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 [Lippincott Williams & Wilkins]
卷期号:73 (4): 1419-1435 被引量:141
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
vvv发布了新的文献求助50
刚刚
圈圈发布了新的文献求助10
1秒前
recovery完成签到,获得积分10
2秒前
小马完成签到,获得积分10
2秒前
hakunamatata完成签到 ,获得积分10
3秒前
小长夜完成签到,获得积分10
3秒前
3秒前
cunzhang发布了新的文献求助10
5秒前
zz完成签到,获得积分10
5秒前
5秒前
5秒前
5秒前
JamesPei应助WINK采纳,获得10
6秒前
李健的小迷弟应助lanmin采纳,获得10
6秒前
传统的复天完成签到,获得积分10
6秒前
8秒前
9秒前
自然完成签到,获得积分10
9秒前
SHAO应助WMX采纳,获得10
9秒前
9秒前
友人z关注了科研通微信公众号
9秒前
大牛发布了新的文献求助10
10秒前
共享精神应助鲜艳的烧鹅采纳,获得10
10秒前
Ivy完成签到,获得积分20
11秒前
11秒前
一品真意完成签到,获得积分10
13秒前
zXX发布了新的文献求助10
13秒前
14秒前
14秒前
15秒前
15秒前
vvv完成签到,获得积分10
16秒前
16秒前
16秒前
寒冷的如南完成签到,获得积分10
17秒前
17秒前
WINK发布了新的文献求助10
18秒前
lanmin发布了新的文献求助10
19秒前
博修发布了新的文献求助10
19秒前
20秒前
高分求助中
The Mother of All Tableaux Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 1370
生物降解型栓塞微球市场(按产品类型、应用和最终用户)- 2030 年全球预测 1000
Statistical Analysis of fMRI Data, second edition (Mit Press) 2nd ed 500
Lidocaine regional block in the treatment of acute gouty arthritis of the foot 400
Ecological and Human Health Impacts of Contaminated Food and Environments 400
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 360
International Relations at LSE: A History of 75 Years 308
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3933697
求助须知:如何正确求助?哪些是违规求助? 3478788
关于积分的说明 11003021
捐赠科研通 3208795
什么是DOI,文献DOI怎么找? 1773300
邀请新用户注册赠送积分活动 860287
科研通“疑难数据库(出版商)”最低求助积分说明 797626