Y染色体缺失:新一代疾病预测和早期检测的生物标志物?

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Xihan Guo , Jianfei Li , Jinglun Xue , Michael Fenech , Xu Wang
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引用次数: 4

摘要

随着人类预期寿命的大幅增加,衰老是大多数慢性疾病的主要危险因素,迫切需要推进后基因组时代生物标志物的开发,用于疾病预测和早期检测(DPED)。Y染色体镶嵌缺失(Mosaic loss of Y chromosome, LOY)是指在受精卵后不同发育阶段及以后整个生命周期中获得的体细胞亚群中的Y染色体失配状态。多项基于大队列的流行病学研究发现,血细胞中的LOY是男性未来死亡率和各种疾病的重要危险因素。可以利用LOY分析的许多固有特征来增强其作为DPED的非侵入性,敏感,可靠,高通量生物标志物的用途。在此,我们回顾了LOY研究的新兴文献,并强调了将LOY作为基因组学驱动的DPED诊断的新型生物标志物的十大优势。同时,对目前该领域的局限性也进行了讨论。最后,我们确定了一些关于Y染色体分离不良后果的重要知识缺口,并提出了临床实施LOY之前需要采取的进一步步骤。综上所述,我们认为LOY作为DPED的生物标志物具有巨大的潜力,尽管在将其整合到医疗保健中被接受之前仍需要解决一些障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Loss of Y chromosome: An emerging next-generation biomarker for disease prediction and early detection?

As human life expectancy increases substantially and aging is the primary risk factor for most chronic diseases, there is an urgent need for advancing the development of post-genomic era biomarkers that can be used for disease prediction and early detection (DPED). Mosaic loss of Y chromosome (LOY) is the state of nullisomy Y in sub-groups of somatic cells acquired from different post-zygotic development stages and onwards throughout the lifespan. Multiple large-cohort based epidemiology studies have found that LOY in blood cells is a significant risk factor for future mortality and various diseases in males. Many features intrinsic to LOY analysis may be leveraged to enhance its use as a non-invasive, sensitive, reliable, high throughput-biomarker for DPED. Here, we review the emerging literatures in LOY studies and highlight ten strengths for using LOY as a novel biomarker for genomics-driven DPED diagnostics. Meanwhile, the current limitations in this area are also discussed. We conclude by identifying some important knowledge gaps regarding the consequences of malsegregation of the Y chromosome and propose further steps that are required before clinical implementation of LOY. Taken together, we think that LOY has substantial potential as a biomarker for DPED, despite some hurdles that still need to be addressed before its integration into healthcare becomes acceptable.

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来源期刊
CiteScore
12.20
自引率
1.90%
发文量
22
审稿时长
15.7 weeks
期刊介绍: The subject areas of Reviews in Mutation Research encompass the entire spectrum of the science of mutation research and its applications, with particular emphasis on the relationship between mutation and disease. Thus this section will cover advances in human genome research (including evolving technologies for mutation detection and functional genomics) with applications in clinical genetics, gene therapy and health risk assessment for environmental agents of concern.
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