Limoli Charles L
a Department of Radiation Oncology , University of California , Irvine , CA , USA.
Int J Radiat Biol. 2017 Oct;93(10):1177-1181. doi: 10.1080/09553002.2016.1277800. Epub 2017 Jan 26.
This brief historical perspective will highlight the many accomplishments of the late William 'Bill' Morgan, and how his laboratory during the mid-1990s shaped the field of genomic instability. Bill focused on the processes responsible for radiation-induced genomic instability, and while ionizing radiation was known to induce this phenomenon, the precise causes were poorly understood. Here we revisit Bill's unique approach to these problems, as he advocated the use of novel mammalian cell lines to tease apart the mechanisms responsible for destabilizing an otherwise stable nuclear genome.
Genomic instability is a multifaceted process posited to be the driving force behind multistep carcinogenesis. Bill used a variety of innovative techniques that ultimately refined our understanding of the causes and consequences of radiation-induced chromosomal instability and the role it played in cancer predisposition. The central concepts of genomic instability fit nicely with the mutator phenotype hypothesis proposed by Lawrence Loeb, both of which represent functionally similar frameworks for describing how genomic stability can be compromised. The field of genomic instability has since advanced considerably, and much of our current knowledge is due to the efforts of Bill Morgan.
这篇简短的历史回顾将着重介绍已故的威廉·“比尔”·摩根的诸多成就,以及他在20世纪90年代中期的实验室如何塑造了基因组不稳定性领域。比尔专注于研究辐射诱导基因组不稳定性的相关过程,虽然已知电离辐射会诱发这种现象,但确切原因却知之甚少。在此,我们重新审视比尔解决这些问题的独特方法,他主张使用新型哺乳动物细胞系来梳理导致原本稳定的核基因组不稳定的机制。
基因组不稳定性是一个多方面的过程,被认为是多步骤致癌作用背后的驱动力。比尔运用了多种创新技术,最终完善了我们对辐射诱导的染色体不稳定性的成因及后果以及它在癌症易感性中所起作用的理解。基因组不稳定性的核心概念与劳伦斯·洛布提出的突变体表型假说非常契合,这两者都代表了描述基因组稳定性如何受到损害的功能相似的框架。自那以后,基因组不稳定性领域取得了长足进展,我们目前的许多知识都归功于比尔·摩根的努力。