circRNA basic information
circBase ID: -
Name: hsa_circ_CDR1AS
Synonym: CDR1as
Host Gene: CDR1as
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005178
MONDO name: osteoarthritis
Disease details: osteoarthritis
Disease DO ID:
8398
Disease MeSH ID:
D010003
Disease NCIt ID:
C3293
Disease ICD11 ID:
558562409
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

knee joint cartilage / articular cartilage

Cell lines:

HEK-293 T

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: FGF-2, MEK/ERK signaling pathway
Associated microRNA: miR-641
Biological function: Promotes osteoarthritis progression by promoting extracellular matrix catabolism and inflammation (increases MMP13 and IL-6, decreases Col II).
Molecular mechanism: Acts as a miRNA sponge (ceRNA-like) for miR-641, thereby regulating FGF-2 and activating MEK/ERK signaling to modulate ECM metabolism and inflammation.
Biological pathway or process:

ERK (promotes); inflammation (promotes); other pathway/process (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; RNA Pull-Down; Luciferase Reporter Assay; Western Blot; IF (Immunofluorescence); Bioinformatics Analysis

Clinical significance:

Could be utilized as a biomarker and target for OA therapy.

Description:

circRNA-CDR1as is up-regulated in OA chondrocytes and promotes OA progression. It sponges miR-641, derepressing FGF-2 and activating MEK/ERK signaling, which increases MMP13 and IL-6 and reduces type II collagen, thereby enhancing ECM catabolism and inflammation.

Confidence score:

0.6903

Other information
Title:

Circular RNA-CDR1as acts as the sponge of microRNA-641 to promote osteoarthritis progression.

Journal: Journal of inflammation (London, England)
Published: 2020
PubMed ID: 32099534
Study type:

combined biological and clinical study

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