Research progress of lncRNA and miRNA in hepatic ischemia-reperfusion injury

小RNA 医学 生物信息学 再灌注损伤 长非编码RNA 非编码RNA 病态的 缺血 计算生物学 下调和上调 生物 基因 病理 遗传学 内科学
作者
Shan-Fei Zhu,Wei Yuan,Yongliang Du,Bai-Lin Wang
出处
期刊:Hepatobiliary & Pancreatic Diseases International [Elsevier BV]
卷期号:22 (1): 45-53 被引量:13
标识
DOI:10.1016/j.hbpd.2022.07.008
摘要

Hepatic ischemia-reperfusion injury (HIRI) is a common complication of liver surgeries, such as hepatectomy and liver transplantation. In recent years, several non-coding RNAs (ncRNAs) including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) have been identified as factors involved in the pathological progression of HIRI. In this review, we summarized the latest research on lncRNAs, miRNAs and the lncRNA-miRNA regulatory networks in HIRI. The PubMed and Web of Science databases were searched for articles published up to December 2021 using the following keywords: "hepatic ischemia-reperfusion injury", "lncRNA", "long non-coding RNA", "miRNA" and "microRNA". The bibliography of the selected articles was manually screened to identify additional studies. The mechanism of HIRI is complex, and involves multiple lncRNAs and miRNAs. The roles of lncRNAs such as AK139328, CCAT1, MALAT1, TUG1 and NEAT1 have been established in HIRI. In addition, numerous miRNAs are associated with apoptosis, autophagy, oxidative stress and cellular inflammation that accompany HIRI pathogenesis. Based on the literature, we conclude that four lncRNA-miRNA regulatory networks mediate the pathological progression of HIRI. Furthermore, the expression levels of some lncRNAs and miRNAs undergo significant changes during the progression of HIRI, and thus are potential prognostic markers and therapeutic targets. Complex lncRNA-miRNA-mRNA networks regulate HIRI progression through mutual activation and antagonism. It is necessary to screen for more HIRI-associated lncRNAs and miRNAs in order to identify novel therapeutic targets.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Uynaux完成签到,获得积分10
刚刚
匆匆发布了新的文献求助10
刚刚
pluto应助经竺采纳,获得10
刚刚
nini完成签到 ,获得积分10
刚刚
111发布了新的文献求助10
2秒前
小鹏发布了新的文献求助10
2秒前
2秒前
3秒前
无极微光应助春风采纳,获得20
3秒前
Carol完成签到,获得积分10
5秒前
JYH发布了新的文献求助10
5秒前
6秒前
研友_VZG7GZ应助无限的平露采纳,获得10
6秒前
6秒前
Orange应助科研通管家采纳,获得10
7秒前
Ava应助拓木幸子采纳,获得10
7秒前
7秒前
英姑应助科研通管家采纳,获得10
7秒前
今后应助科研通管家采纳,获得10
7秒前
赘婿应助科研通管家采纳,获得10
7秒前
7秒前
浮游应助科研通管家采纳,获得10
7秒前
99giddens应助科研通管家采纳,获得50
7秒前
7秒前
7秒前
Jasper应助daniel采纳,获得10
7秒前
干净的寒天完成签到,获得积分10
7秒前
7秒前
JamesPei应助科研通管家采纳,获得10
8秒前
8秒前
ding应助科研通管家采纳,获得10
8秒前
英姑应助科研通管家采纳,获得10
8秒前
Owen应助科研通管家采纳,获得10
8秒前
8秒前
8秒前
大个应助张泽辉采纳,获得10
8秒前
8秒前
8秒前
8秒前
8秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Applied Min-Max Approach to Missile Guidance and Control 3000
Metallurgy at high pressures and high temperatures 2000
Inorganic Chemistry Eighth Edition 1200
High Pressures-Temperatures Apparatus 1000
Free parameter models in liquid scintillation counting 1000
Standards for Molecular Testing for Red Cell, Platelet, and Neutrophil Antigens, 7th edition 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6319352
求助须知:如何正确求助?哪些是违规求助? 8135602
关于积分的说明 17055369
捐赠科研通 5373806
什么是DOI,文献DOI怎么找? 2852727
邀请新用户注册赠送积分活动 1830429
关于科研通互助平台的介绍 1682011