子靶标,以及 RNAi 为药物治疗癌症带来的影响。最后,我们讨论了功能遗传分析的未来,强调了分析癌症基因功能的互补方法的日益普及。