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How to Slow down the Ticking Clock: Age-Associated Epigenetic Alterations and Related Interventions to Extend Life Span

Medicine and Health

How to Slow down the Ticking Clock: Age-Associated Epigenetic Alterations and Related Interventions to Extend Life Span

A. Galow and S. Peleg

Discover groundbreaking insights on how epigenetic changes influence aging and related diseases, delivered by researchers Anne-Marie Galow and Shahaf Peleg. This review sheds light on the intricate connections between epigenetics, transcriptional shifts, and metabolic pathways, revealing potential biomarkers and therapeutic approaches for age-related disorders.

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~3 min • Beginner • English
Abstract
Epigenetic alterations pose one major hallmark of organismal aging. Here, we provide an overview on recent findings describing the epigenetic changes that arise during aging and in related maladies such as neurodegeneration and cancer. Specifically, we focus on alterations of histone modifications and DNA methylation and illustrate the link with metabolic pathways. Age-related epigenetic, transcriptional and metabolic deregulations are highly interconnected, which renders dissociating cause and effect complicated. However, growing amounts of evidence support the notion that aging is not only accompanied by epigenetic alterations, but also at least in part induced by those. DNA methylation clocks emerged as a tool to objectively determine biological aging and turned out as a valuable source in search of factors positively and negatively impacting human life span. Moreover, specific epigenetic signatures can be used as biomarkers for age-associated disorders or even as targets for therapeutic approaches, as will be covered in this review. Finally, we summarize recent potential intervention strategies that target epigenetic mechanisms to extend healthy life span and provide an outlook on future developments in the field of longevity research.
Publisher
Cells
Published On
Oct 26, 2022
Authors
Anne-Marie Galow, Shahaf Peleg
Tags
epigenetics
aging
DNA methylation
neurodegeneration
cancer
biological aging
therapeutic strategies
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