Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Program in Computational Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Cancer Res. 2020 Feb 1;80(3):367-374. doi: 10.1158/0008-5472.CAN-19-0924. Epub 2019 Nov 6.
The incidence of cancer, adjusted for secular trends, is directly related to age, and advanced chronologic age is one of the most significant risk factors for cancer. Organismal aging is associated with changes at the molecular, cellular, and tissue levels and is affected by both genetic and environmental factors. The specific mechanisms through which these age-associated molecular changes contribute to the increased risk of aging-related disease, such as cancer, are incompletely understood. DNA methylation, a prominent epigenetic mark, also changes over a lifetime as part of an "epigenetic aging" process. Here, we give an update and review of epigenetic aging, in particular, the phenomena of epigenetic drift and epigenetic clock, with regard to its implication in cancer etiology. We discuss the discovery of the DNA methylation-based biomarkers for biological tissue age and the construction of various epigenetic age estimators for human clinical outcomes and health/life span. Recent studies in various types of cancer point to the significance of epigenetic aging in tumorigenesis and its potential use for cancer risk prediction. Future studies are needed to assess the potential clinical impact of strategies focused on lowering cancer risk by preventing premature aging or promoting healthy aging.
癌症的发病率,经时间趋势校正后,与年龄直接相关,而高龄是癌症最重要的危险因素之一。机体衰老与分子、细胞和组织水平的变化有关,受遗传和环境因素的影响。这些与年龄相关的分子变化导致与衰老相关的疾病(如癌症)风险增加的具体机制尚不完全清楚。DNA 甲基化是一种重要的表观遗传标记,也是一生中作为“表观遗传衰老”过程的一部分发生变化的。在这里,我们更新并回顾了表观遗传衰老,特别是表观遗传漂移和表观遗传时钟的现象,及其在癌症病因学中的意义。我们讨论了基于 DNA 甲基化的生物组织年龄生物标志物的发现,以及用于人类临床结果和健康/寿命的各种表观遗传年龄估算器的构建。各种类型癌症的最新研究表明,表观遗传衰老在肿瘤发生中的重要性及其在癌症风险预测中的潜在用途。需要进一步的研究来评估通过预防过早衰老或促进健康衰老来降低癌症风险的策略的潜在临床影响。