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:
0005311
MONDO name: atherosclerosis
Disease details: vascular calcification
Disease DO ID:
1936
Disease MeSH ID:
D050197
Disease NCIt ID:
C35768
Disease ICD11 ID:
109367356
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

serum

Cell lines:

VSMCs

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DN
Associated gene: FUS, SIRT1
Associated microRNA: -
Biological function: Inhibits vascular smooth muscle cell calcification and calcium deposition.
Molecular mechanism: circHIPK3 binds/recruits the RNA-binding protein FUS to stabilize SIRT1 mRNA, activating SIRT1/PGC-1alpha signaling and promoting MFN2 expression to alleviate VSMC calcification.
Biological pathway or process:

other pathway/process (inhibits); vascular calcification (inhibits); mRNA stability (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; RIP (RNA Immunoprecipitation); RNA Pull-Down; Actinomycin D / DRB Stability Assay; Transfection; Western Blot; ELISA

Clinical significance:

circHIPK3 is down-regulated in AS serum and may be a potential therapeutic target for vascular calcification.

Description:

circHIPK3 is down-regulated in AS serum and in a beta-GP-induced VSMC calcification model. Its overexpression inhibits ALP activity and calcium deposition by recruiting FUS to stabilize SIRT1 mRNA and activating the SIRT1/PGC-1alpha/MFN2 pathway, thereby alleviating vascular calcification.

Confidence score:

0.6575

Other information
Title:

CircHIPK3 relieves vascular calcification via mediating SIRT1/PGC-1alpha/MFN2 pathway by interacting with FUS.

Journal: BMC cardiovascular disorders
Published: 2023
PubMed ID: 38012555
Study type:

combined biological and clinical study

Data availability: The datasets used or analyzed during the current study are available from the corresponding author on reasonable request.
Code availability: -