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本文引用的文献

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Endothelial cell senescence with aging in healthy humans: prevention by habitual exercise and relation to vascular endothelial function.健康人群中内皮细胞衰老与衰老的关系:习惯性运动的预防作用及其与血管内皮功能的关系
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Premature senescence of cardiac fibroblasts and atrial fibrosis in patients with atrial fibrillation.心房颤动患者心脏成纤维细胞过早衰老与心房纤维化
Oncotarget. 2017 Aug 3;8(35):57981-57990. doi: 10.18632/oncotarget.19853. eCollection 2017 Aug 29.
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Nox4 regulates the eNOS uncoupling process in aging endothelial cells.Nox4 调节衰老内皮细胞中的 eNOS 解偶联过程。
Free Radic Biol Med. 2017 Dec;113:26-35. doi: 10.1016/j.freeradbiomed.2017.09.010. Epub 2017 Sep 12.
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Identification of HSP90 inhibitors as a novel class of senolytics.鉴定热休克蛋白90(HSP90)抑制剂作为一类新型衰老细胞裂解剂。
Nat Commun. 2017 Sep 4;8(1):422. doi: 10.1038/s41467-017-00314-z.
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Hyperphosphatemia induces senescence in human endothelial cells by increasing endothelin-1 production.高磷血症通过增加内皮素-1 的产生诱导人内皮细胞衰老。
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p16(Ink4a) and senescence-associated β-galactosidase can be induced in macrophages as part of a reversible response to physiological stimuli.p16(Ink4a)和衰老相关β半乳糖苷酶可在巨噬细胞中被诱导产生,作为对生理刺激的可逆反应的一部分。
Aging (Albany NY). 2017 Aug 2;9(8):1867-1884. doi: 10.18632/aging.101268.
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Senescent cells: an emerging target for diseases of ageing.衰老细胞:衰老相关疾病的一个新靶点。
Nat Rev Drug Discov. 2017 Oct;16(10):718-735. doi: 10.1038/nrd.2017.116. Epub 2017 Jul 21.
8
Effect of renin-angiotensin system inhibitors on mortality in heart failure with preserved ejection fraction: a meta-analysis of observational cohort and randomized controlled studies.血管紧张素转换酶抑制剂或血管紧张素受体拮抗剂对射血分数保留心力衰竭患者死亡率的影响:一项观察性队列和随机对照研究的荟萃分析。
Heart Fail Rev. 2017 Nov;22(6):775-782. doi: 10.1007/s10741-017-9637-0.
9
Endothelial Senescence Contributes to Heart Failure With Preserved Ejection Fraction in an Aging Mouse Model.在衰老小鼠模型中,内皮细胞衰老促成射血分数保留的心力衰竭。
Circ Heart Fail. 2017 Jun;10(6). doi: 10.1161/CIRCHEARTFAILURE.116.003806.
10
A Novel Indication for Panobinostat as a Senolytic Drug in NSCLC and HNSCC.新型帕比司他可作为 NSCLC 和 HNSCC 的衰老细胞溶解剂
Sci Rep. 2017 May 15;7(1):1900. doi: 10.1038/s41598-017-01964-1.

衰老细胞:心血管疾病的治疗靶点。

Senescent cells: a therapeutic target for cardiovascular disease.

机构信息

Department of Biochemistry and Molecular Biology.

Department of Molecular Pharmacology and Experimental Therapeutics, and.

出版信息

J Clin Invest. 2018 Apr 2;128(4):1217-1228. doi: 10.1172/JCI95146.

DOI:10.1172/JCI95146
PMID:29608141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5873883/
Abstract

Cellular senescence, a major tumor-suppressive cell fate, has emerged from humble beginnings as an in vitro phenomenon into recognition as a fundamental mechanism of aging. In the process, senescent cells have attracted attention as a therapeutic target for age-related diseases, including cardiovascular disease (CVD), the leading cause of morbidity and mortality in the elderly. Given the aging global population and the inadequacy of current medical management, attenuating the health care burden of CVD would be transformative to clinical practice. Here, we review the evidence that cellular senescence drives CVD in a bimodal fashion by both priming the aged cardiovascular system for disease and driving established disease forward. Hence, the growing field of senotherapy (neutralizing senescent cells for therapeutic benefit) is poised to contribute to both prevention and treatment of CVD.

摘要

细胞衰老,一种主要的肿瘤抑制性细胞命运,已经从一个简单的体外现象发展成为衰老的基本机制。在这个过程中,衰老细胞作为与年龄相关疾病的治疗靶点引起了人们的关注,包括心血管疾病(CVD),这是老年人发病率和死亡率的主要原因。鉴于全球人口老龄化和当前医疗管理的不足,减轻 CVD 的医疗保健负担将对临床实践产生变革性的影响。在这里,我们回顾了细胞衰老以两种方式驱动 CVD 的证据,既为衰老的心血管系统疾病做好了准备,又推动了已确立的疾病的发展。因此,日益发展的衰老治疗学领域(中和衰老细胞以获得治疗益处)有望为 CVD 的预防和治疗做出贡献。