Doherty Aoife, Kernogitski Yelena, Kulminski Alexander M, Pedro de Magalhães João
Integrative Genomics of Ageing Group, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, L7 8TX, United Kingdom.
Biodemography of Aging Research Unit (BARU), Social Science Research Institute, Duke University, Durham, NC 27708, USA.
Aging (Albany NY). 2017 Oct 20;9(10):2117-2136. doi: 10.18632/aging.101305.
The World Health Organization predicts that the proportion of the world's population over 60 will almost double from 12% to 22% between 2015 and 2050. Ageing is the biggest risk factor for cancer, which is a leading cause of deaths worldwide. Unfortunately, research describing how genetic variants affect cancer progression commonly neglects to account for the ageing process. Herein is the first systematic analysis that combines a large longitudinal data set with a targeted candidate gene approach to examine the effect of genetic variation on survival as a function of age in cancer patients. Survival was significantly decreased in individuals with heterozygote or rare homozygote (i.e. variant) genotypes compared to those with a common homozygote genotype (i.e. wild type) for two single nucleotide polymorphisms (rs11574358 and rs4147918), one gene () and one pathway (FoxO signalling) in an age-dependent manner. All identified genes and pathways have previously been associated with ageing and cancer. These observations demonstrate that there are ageing-related genetic elements that differentially affect mortality in cancer patients in an age-dependent manner. Understanding the genetic determinants affecting prognosis differently with age will be invaluable to develop age-specific prognostic biomarkers and personalized therapies that may improve clinical outcomes for older individuals.
世界卫生组织预测,2015年至2050年间,全球60岁以上人口的比例将几乎翻倍,从12%增至22%。衰老是癌症的最大风险因素,癌症是全球主要死因之一。不幸的是,描述基因变异如何影响癌症进展的研究通常忽略了衰老过程。本文首次进行了系统分析,将大型纵向数据集与靶向候选基因方法相结合,以研究基因变异对癌症患者生存的影响如何随年龄变化。对于两个单核苷酸多态性(rs11574358和rs4147918)、一个基因()和一条信号通路(FoxO信号通路),与具有常见纯合子基因型(即野生型)的个体相比,杂合子或罕见纯合子(即变异型)基因型个体的生存率随年龄增长显著降低。所有已确定的基因和信号通路此前均与衰老和癌症相关。这些观察结果表明,存在与衰老相关的基因元件,它们以年龄依赖的方式对癌症患者的死亡率产生不同影响。了解随年龄变化对预后有不同影响的遗传决定因素,对于开发可能改善老年个体临床结局的年龄特异性预后生物标志物和个性化疗法将具有重要价值。