• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

老细胞,新把戏:衰老过程中的染色质结构

Old cells, new tricks: chromatin structure in senescence.

作者信息

Parry Aled John, Narita Masashi

机构信息

Li Ka Shing Centre, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, CB2 0RE, UK.

出版信息

Mamm Genome. 2016 Aug;27(7-8):320-31. doi: 10.1007/s00335-016-9628-9. Epub 2016 Mar 28.

DOI:10.1007/s00335-016-9628-9
PMID:27021489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4935760/
Abstract

Cellular senescence is a stable form of cell cycle arrest with roles in many pathophysiological processes including development, tissue repair, cancer, and aging. Senescence does not represent a single entity but rather a heterogeneous phenotype that depends on the trigger and cell type of origin. Such heterogeneous features include alterations to chromatin structure and epigenetic states. New technologies are beginning to unravel the distinct mechanisms regulating chromatin structure during senescence. Here, we describe the multiple levels of chromatin organization associated with senescence: global and focal, linear, and higher order.

摘要

细胞衰老 是一种稳定的细胞周期停滞形式,在许多病理生理过程中发挥作用,包括发育、组织修复、癌症和衰老。衰老并非单一实体,而是一种异质性表型,取决于触发因素和起源细胞类型。这种异质性特征包括染色质结构和表观遗传状态的改变。新技术正开始揭示衰老过程中调节染色质结构的不同机制。在此,我们描述与衰老相关的染色质组织的多个层面:全局和局部、线性和高阶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/05906e8fd71c/335_2016_9628_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/4d653053380b/335_2016_9628_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/46be1489929f/335_2016_9628_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/05906e8fd71c/335_2016_9628_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/4d653053380b/335_2016_9628_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/46be1489929f/335_2016_9628_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a248/4935760/05906e8fd71c/335_2016_9628_Fig3_HTML.jpg

相似文献

1
Old cells, new tricks: chromatin structure in senescence.老细胞,新把戏:衰老过程中的染色质结构
Mamm Genome. 2016 Aug;27(7-8):320-31. doi: 10.1007/s00335-016-9628-9. Epub 2016 Mar 28.
2
Heterochromatin and its relationship to cell senescence and cancer therapy.异染色质及其与细胞衰老和癌症治疗的关系。
Cell Cycle. 2007 Apr 1;6(7):784-9. doi: 10.4161/cc.6.7.4079. Epub 2007 Apr 27.
3
Molecular Aspects of Senescence and Organismal Ageing-DNA Damage Response, Telomeres, Inflammation and Chromatin.衰老和机体老化的分子方面——DNA 损伤反应、端粒、炎症和染色质。
Int J Mol Sci. 2021 Jan 8;22(2):590. doi: 10.3390/ijms22020590.
4
Mapping H4K20me3 onto the chromatin landscape of senescent cells indicates a function in control of cell senescence and tumor suppression through preservation of genetic and epigenetic stability.将H4K20me3映射到衰老细胞的染色质景观上表明,它在通过维持遗传和表观遗传稳定性来控制细胞衰老和肿瘤抑制方面发挥作用。
Genome Biol. 2016 Jul 25;17(1):158. doi: 10.1186/s13059-016-1017-x.
5
The Chromatin Landscape of Cellular Senescence.细胞衰老的染色质景观
Trends Genet. 2016 Nov;32(11):751-761. doi: 10.1016/j.tig.2016.09.005. Epub 2016 Sep 28.
6
Alteration in the chromatin landscape during the DNA damage response: Continuous rotation of the gear driving cellular senescence and aging.在 DNA 损伤反应过程中染色质景观的改变:驱动细胞衰老和老化的齿轮连续旋转。
DNA Repair (Amst). 2023 Nov;131:103572. doi: 10.1016/j.dnarep.2023.103572. Epub 2023 Sep 17.
7
Large-scale chromatin reorganization reactivates placenta-specific genes that drive cellular aging.大规模染色质重排激活了驱动细胞衰老的胎盘特异性基因。
Dev Cell. 2022 Jun 6;57(11):1347-1368.e12. doi: 10.1016/j.devcel.2022.05.004. Epub 2022 May 24.
8
Dynamic 3D genome reorganization during senescence: defining cell states through chromatin.衰老过程中的动态三维基因组重组:通过染色质定义细胞状态
Cell Death Differ. 2025 Jan;32(1):9-15. doi: 10.1038/s41418-023-01197-y. Epub 2023 Aug 18.
9
Roles of chromatin and genome instability in cellular senescence and their relevance to ageing and related diseases.染色质和基因组不稳定性在细胞衰老中的作用及其与衰老和相关疾病的关系。
Nat Rev Mol Cell Biol. 2024 Dec;25(12):979-1000. doi: 10.1038/s41580-024-00775-3. Epub 2024 Oct 3.
10
Remodeling of chromatin structure in senescent cells and its potential impact on tumor suppression and aging.衰老细胞中染色质结构的重塑及其对肿瘤抑制和衰老的潜在影响。
Gene. 2007 Aug 1;397(1-2):84-93. doi: 10.1016/j.gene.2007.04.020. Epub 2007 May 1.

引用本文的文献

1
Interrogating the regulatory epigenome of cellular senescence.探究细胞衰老的调控表观基因组。
Cell Mol Life Sci. 2025 Aug 31;82(1):328. doi: 10.1007/s00018-025-05848-w.
2
Interplay between epigenetics, senescence and cellular redox metabolism in cancer and its therapeutic implications.癌症中表观遗传学、衰老与细胞氧化还原代谢之间的相互作用及其治疗意义。
Redox Biol. 2024 Dec;78:103441. doi: 10.1016/j.redox.2024.103441. Epub 2024 Nov 23.
3
NIH SenNet Consortium to map senescent cells throughout the human lifespan to understand physiological health.

本文引用的文献

1
Reorganization of chromosome architecture in replicative cellular senescence.有丝分裂细胞衰老过程中染色体结构的重组。
Sci Adv. 2016 Feb 5;2(2):e1500882. doi: 10.1126/sciadv.1500882. eCollection 2016 Feb.
2
Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan.天然存在的p16(Ink4a)阳性细胞会缩短健康寿命。
Nature. 2016 Feb 11;530(7589):184-9. doi: 10.1038/nature16932. Epub 2016 Feb 3.
3
SPOP E3 Ubiquitin Ligase Adaptor Promotes Cellular Senescence by Degrading the SENP7 deSUMOylase.SPOP E3泛素连接酶衔接蛋白通过降解SENP7去SUMO化酶促进细胞衰老。
NIH SenNet 联盟绘制人类整个生命周期中的衰老细胞图谱,以了解生理健康状况。
Nat Aging. 2022 Dec;2(12):1090-1100. doi: 10.1038/s43587-022-00326-5. Epub 2022 Dec 20.
4
Aging mechanisms-A perspective mostly from .衰老机制——主要来自……的观点
Adv Genet (Hoboken). 2020 Aug 10;1(1):e10026. doi: 10.1002/ggn2.10026. eCollection 2020 Dec.
5
Research on Werner Syndrome: Trends from Past to Present and Future Prospects.沃纳综合征研究:从过去到现在的趋势及未来展望。
Genes (Basel). 2022 Oct 6;13(10):1802. doi: 10.3390/genes13101802.
6
Inflammasome activation: from molecular mechanisms to autoinflammation.炎性小体激活:从分子机制到自身炎症
Clin Transl Immunology. 2022 Jul 7;11(7):e1404. doi: 10.1002/cti2.1404. eCollection 2022.
7
Translation of Cellular Senescence to Novel Therapeutics: Insights From Alternative Tools and Models.细胞衰老向新型疗法的转化:来自替代工具和模型的见解
Front Aging. 2022 Jun 1;3:828058. doi: 10.3389/fragi.2022.828058. eCollection 2022.
8
The methyltransferase enzymes KMT2D, SETD1B, and ASH1L are key mediators of both metabolic and epigenetic changes during cellular senescence.甲基转移酶酶 KMT2D、SETD1B 和 ASH1L 是细胞衰老过程中代谢和表观遗传变化的关键介质。
Mol Biol Cell. 2022 May 1;33(5):ar36. doi: 10.1091/mbc.E20-08-0523. Epub 2022 Feb 23.
9
Cellular Senescence: Mechanisms and Therapeutic Potential.细胞衰老:机制与治疗潜力
Biomedicines. 2021 Nov 25;9(12):1769. doi: 10.3390/biomedicines9121769.
10
FGF-2 induces a failure of cell cycle progression in cells harboring amplified K-Ras, revealing new insights into oncogene-induced senescence.FGF-2 诱导携带扩增 K-Ras 的细胞周期停滞,揭示了致癌基因诱导衰老的新见解。
Mol Omics. 2021 Oct 11;17(5):725-739. doi: 10.1039/d1mo00019e.
Cell Rep. 2015 Nov 10;13(6):1183-1193. doi: 10.1016/j.celrep.2015.09.083. Epub 2015 Oct 29.
4
Autophagy mediates degradation of nuclear lamina.自噬介导核纤层的降解。
Nature. 2015 Nov 5;527(7576):105-9. doi: 10.1038/nature15548. Epub 2015 Oct 28.
5
Autophagy-mediated degradation of nuclear envelope proteins during oncogene-induced senescence.癌基因诱导衰老过程中自噬介导的核膜蛋白降解
Carcinogenesis. 2015 Nov;36(11):1263-74. doi: 10.1093/carcin/bgv124. Epub 2015 Sep 8.
6
The expanding territories of condensin II.凝聚素II不断扩大的作用范围。
Cell Cycle. 2015;14(17):2723-4. doi: 10.1080/15384101.2015.1063356.
7
A novel role for the condensin II complex in cellular senescence.凝聚素II复合物在细胞衰老中的新作用。
Cell Cycle. 2015;14(13):2160-70. doi: 10.1080/15384101.2015.1049778.
8
BubR1 kinase: protection against aneuploidy and premature aging.BubR1 激酶:防止非整倍体和早衰。
Trends Mol Med. 2015 Jun;21(6):364-72. doi: 10.1016/j.molmed.2015.04.003. Epub 2015 May 8.
9
Reconfiguration of DNA methylation in aging.衰老过程中DNA甲基化的重新配置。
Mech Ageing Dev. 2015 Nov;151:60-70. doi: 10.1016/j.mad.2015.02.002. Epub 2015 Feb 20.
10
Global reorganization of the nuclear landscape in senescent cells.衰老细胞中核格局的全局重组。
Cell Rep. 2015 Feb 3;10(4):471-83. doi: 10.1016/j.celrep.2014.12.055. Epub 2015 Jan 29.