• 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

p53在肝纤维化中的作用。

The role of p53 in liver fibrosis.

作者信息

Yu Siyu, Ji Guang, Zhang Li

机构信息

Institute of Digestive Diseases, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Pharmacol. 2022 Oct 24;13:1057829. doi: 10.3389/fphar.2022.1057829. eCollection 2022.

DOI:10.3389/fphar.2022.1057829
PMID:36353498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9637836/
Abstract

The tumor suppressor p53 is the central hub of a molecular network, which controls cell proliferation and death, and also plays an important role in the occurrence and development of liver fibrosis. The abundant post-translational processing and modification endow the functional diversity of p53. Considering the relationship between p53 and liver fibrosis, drug intervention targeting p53 or management of p53 regulation might be effective strategies to treat liver fibrosis. Here, we systematically discuss the regulation of p53 in different liver cells (hepatocytes, immune cells, HSCs, ) and the role of p53 in the development of liver fibrosis, and propose possible interventions to prevent the pathogenic processes of liver fibrosis.

摘要

肿瘤抑制因子p53是一个分子网络的核心枢纽,该网络控制细胞增殖和死亡,并且在肝纤维化的发生和发展中也起着重要作用。丰富的翻译后加工和修饰赋予了p53功能多样性。考虑到p53与肝纤维化之间的关系,针对p53的药物干预或对p53调控的管理可能是治疗肝纤维化的有效策略。在此,我们系统地讨论了p53在不同肝细胞(肝细胞、免疫细胞、肝星状细胞)中的调控以及p53在肝纤维化发展中的作用,并提出了预防肝纤维化致病过程的可能干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ca/9637836/96967daa273e/fphar-13-1057829-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ca/9637836/e9be3fb5fe3a/fphar-13-1057829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ca/9637836/96967daa273e/fphar-13-1057829-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ca/9637836/e9be3fb5fe3a/fphar-13-1057829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ca/9637836/96967daa273e/fphar-13-1057829-g002.jpg

相似文献

1
The role of p53 in liver fibrosis.p53在肝纤维化中的作用。
Front Pharmacol. 2022 Oct 24;13:1057829. doi: 10.3389/fphar.2022.1057829. eCollection 2022.
2
P53-dependent induction of ferroptosis is required for artemether to alleviate carbon tetrachloride-induced liver fibrosis and hepatic stellate cell activation.青蒿素依赖 P53 诱导的铁死亡对减轻四氯化碳诱导的肝纤维化和肝星状细胞激活是必需的。
IUBMB Life. 2019 Jan;71(1):45-56. doi: 10.1002/iub.1895. Epub 2018 Oct 15.
3
Activation of the miR-34a/SIRT1/p53 Signaling Pathway Contributes to the Progress of Liver Fibrosis via Inducing Apoptosis in Hepatocytes but Not in HSCs.miR-34a/SIRT1/p53信号通路的激活通过诱导肝细胞而非肝星状细胞凋亡促进肝纤维化进展。
PLoS One. 2016 Jul 7;11(7):e0158657. doi: 10.1371/journal.pone.0158657. eCollection 2016.
4
Interleukin-10 induces senescence of activated hepatic stellate cells via STAT3-p53 pathway to attenuate liver fibrosis.白细胞介素-10 通过 STAT3-p53 通路诱导活化的肝星状细胞衰老,从而减轻肝纤维化。
Cell Signal. 2020 Feb;66:109445. doi: 10.1016/j.cellsig.2019.109445. Epub 2019 Nov 12.
5
Effects of recombinant human adenovirus-p53 on the regression of hepatic fibrosis.重组人腺病毒-p53对肝纤维化消退的影响。
Int J Mol Med. 2016 Oct;38(4):1093-100. doi: 10.3892/ijmm.2016.2716. Epub 2016 Aug 26.
6
MicroRNA-145 induces the senescence of activated hepatic stellate cells through the activation of p53 pathway by ZEB2.MicroRNA-145 通过 ZEB2 激活 p53 通路诱导活化的肝星状细胞衰老。
J Cell Physiol. 2019 May;234(5):7587-7599. doi: 10.1002/jcp.27521. Epub 2018 Nov 27.
7
mA methylation is required for dihydroartemisinin to alleviate liver fibrosis by inducing ferroptosis in hepatic stellate cells.二氢青蒿素通过诱导肝星状细胞发生铁死亡来减轻肝纤维化,这需要 mA 甲基化。
Free Radic Biol Med. 2022 Mar;182:246-259. doi: 10.1016/j.freeradbiomed.2022.02.028. Epub 2022 Mar 4.
8
Soluble egg antigens of Schistosoma japonicum induce senescence in activated hepatic stellate cells by activation of the STAT3/p53/p21 pathway.日本血吸虫可溶性虫卵抗原通过激活STAT3/p53/p21信号通路诱导活化的肝星状细胞衰老。
Sci Rep. 2016 Aug 4;6:30957. doi: 10.1038/srep30957.
9
The BRD7-P53-SLC25A28 axis regulates ferroptosis in hepatic stellate cells.BRD7-P53-SLC25A28 轴调控肝星状细胞中的铁死亡。
Redox Biol. 2020 Sep;36:101619. doi: 10.1016/j.redox.2020.101619. Epub 2020 Jun 24.
10
TRIM26 Induces Ferroptosis to Inhibit Hepatic Stellate Cell Activation and Mitigate Liver Fibrosis Through Mediating SLC7A11 Ubiquitination.TRIM26通过介导SLC7A11泛素化诱导铁死亡以抑制肝星状细胞激活并减轻肝纤维化
Front Cell Dev Biol. 2021 Mar 25;9:644901. doi: 10.3389/fcell.2021.644901. eCollection 2021.

引用本文的文献

1
Inhibiting CXCR6 promotes senescence of activated hepatic stellate cells with limited proinflammatory SASP to attenuate hepatic fibrosis.抑制CXCR6可促进活化肝星状细胞衰老,同时减少促炎衰老相关分泌表型,从而减轻肝纤维化。
Open Life Sci. 2025 Aug 8;20(1):20251151. doi: 10.1515/biol-2025-1151. eCollection 2025.
2
Calorie-restriction treatment mitigates the aging in rat liver model.热量限制疗法可减轻大鼠肝脏模型中的衰老。
Biogerontology. 2025 May 7;26(3):108. doi: 10.1007/s10522-025-10245-8.
3
Discovery of Genomic Targets and Therapeutic Candidates for Liver Cancer Using Single-Cell RNA Sequencing and Molecular Docking.

本文引用的文献

1
FOSL2 deficiency delays nonalcoholic steatohepatitis progression by regulating LY6D-mediated NLRP3 activation.FOSL2 缺乏通过调节 LY6D 介导的 NLRP3 激活来延缓非酒精性脂肪性肝炎的进展。
Hum Cell. 2022 Nov;35(6):1752-1765. doi: 10.1007/s13577-022-00760-y. Epub 2022 Aug 5.
2
Cardiomyocyte-specific knockout of ADAM17 ameliorates left ventricular remodeling and function in diabetic cardiomyopathy of mice.心肌细胞特异性敲除 ADAM17 可改善糖尿病心肌病小鼠的左心室重构和功能。
Signal Transduct Target Ther. 2022 Aug 1;7(1):259. doi: 10.1038/s41392-022-01054-3.
3
Cellular Mechanisms of Liver Fibrosis.
利用单细胞RNA测序和分子对接技术发现肝癌的基因组靶点和治疗候选物
Biology (Basel). 2025 Apr 17;14(4):431. doi: 10.3390/biology14040431.
4
A Novel Mechanism of the p53 Isoform Δ40p53α in Regulating Collagen III Expression in TGFβ1-Induced LX-2 Human Hepatic Stellate Cells.p53亚型Δ40p53α在调节转化生长因子β1诱导的LX-2人肝星状细胞中Ⅲ型胶原蛋白表达的新机制
FASEB J. 2025 Apr 30;39(8):e70541. doi: 10.1096/fj.202403146RR.
5
Insulin receptor responsiveness governs TGFβ-induced hepatic stellate cell activation: Insulin resistance instigates liver fibrosis.胰岛素受体反应性调控转化生长因子β诱导的肝星状细胞活化:胰岛素抵抗引发肝纤维化。
FASEB J. 2025 Mar 15;39(5):e70427. doi: 10.1096/fj.202402169R.
6
Characterization of liver, adipose, and fecal microbiome in obese patients with MASLD: links with disease severity and metabolic dysfunction parameters.伴有代谢功能障碍相关脂肪性肝病的肥胖患者肝脏、脂肪组织及粪便微生物群的特征:与疾病严重程度及代谢功能障碍参数的关联
Microbiome. 2025 Jan 14;13(1):9. doi: 10.1186/s40168-024-02004-7.
7
Magnoflorine ameliorates hepatic fibrosis and hepatic stellate cell activation by regulating ferroptosis signaling pathway.木兰碱通过调节铁死亡信号通路改善肝纤维化和肝星状细胞激活。
Heliyon. 2024 Nov 8;10(22):e39892. doi: 10.1016/j.heliyon.2024.e39892. eCollection 2024 Nov 30.
8
Oral N-acetylcysteine ameliorates liver fibrosis and enhances regenerative responses in Mdr2 knockout mice.口服 N-乙酰半胱氨酸可改善 Mdr2 敲除小鼠的肝纤维化并增强其再生反应。
Sci Rep. 2024 Nov 3;14(1):26513. doi: 10.1038/s41598-024-78387-2.
9
GBT1118, a Voxelotor Analog, Ameliorates Hepatopathy in Sickle Cell Disease.GBT1118,一种伏洛托拉肖类似物,可改善镰状细胞病中的肝病。
Medicina (Kaunas). 2024 Sep 26;60(10):1581. doi: 10.3390/medicina60101581.
10
Probing Liver Injuries Induced by Thioacetamide in Human In Vitro Pooled Hepatocyte Experiments.探讨硫代乙酰胺在人离体混合肝细胞实验中诱导的肝损伤。
Int J Mol Sci. 2024 Mar 13;25(6):3265. doi: 10.3390/ijms25063265.
肝纤维化的细胞机制
Front Pharmacol. 2021 May 6;12:671640. doi: 10.3389/fphar.2021.671640. eCollection 2021.
4
p53: A Key Protein That Regulates Pulmonary Fibrosis.p53:一种调节肺纤维化的关键蛋白。
Oxid Med Cell Longev. 2020 Nov 29;2020:6635794. doi: 10.1155/2020/6635794. eCollection 2020.
5
Short-term exposure to ambient particulate matter and outpatient visits for respiratory diseases among children: A time-series study in five Chinese cities.短期暴露于环境细颗粒物与儿童呼吸道疾病门诊就诊率之间的关系:中国五个城市的时间序列研究。
Chemosphere. 2021 Jan;263:128214. doi: 10.1016/j.chemosphere.2020.128214. Epub 2020 Sep 8.
6
Efficacy and safety of anti-hepatic fibrosis drugs.抗肝纤维化药物的疗效与安全性。
World J Gastroenterol. 2020 Nov 7;26(41):6304-6321. doi: 10.3748/wjg.v26.i41.6304.
7
Loss of hepatocyte cell division leads to liver inflammation and fibrosis.肝细胞分裂丧失可导致肝脏炎症和纤维化。
PLoS Genet. 2020 Nov 4;16(11):e1009084. doi: 10.1371/journal.pgen.1009084. eCollection 2020 Nov.
8
Silencing p53 inhibits interleukin 10-induced activated hepatic stellate cell senescence and fibrotic degradation in vivo.沉默 p53 抑制白细胞介素 10 诱导的活化的肝星状细胞衰老和体内纤维化降解。
Exp Biol Med (Maywood). 2021 Feb;246(4):447-458. doi: 10.1177/1535370220960391. Epub 2020 Oct 7.
9
The BRD7-P53-SLC25A28 axis regulates ferroptosis in hepatic stellate cells.BRD7-P53-SLC25A28 轴调控肝星状细胞中的铁死亡。
Redox Biol. 2020 Sep;36:101619. doi: 10.1016/j.redox.2020.101619. Epub 2020 Jun 24.
10
miR-34a promotes liver fibrosis in patients with chronic hepatitis via mediating Sirt1/p53 signaling pathway.miR-34a 通过介导 Sirt1/p53 信号通路促进慢性肝炎患者肝纤维化。
Pathol Res Pract. 2020 May;216(5):152876. doi: 10.1016/j.prp.2020.152876. Epub 2020 Feb 13.