circRNA basic information
circBase ID: hsa_circ_0005105
Name: hsa_circ_SEC24A
Synonym: circSEC24A
Host Gene: -
Genomic location(hg19): chr5:134022479-134023989:+
Genomic location(hg38): chr5:134686789-134688299:+
Subcellular localization: not tested
 
 
 
 
 
 
 
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:

OA cartilage tissues; normal cartilage tissues

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SOX5, TNF-alpha, IL-6
Associated microRNA: miR-142-5p
Biological function: Promotes IL-1beta-induced chondrocyte injury by decreasing cell proliferation and increasing apoptosis and inflammation.
Molecular mechanism: circSEC24A acts as a molecular sponge of miR-142-5p to regulate SOX5 expression in chondrocytes.
Biological pathway or process:

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

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; MTT; Colony Formation Assay; Annexin V/PI Flow Cytometry; Western Blot; Luciferase Reporter Assay; RIP (RNA Immunoprecipitation); Bioinformatics Analysis

Clinical significance:

providing a promising target for gene therapy

Description:

circSEC24A is up-regulated in OA cartilage tissues, OA chondrocytes, and IL-1beta-treated chondrocytes. It aggravates OA-like chondrocyte injury by inhibiting proliferation and promoting apoptosis and inflammatory factor expression, acting through a circSEC24A/miR-142-5p/SOX5 ceRNA axis.

Confidence score:

0.7032

Other information
Title:

CircSEC24A promotes IL-1beta-induced apoptosis and inflammation in chondrocytes by regulating miR-142-5p/SOX5 axis.

Journal: Biotechnology and applied biochemistry
Published: 2022
PubMed ID: 33751650
Study type:

combined biological and clinical study

Data availability: available from the corresponding author on reasonable request
Code availability: -