• 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

衰老在癌症中的动态特性。

The dynamic nature of senescence in cancer.

机构信息

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health; Medical Department of Hematology, Oncology and Tumor Immunology, Virchow Campus, and Molekulares Krebsforschungszentrum, Berlin, Germany.

Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.

出版信息

Nat Cell Biol. 2019 Jan;21(1):94-101. doi: 10.1038/s41556-018-0249-2. Epub 2019 Jan 2.

DOI:10.1038/s41556-018-0249-2
PMID:30602768
Abstract

Cellular senescence is implicated in physiological and pathological processes spanning development, wound healing, age-related decline in organ functions and cancer. Here, we discuss cell-autonomous and non-cell-autonomous properties of senescence in the context of tumour formation and anticancer therapy, and characterize these properties, such as reprogramming into stemness, tissue remodelling and immune crosstalk, as far more dynamic than suggested by the common view of senescence as an irreversible, static condition.

摘要

细胞衰老与贯穿发育、伤口愈合、与年龄相关的器官功能下降和癌症等生理和病理过程有关。在这里,我们讨论了衰老在肿瘤形成和抗癌治疗背景下的自主和非自主特性,并将这些特性(如重新编程为干性、组织重塑和免疫串扰)描述为比衰老作为一种不可逆的、静态状态的常见观点所暗示的更为动态。

相似文献

1
The dynamic nature of senescence in cancer.衰老在癌症中的动态特性。
Nat Cell Biol. 2019 Jan;21(1):94-101. doi: 10.1038/s41556-018-0249-2. Epub 2019 Jan 2.
2
Oncogenic senescence: a multi-functional perspective.致癌性衰老:多维度视角
Oncotarget. 2017 Apr 18;8(16):27661-27672. doi: 10.18632/oncotarget.15742.
3
Cellular Senescence: What, Why, and How.细胞衰老:是什么、为何以及如何发生。
Wounds. 2017 Jun;29(6):168-174.
4
Cellular senescence: a promising strategy for cancer therapy.细胞衰老:癌症治疗的一种有前途的策略。
BMB Rep. 2019 Jan;52(1):35-41. doi: 10.5483/BMBRep.2019.52.1.294.
5
Cellular senescence in tissue repair: every cloud has a silver lining.组织修复中的细胞衰老:黑暗中总有一线光明。
Int J Dev Biol. 2018;62(6-7-8):591-604. doi: 10.1387/ijdb.180081my.
6
ATM in senescence.衰老过程中的ATM
Oncotarget. 2015 Jun 20;6(17):14729-30. doi: 10.18632/oncotarget.4411.
7
Senescence-associated extracellular vesicle release plays a role in senescence-associated secretory phenotype (SASP) in age-associated diseases.衰老相关细胞外囊泡的释放在与年龄相关的疾病中的衰老相关分泌表型 (SASP) 中起作用。
J Biochem. 2021 Mar 5;169(2):147-153. doi: 10.1093/jb/mvaa109.
8
Cellular Senescence: Aging, Cancer, and Injury.细胞衰老:衰老、癌症和损伤。
Physiol Rev. 2019 Apr 1;99(2):1047-1078. doi: 10.1152/physrev.00020.2018.
9
Role of Sirtuin1-p53 regulatory axis in aging, cancer and cellular reprogramming.Sirtuin1-p53 调节轴在衰老、癌症和细胞重编程中的作用。
Ageing Res Rev. 2018 May;43:64-80. doi: 10.1016/j.arr.2018.02.004. Epub 2018 Feb 21.
10
Cellular Senescence: The Sought or the Unwanted?细胞衰老:是追求还是逃避?
Trends Mol Med. 2018 Oct;24(10):871-885. doi: 10.1016/j.molmed.2018.08.002. Epub 2018 Aug 25.

引用本文的文献

1
Immunosenescence and cancer: molecular hallmarks, tumor microenvironment remodeling, and age-specific immunotherapy challenges.免疫衰老与癌症:分子特征、肿瘤微环境重塑及特定年龄的免疫治疗挑战
J Hematol Oncol. 2025 Aug 22;18(1):81. doi: 10.1186/s13045-025-01735-w.
2
The senescence-inhibitory p53 isoform Δ133p53α: enhancing cancer immunotherapy and exploring novel therapeutic approaches for senescence-associated diseases.衰老抑制性p53亚型Δ133p53α:增强癌症免疫治疗并探索衰老相关疾病的新型治疗方法。
Geroscience. 2025 Aug 6. doi: 10.1007/s11357-025-01819-y.
3
Extracellular vesicles from ovarian cancer cells induce senescent lipid-laden macrophages to facilitate omental metastasis.

本文引用的文献

1
PTBP1-Mediated Alternative Splicing Regulates the Inflammatory Secretome and the Pro-tumorigenic Effects of Senescent Cells.PTBP1 介导的可变剪接调节衰老细胞的炎症分泌组和促肿瘤效应。
Cancer Cell. 2018 Jul 9;34(1):85-102.e9. doi: 10.1016/j.ccell.2018.06.007.
2
UnSASPing Senescence: Unmasking Tumor Suppression?去衰老化:揭开肿瘤抑制?
Cancer Cell. 2018 Jul 9;34(1):6-8. doi: 10.1016/j.ccell.2018.06.009.
3
Regulation of Cellular Senescence by Polycomb Chromatin Modifiers through Distinct DNA Damage- and Histone Methylation-Dependent Pathways.
卵巢癌细胞释放的细胞外囊泡可诱导衰老的脂质负载巨噬细胞,促进大网膜转移。
J Nanobiotechnology. 2025 Jul 26;23(1):540. doi: 10.1186/s12951-025-03612-7.
4
Modelling the ageing dependence of cancer evolutionary trajectories.模拟癌症进化轨迹的衰老依赖性。
Nat Rev Cancer. 2025 Jul 10. doi: 10.1038/s41568-025-00838-3.
5
ACSL5 regulated acetyl-CoA to promote bladder cancer cellular senescence via 53BP1 acetylation.ACSL5通过53BP1乙酰化调节乙酰辅酶A以促进膀胱癌细胞衰老。
Oncogene. 2025 Jul 1. doi: 10.1038/s41388-025-03474-1.
6
Δ133p53α-mediated inhibition of astrocyte senescence and neurotoxicity as a possible therapeutic approach for neurodegenerative diseases.Δ133p53α介导的星形胶质细胞衰老和神经毒性抑制作为神经退行性疾病的一种可能治疗方法。
Neuroscience. 2025 Jun 14;580:54-61. doi: 10.1016/j.neuroscience.2025.06.031.
7
Integrative Bioinformatic Analysis of Cellular Senescence Genes in Ovarian Cancer: Molecular Subtyping, Prognostic Risk Stratification, and Chemoresistance Prediction.卵巢癌中细胞衰老基因的综合生物信息学分析:分子亚型、预后风险分层及化疗耐药预测
Biomedicines. 2025 Apr 4;13(4):877. doi: 10.3390/biomedicines13040877.
8
SASP Modulation for Cellular Rejuvenation and Tissue Homeostasis: Therapeutic Strategies and Molecular Insights.用于细胞年轻化和组织稳态的SASP调节:治疗策略与分子见解
Cells. 2025 Apr 17;14(8):608. doi: 10.3390/cells14080608.
9
Modelling the spatiotemporal dynamics of senescent cells in wound healing, chronic wounds, and fibrosis.模拟衰老细胞在伤口愈合、慢性伤口和纤维化中的时空动态。
PLoS Comput Biol. 2025 Apr 15;21(4):e1012298. doi: 10.1371/journal.pcbi.1012298. eCollection 2025 Apr.
10
Regulation of nucleotide excision repair by wild-type HRAS signaling in head and neck cancer.头颈部癌中野生型HRAS信号传导对核苷酸切除修复的调控
Cancer Gene Ther. 2025 Apr 12. doi: 10.1038/s41417-025-00902-y.
多梳染色质修饰物通过不同的 DNA 损伤和组蛋白甲基化依赖途径调控细胞衰老。
Cell Rep. 2018 Mar 27;22(13):3480-3492. doi: 10.1016/j.celrep.2018.03.002.
4
Targeting the Senescence-Overriding Cooperative Activity of Structurally Unrelated H3K9 Demethylases in Melanoma.靶向黑色素瘤中结构不相关的 H3K9 去甲基酶的衰老超越协同活性。
Cancer Cell. 2018 Feb 12;33(2):322-336.e8. doi: 10.1016/j.ccell.2018.01.002.
5
Senescence-associated reprogramming promotes cancer stemness.衰老相关重编程促进癌症干性。
Nature. 2018 Jan 4;553(7686):96-100. doi: 10.1038/nature25167. Epub 2017 Dec 20.
6
Coupling shRNA screens with single-cell RNA-seq identifies a dual role for mTOR in reprogramming-induced senescence.将短发夹RNA(shRNA)筛选与单细胞RNA测序相结合,揭示了雷帕霉素靶蛋白(mTOR)在重编程诱导的衰老中的双重作用。
Genes Dev. 2017 Oct 15;31(20):2085-2098. doi: 10.1101/gad.297796.117. Epub 2017 Nov 14.
7
High-Throughput Functional Genetic and Compound Screens Identify Targets for Senescence Induction in Cancer.高通量功能遗传和化合物筛选鉴定诱导肿瘤衰老的靶点。
Cell Rep. 2017 Oct 17;21(3):773-783. doi: 10.1016/j.celrep.2017.09.085.
8
Cytoplasmic chromatin triggers inflammation in senescence and cancer.细胞质染色质在衰老和癌症中引发炎症。
Nature. 2017 Oct 19;550(7676):402-406. doi: 10.1038/nature24050. Epub 2017 Oct 4.
9
Unmasking Transcriptional Heterogeneity in Senescent Cells.揭示衰老细胞中的转录异质性。
Curr Biol. 2017 Sep 11;27(17):2652-2660.e4. doi: 10.1016/j.cub.2017.07.033. Epub 2017 Aug 30.
10
Targeting cellular senescence prevents age-related bone loss in mice.靶向细胞衰老可预防小鼠的年龄相关性骨质流失。
Nat Med. 2017 Sep;23(9):1072-1079. doi: 10.1038/nm.4385. Epub 2017 Aug 21.