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细胞衰老调控带来的治疗机遇。

Therapeutic Opportunities Presented by Modulation of Cellular Senescence.

作者信息

Faragher Richard G A, Heidari Neda, Ostler Elizabeth L

机构信息

Huxley Building, School of Applied Sciences, University of Brighton, Brighton, UK.

The Royal Veterinary College, Hertfordshire, UK.

出版信息

Subcell Biochem. 2023;102:175-193. doi: 10.1007/978-3-031-21410-3_8.

Abstract

Cellular senescence is a permanent state of growth arrest coupled with profound changes in phenotype that can be triggered by multiple extrinsic or intrinsic stimuli. Senescence is a process-level example of the evolution of ageing mechanisms through antagonistic pleiotropy and plays a primary role in tumour suppression, although evidence is mounting for its involvement in other fundamental physiological processes. Evidence from human premature ageing diseases and from transgenic mice in which it is possible to specifically delete senescent cells is consistent with a model in which the accumulation of senescent cells through the life course is responsible for later life chronic disease and impairment. The removal of senescent cells or their reversion to a phenotypically benign state is thus an important emerging goal of translational medicine.Modern bioinformatic approaches based on text mining have compiled co-mentions of cell senescence and age-related diseases allowing an impartial ranking of the impairments most closely associated with this process. Following this schema, the evidence for the involvement of senescence in several highly ranked pathologies is reviewed, alongside potential methods for the ablation of senescent cells or their reversion to their primary phenotype with polyphenolics or inhibitors of p38 MAP kinase. Lastly, the potential for senescence to act as a barrier to the development of bioartificial organs designed to treat some of these conditions is discussed.

摘要

细胞衰老一种永久性生长停滞状态,伴有表型的深刻变化,可由多种外在或内在刺激引发。衰老是衰老机制通过拮抗多效性进化的一个过程层面的例子,在肿瘤抑制中起主要作用,尽管越来越多的证据表明其参与其他基本生理过程。来自人类早衰疾病和能够特异性清除衰老细胞的转基因小鼠的证据与一种模型一致,即衰老细胞在整个生命过程中的积累是导致晚年慢性疾病和功能障碍的原因。因此,清除衰老细胞或将其恢复到表型良性状态是转化医学一个重要的新目标。基于文本挖掘的现代生物信息学方法汇总了细胞衰老与年龄相关疾病的共同提及内容,从而能够对与该过程最密切相关的功能障碍进行公正排名。按照这种模式,本文综述了衰老参与几种排名靠前的病理学的证据,以及清除衰老细胞或将其恢复到原始表型的潜在方法,如使用多酚类物质或p38丝裂原活化蛋白激酶抑制剂。最后,本文讨论了衰老可能成为设计用于治疗其中一些病症的生物人工器官发展障碍的可能性。

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