亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

A Circular RNA, Cholangiocarcinoma‐Associated Circular RNA 1, Contributes to Cholangiocarcinoma Progression, Induces Angiogenesis, and Disrupts Vascular Endothelial Barriers

环状RNA 癌症研究 核糖核酸 血管生成 生物 医学 内科学 基因 遗传学
作者
Yi Xu,Kaiming Leng,Yue Yao,Pengcheng Kang,Guanqun Liao,Yi Han,Guangjun Shi,Daolin Ji,Peng Huang,Wangyang Zheng,Zhenglong Li,Jinglin Li,Lining Huang,Liang Yu,Yongxu Zhou,Xingming Jiang,Hao Wang,Chunlong Li,Zhilei Su,Sheng Tai
出处
期刊:Hepatology [Wiley]
卷期号:73 (4): 1419-1435 被引量:149
标识
DOI:10.1002/hep.31493
摘要

Circular RNAs (circRNAs) and extracellular vesicles (EVs) are involved in various malignancies. We aimed to clarify the functions and mechanisms of dysregulated circRNAs in the cells and EVs of cholangiocarcinoma (CCA).CircRNA microarray was used to identify circRNA expression profiles in CCA tissues and bile-derived EVs (BEVs). CCA-associated circRNA 1 (circ-CCAC1) expression was measured by quantitative real-time PCR. The clinical importance of circ-CCAC1 was analyzed by receiver operating characteristic curves, Fisher's exact test, Kaplan-Meier plots, and Cox regression model. The functions of circ-CCAC1 and exosomal circ-CCAC1 were explored in CCA cells and human umbilical vein endothelial cells (HUVECs), respectively. Different animal models were used to verify the in vitro results. RNA sequencing, bioinformatics, RNA immunoprecipitation, RNA pulldown, chromatin immunoprecipitation followed by sequencing, and luciferase reporter assays were used to determine the regulatory networks of circ-CCAC1 in CCA cells and HUVECs. Circ-CCAC1 levels were increased in cancerous bile-resident EVs and tissues. The diagnostic and prognostic values of circ-CCAC1 were identified in patients with CCA. For CCA cells, circ-CCAC1 increased cell progression by sponging miR-514a-5p to up-regulate Yin Yang 1 (YY1). Meanwhile, YY1 directly bound to the promoter of calcium modulating ligand to activate its transcription. Moreover, circ-CCAC1 from CCA-derived EVs was transferred to endothelial monolayer cells, disrupting endothelial barrier integrity and inducing angiogenesis. Mechanistically, circ-CCAC1 increased cell leakiness by sequestering enhancer of zeste homolog 2 in the cytoplasm, thus elevating SH3 domain-containing GRB2-like protein 2 expression to reduce the levels of intercellular junction proteins. In vivo studies further showed that increased circ-CCAC1 levels in circulating EVs and cells accelerated both CCA tumorigenesis and metastasis.Circ-CCAC1 plays a vital role in CCA tumorigenesis and metastasis and may be an important biomarker/therapeutic target for CCA.
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
大模型应助Shrine采纳,获得10
8秒前
15秒前
复杂冬灵完成签到,获得积分10
16秒前
18秒前
ren发布了新的文献求助10
21秒前
桃桃发布了新的文献求助10
21秒前
25秒前
汉堡包应助科研通管家采纳,获得10
26秒前
酷波er应助科研通管家采纳,获得10
26秒前
26秒前
null应助科研通管家采纳,获得30
26秒前
null应助科研通管家采纳,获得30
26秒前
26秒前
Hello应助科研通管家采纳,获得30
26秒前
桃桃完成签到,获得积分10
28秒前
37秒前
40秒前
Shrine发布了新的文献求助10
48秒前
啦啦啦发布了新的文献求助10
51秒前
1分钟前
顾卿莀发布了新的文献求助30
1分钟前
1分钟前
纯真听寒完成签到 ,获得积分10
1分钟前
小兔子乖乖完成签到 ,获得积分10
1分钟前
汉堡包应助schaffner采纳,获得10
1分钟前
1分钟前
顾卿莀完成签到,获得积分20
1分钟前
1分钟前
彭于晏应助马上毕业采纳,获得10
1分钟前
Tjh发布了新的文献求助10
1分钟前
1分钟前
1分钟前
Lily完成签到,获得积分10
1分钟前
fabius0351完成签到,获得积分10
1分钟前
副反应发布了新的文献求助10
1分钟前
1分钟前
Tjh完成签到,获得积分10
1分钟前
马上毕业发布了新的文献求助10
1分钟前
Wone3完成签到 ,获得积分10
1分钟前
低调000完成签到,获得积分10
2分钟前
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
Kinesiophobia : a new view of chronic pain behavior 3000
Les Mantodea de guyane 2500
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
Brittle Fracture in Welded Ships 500
Lloyd's Register of Shipping's Approach to the Control of Incidents of Brittle Fracture in Ship Structures 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5942509
求助须知:如何正确求助?哪些是违规求助? 7072291
关于积分的说明 15888720
捐赠科研通 5073178
什么是DOI,文献DOI怎么找? 2728900
邀请新用户注册赠送积分活动 1687664
关于科研通互助平台的介绍 1613513