The role and regulation of SIRT1 in pulmonary fibrosis

被引:1
|
作者
Ma, Xinyi [1 ]
Jiang, Mengna [1 ]
Ji, Wenqian [2 ]
Yu, Mengjiao [1 ]
Tang, Can [1 ]
Tian, Kai [1 ]
Gao, Zhengnan [1 ]
Su, Liling [3 ]
Tang, Juan [1 ]
Zhao, Xinyuan [1 ]
机构
[1] Nantong Univ, Sch Publ Hlth, Dept Occupat Med & Environm Toxicol, Nantong Key Lab Environm Toxicol, Nantong 226019, Peoples R China
[2] Southwest Univ, Coll Int Studies, Chongqing, Peoples R China
[3] Jiangxi Med Coll, Dept Clin Med, Shangrao 334000, Peoples R China
基金
中国国家自然科学基金;
关键词
Pulmonary fibrosis; SIRT1; Lung aging; Autophagy; Apoptosis`; RESVERATROL; SENESCENCE; ACTIVATORS; EMPHYSEMA; THERAPY; CANCER; LUNGS;
D O I
10.1007/s11033-024-09296-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pulmonary fibrosis (PF) is a progressive and fatal lung disease with high incidence and a lack of effective treatment, which is a severe public health problem. PF has caused a huge socio-economic burden, and its pathogenesis has become a research hotspot. SIRT1 is a nicotinamide adenosine dinucleotide (NAD)-dependent sirtuin essential in tumours, Epithelial mesenchymal transition (EMT), and anti-aging. Numerous studies have demonstrated after extensive research that it is crucial in preventing the progression of pulmonary fibrosis. This article reviews the biological roles and mechanisms of SIRT1 in regulating the progression of pulmonary fibrosis in terms of EMT, oxidative stress, inflammation, aging, autophagy, and discusses the potential of SIRT1 as a therapeutic target for pulmonary fibrosis, and provides a new perspective on therapeutic drugs and prognosis prospects.
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收藏
页数:12
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