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肝脏衰老的生物学机制和新兴治疗干预措施。

The biological mechanism and emerging therapeutic interventions of liver aging.

机构信息

Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.

NHC Key Laboratory of Combined Multi-organ Transplantation, Hangzhou 310003, China.

出版信息

Int J Biol Sci. 2024 Jan 1;20(1):280-295. doi: 10.7150/ijbs.87679. eCollection 2024.

Abstract

Research on liver aging has become prominent and has attracted considerable interest in uncovering the mechanism and therapeutic targets of aging to expand lifespan. In addition, multi-omics studies are widely used to perform further mechanistic investigations on liver aging. In this review, we illustrate the changes that occur with aging in the liver, present the current models of liver aging, and emphasize existing multi-omics studies on liver aging. We integrated the multi-omics data of enrolled studies and reanalyzed them to identify key pathways and targets of liver aging. The results indicated that C-X-C motif chemokine ligand 9 (Cxcl9) was a regulator of liver aging. In addition, we provide a flowchart for liver aging research using multi-omics analysis and molecular experiments to help researchers conduct further research. Finally, we present emerging therapeutic treatments that prolong lifespan. In summary, using cells and animal models of liver aging, we can apply a multi-omics approach to find key metabolic pathways and target genes to mitigate the adverse effects of liver aging.

摘要

肝老化的研究已经变得突出,并引起了人们的极大兴趣,以揭示衰老的机制和治疗靶点,从而延长寿命。此外,多组学研究被广泛用于对肝老化进行进一步的机制研究。在这篇综述中,我们说明了肝脏老化过程中发生的变化,介绍了现有的肝老化模型,并强调了现有的肝老化多组学研究。我们整合了所纳入研究的多组学数据,并重新进行了分析,以确定肝老化的关键途径和靶点。结果表明,C-X-C 基序趋化因子配体 9(Cxcl9)是肝老化的调节因子。此外,我们还提供了一个使用多组学分析和分子实验进行肝老化研究的流程图,以帮助研究人员进行进一步的研究。最后,我们提出了新兴的延长寿命的治疗方法。总之,我们可以使用肝老化的细胞和动物模型,应用多组学方法来寻找关键的代谢途径和靶基因,以减轻肝老化的不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddf/10750291/ccd5a38fb272/ijbsv20p0280g001.jpg

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