circRNA basic information
circBase ID: -
Name: hsa_circ_ARHGAP12
Synonym: -
Host Gene: ARHGAP12
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005311
MONDO name: atherosclerosis
Disease details: Atherosclerosis
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:

aortic tissues

Cell lines:

HUVECs

In vivo animal model:

genetically engineered animal model; other disease animal model

circRNA-disease information
Expression pattern:
UP
Associated gene: METTL14, HuR, ASPH mRNA
Associated microRNA: -
Biological function: circARHGAP12 promotes iron overload-induced lipid peroxidative damage, decreases cell viability, increases apoptosis, and facilitates atherosclerosis progression.
Molecular mechanism: METTL14-mediated m6A modification enhances circARHGAP12 stability and expression; circARHGAP12 binds HuR to stabilize ASPH mRNA and promote ASPH transcription.
Biological pathway or process:

m6A modification (other); mRNA stability (promotes); apoptosis (promotes); other pathway/process (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; RNase R Treatment; Actinomycin D / DRB Stability Assay; MeRIP / MeRIP-seq; RIP (RNA Immunoprecipitation); Transfection; CCK8; TUNEL; Western Blot; In Vivo Animal Model; Bioinformatics Analysis

Clinical significance:

-

Description:

circARHGAP12 is up-regulated in atherosclerotic tissues and ox-LDL-treated HUVECs. METTL14-mediated m6A modification increases circARHGAP12 stability, and circARHGAP12 binds HuR to stabilize ASPH mRNA, promoting ASPH transcription and aggravating iron overload-related lipid peroxidative damage, apoptosis, and AS progression.

Confidence score:

0.7394

Other information
Title:

Mechanisms of METTL14-Mediated m6A Modification in Promoting Iron Overload-Induced Lipid Peroxidative Damage in Vascular Endothelial Cells to Aggravate Atherosclerosis.

Journal: Journal of biochemical and molecular toxicology
Published: 2024
PubMed ID: 39588760
Study type:

biological research

Data availability: The data will be made available on request; Supporting Information S1: File
Code availability: -