1] Department of Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA [2] The University of Queensland Diamantina Institute, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
Oncogene. 2013 Oct;32(40):4727-36. doi: 10.1038/onc.2012.616. Epub 2013 Jan 14.
One form of chromosome instability (CIN), the recurrent missegregation of whole chromosomes during cell division (W-CIN), leads to aneuploidy. Although W-CIN is a hallmark of most cancers, mutations in genes involved in chromosome segregation are exceedingly rare. We discuss an oncogene-induced mitotic stress model that provides a mechanistic framework to explain this paradox. We also review the tumor-promoting and tumor-suppressing consequences of W-CIN. Importantly, we do this in the context of cancer as a complex systemic disease, rather than as a simple linearly progressing disorder that arises from a single abnormal cell population. Accordingly, we highlight the often neglected effects of W-CIN on key non-cell-autonomous entities, such as the immune system and the tumor microenvironment. Distinct tissue-specific susceptibilities to W-CIN-induced tumorigenesis and the clinical implications of W-CIN are also discussed.
一种染色体不稳定性(CIN)形式,即细胞分裂过程中整条染色体的反复错误分离(W-CIN),导致非整倍体。尽管 W-CIN 是大多数癌症的标志,但涉及染色体分离的基因发生突变极为罕见。我们讨论了一个致癌基因诱导的有丝分裂应激模型,该模型提供了一个机制框架来解释这一悖论。我们还回顾了 W-CIN 的肿瘤促进和肿瘤抑制后果。重要的是,我们是在癌症作为一种复杂的系统性疾病的背景下这样做的,而不是作为一种简单的线性进展性疾病,这种疾病源于单个异常细胞群体。因此,我们强调了 W-CIN 对免疫系统和肿瘤微环境等关键非细胞自主实体的经常被忽视的影响。还讨论了 W-CIN 诱导的肿瘤发生的不同组织特异性易感性和 W-CIN 的临床意义。