circRNA basic information
circBase ID: -
Name: hsa_circ_HIPK3
Synonym: circHIPK3
Host Gene: HIPK3
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005203
MONDO name: ischemia reperfusion injury
Disease details: myocardial ischemia/reperfusion injury
Disease DO ID:
-
Disease MeSH ID:
D015427
Disease NCIt ID:
-
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

HCM

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: Bax, Bcl-2
Associated microRNA: miRNA-124-3p, miR-124-3p
Biological function: CircHIPK3 aggravates myocardial I/R injury, inhibits proliferative ability, and induces apoptosis of cardiomyocytes.
Molecular mechanism: CircHIPK3 binds to miRNA-124-3p and negatively regulates miRNA-124-3p; circHIPK3 overexpression upregulates Bax and downregulates Bcl-2, promoting cardiomyocyte apoptosis.
Biological pathway or process:

apoptosis (promotes); proliferation (inhibits); ceRNA regulation (other)

Detected method:
Q
Validation methods:

RT-qPCR; Bioinformatics Analysis; Luciferase Reporter Assay; Transfection; CCK8; Annexin V/PI Flow Cytometry; Western Blot

Clinical significance:

CircHIPK3 may serve as a potential therapeutic target for I/R injury.

Description:

This study found that circHIPK3 is up-regulated in an in vitro HCM cell model of myocardial I/R injury. CircHIPK3 aggravates myocardial I/R injury by binding to and inhibiting miRNA-124-3p, thereby suppressing cardiomyocyte proliferation and promoting apoptosis with altered Bax and Bcl-2 expression. The authors propose circHIPK3 as a potential therapeutic target for I/R injury.

Confidence score:

0.5554

Other information
Title:

CircHIPK3 aggravates myocardial ischemia-reperfusion injury by binding to miRNA-124-3p.

Journal: European review for medical and pharmacological sciences
Published: 2019
PubMed ID: 31799682
Study type:

biological research

Data availability: -
Code availability: -