Towards prevention of aneuploidy-associated cellular senescence and aging: more questions than answers?

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Micheline Kirsch-Volders , Michael Fenech
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引用次数: 0

Abstract

The aim of this review is to discuss how aneuploidy contributes to the aging process, and to identify plausible strategies for its prevention. After an overview of mechanisms leading to aneuploidy and the major features of cellular senescence, we discuss the link between (i) aneuploidy and cellular senescence; (ii) aneuploidy and aging; and (iii) cellular senescence and aging. We also consider (i) interactions between aneuploidy, micronuclei, cellular senescence and aging, (ii) the potential of nutritional treatments to prevent aneuploidy-associated senescence and aging, and (iii) knowledge and technological gaps. Evidence for a causal link between aneuploidy, senescence and aging is emerging. In vitro, aneuploidy accompanies the entry into cellular senescence and can itself induce senescence. How aneuploidy contributes in vivo to cellular senescence is less clear. Several routes depending on aneuploidy and/or senescence converge towards chronic inflammation, the major driver of unhealthy aging. Aneuploidy can induce the pro-inflammatory Senescence Associated Secretory Phenotype (SASP), either directly or as a result of micronucleus (MN) induction leading to leakage of DNA into the cytoplasm and triggering of the cGAS-STING pathway of innate immune response. A major difficulty in understanding the impact of aneuploidy on senescence and aging in vivo, results from the heterogeneity of cellular senescence in different tissues at the cytological and molecular level. Due to this complexity, there is at the present time no biomarker or biomarker combination characteristic for all types of senescent cells. In conclusion, a deeper understanding of the critical role aneuploidy plays in cellular senescence and aging is essential to devise practical strategies to protect human populations from aneuploidy-associated pathologies. We discuss emerging evidence, based on in vitro and in vivo studies, that adequate amounts of specific micronutrients are essential for prevention of aneuploidy in humans and that precise nutritional intervention may be essential to help avoid the scourge of aneuploidy-driven diseases.

预防与肥胖相关的细胞衰老:问题多于答案?
这篇综述的目的是讨论非整倍体如何促进衰老过程,并确定合理的预防策略。在概述了导致非整倍体的机制和细胞衰老的主要特征后,我们讨论了(i)非整倍性与细胞衰老之间的联系;(ii)非整倍体和衰老;以及(iii)细胞衰老和衰老。我们还考虑了(i)非整倍体、微核、细胞衰老和衰老之间的相互作用,(ii)预防非整倍性相关衰老和衰老的营养治疗潜力,以及(iii)知识和技术差距。非整倍体、衰老和衰老之间存在因果关系的证据正在出现。在体外,非整倍体伴随着进入细胞衰老,并且自身可以诱导衰老。非整倍体如何在体内促进细胞衰老尚不清楚。依赖于非整倍体和/或衰老的几种途径汇聚成慢性炎症,这是不健康衰老的主要驱动因素。非整倍体可直接或作为微核(MN)诱导的结果诱导促炎性衰老相关分泌表型(SASP),导致DNA泄漏到细胞质中并触发先天免疫反应的cGAS-STING途径。在体内理解非整倍体对衰老和衰老的影响的一个主要困难是,不同组织中细胞衰老在细胞学和分子水平上的异质性。由于这种复杂性,目前不存在所有类型衰老细胞的生物标志物或生物标志物组合特征。总之,深入了解非整倍体在细胞衰老和衰老中的关键作用,对于制定切实可行的策略来保护人类免受非整倍性相关疾病的影响至关重要。我们讨论了基于体外和体内研究的新证据,即足量的特定微量营养素对预防人类非整倍体至关重要,精确的营养干预可能对避免非整倍性疾病的祸害至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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