circRNA basic information
circBase ID: -
Name: hsa_circ_ATP8B4
Synonym: circATP8B4
Host Gene: ATP8B4
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: extracellular vesicle
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0021042
MONDO name: glioma
Disease details: glioma
Disease DO ID:
-
Disease MeSH ID:
D005910
Disease NCIt ID:
C3059
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

U251 / U-251MG / RR-U251

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: miR-766-5p / miR-766
Biological function: May promote proliferation and radioresistance of normal glioma U251 cells; may serve as a potential biomarker for glioma radioresistance.
Molecular mechanism: circATP8B4 in RR-EVs may act as a miR-766-5p sponge; predicted circATP8B4-miR-766-5p-mRNA ceRNA mechanism may be involved in glioma radioresistance.
Biological pathway or process:

ceRNA regulation (other); proliferation (promotes); radioresistance (promotes); drug resistance (promotes)

Detected method:
Q
S
Validation methods:

RNA-seq; RT-qPCR; Back-Splice Junction PCR / divergent primers PCR; Bioinformatics Analysis; MTT

Clinical significance:

circATP8B4 from EVs could be a potential biomarker for glioma radioresistance.

Description:

circATP8B4 was up-regulated in extracellular vesicles derived from radioresistant U251 glioma cells compared with normal U251-derived EVs, and this expression change was validated by RT-qPCR. The study suggests that RR-EV-derived circATP8B4 may be transferred to recipient glioma cells and act as a miR-766-5p sponge in a predicted ceRNA mechanism, thereby promoting glioma cell radioresistance and potentially serving as a biomarker for glioma radioresistance.

Confidence score:

0.4851

Other information
Title:

Expression profiles and potential functions of circular RNAs in extracellular vesicles isolated from radioresistant glioma cells.

Journal: Oncology reports
Published: 2019
PubMed ID: 30664179
Study type:

combined biological and bioinformatics study

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