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衰老过程中的 DNA 损伤反应。

DNA damage responses in ageing.

机构信息

Institute for Genome Stability in Ageing and Disease, Medical Faculty, University of Cologne, Joseph-Stelzmann-Strasse 26, 50931 Cologne, Germany.

Cologne Excellence Cluster for Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Center for Molecular Medicine Cologne (CMMC), University of Cologne, Joseph-Stelzmann-Strasse 26, 50931 Cologne, Germany.

出版信息

Open Biol. 2019 Nov 29;9(11):190168. doi: 10.1098/rsob.190168. Epub 2019 Nov 20.


DOI:10.1098/rsob.190168
PMID:31744423
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6893400/
Abstract

Ageing appears to be a nearly universal feature of life, ranging from unicellular microorganisms to humans. Longevity depends on the maintenance of cellular functionality, and an organism's ability to respond to stress has been linked to functional maintenance and longevity. Stress response pathways might indeed become therapeutic targets of therapies aimed at extending the healthy lifespan. Various progeroid syndromes have been linked to genome instability, indicating an important causal role of DNA damage accumulation in the ageing process and the development of age-related pathologies. Recently, non-cell-autonomous mechanisms including the systemic consequences of cellular senescence have been implicated in regulating organismal ageing. We discuss here the role of cellular and systemic mechanisms of ageing and their role in ageing-associated diseases.

摘要

衰老是生命的一个普遍特征,从单细胞微生物到人类都存在衰老现象。长寿取决于细胞功能的维持,而生物体应对压力的能力与功能维持和长寿有关。压力反应途径确实可能成为旨在延长健康寿命的治疗方法的治疗靶点。各种早衰综合征与基因组不稳定性有关,这表明 DNA 损伤积累在衰老过程和与年龄相关的病理发展中起着重要的因果作用。最近,包括细胞衰老的系统性后果在内的非细胞自主机制也被认为在调节机体衰老中起作用。在这里,我们讨论了衰老的细胞和系统机制及其在与衰老相关的疾病中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/592e/6893400/46c50f8a0636/rsob-9-190168-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/592e/6893400/67af4dd785fd/rsob-9-190168-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/592e/6893400/46c50f8a0636/rsob-9-190168-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/592e/6893400/67af4dd785fd/rsob-9-190168-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/592e/6893400/46c50f8a0636/rsob-9-190168-g2.jpg

相似文献

[1]
DNA damage responses in ageing.

Open Biol. 2019-11-20

[2]
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本文引用的文献

[1]
New Trend in Old-Age Mortality: Gompertzialization of Mortality Trajectory.

Gerontology. 2019-5-20

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EMBO J. 2019-2-8

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Proc Natl Acad Sci U S A. 2019-1-25

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Aging Cell. 2018-11-21

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Reactivation of RNA metabolism underlies somatic restoration after adult reproductive diapause in .

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Senolytics improve physical function and increase lifespan in old age.

Nat Med. 2018-7-9

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A PQM-1-Mediated Response Triggers Transcellular Chaperone Signaling and Regulates Organismal Proteostasis.

Cell Rep. 2018-6-26

[9]
Role of hypothalamus in aging and its underlying cellular mechanisms.

Mech Ageing Dev. 2018-5-2

[10]
Brain-gut communications via distinct neuroendocrine signals bidirectionally regulate longevity in .

Genes Dev. 2018-2-1

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