circRNA basic information
circBase ID: hsa_circ_0005752
Name: hsa_circ_LPAR1
Synonym: -
Host Gene: LPAR1
Genomic location(hg19): chr9:113771427-113773970:-
Genomic location(hg38): chr9:111009147-111011690:-
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005298
MONDO name: osteoporosis
Disease details: osteoporosis
Disease DO ID:
11476
Disease MeSH ID:
D010024
Disease NCIt ID:
C3298
Disease ICD11 ID:
2113001430
Disease OMIM ID:
166710
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

ADSCs

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: MDM2, p53, RUNX3, LPAR1
Associated microRNA: miR-496
Biological function: Promotes osteogenic differentiation of ADSCs; increases osteogenic markers (Runx2, ALP, Osx, OCN) and decreases p53.
Molecular mechanism: Acts as a ceRNA by sponging miR-496 to relieve repression of MDM2, thereby inhibiting p53 and promoting osteogenic differentiation; RUNX3 binds the LPAR1 promoter to increase hsa_circ_0005752 expression.
Biological pathway or process:

ceRNA regulation (promotes); p53 signaling (inhibits); proliferation (other)

Detected method:
Q
Validation methods:

RT-qPCR; RNA Pull-Down; RIP (RNA Immunoprecipitation); Luciferase Reporter Assay; Transfection; Western Blot; In Vivo Animal Model

Clinical significance:

Provided a new therapeutic strategy for osteoporosis.

Description:

In OM-induced ADSC osteogenesis (osteoporosis-relevant context), hsa_circ_0005752 is up-regulated and promotes osteogenic differentiation. It functions as a ceRNA that sponges miR-496 to increase MDM2 and suppress p53, and its expression is transcriptionally enhanced by RUNX3 via the LPAR1 promoter.

Confidence score:

0.6145

Other information
Title:

RUNX3 derived hsa_circ_0005752 accelerates the osteogenic differentiation of adipose-derived stem cells via the miR-496/MDM2-p53 pathway.

Journal: Regenerative therapy
Published: 2021
PubMed ID: 34754888
Study type:

biological research

Data availability: All data collected and analyzed during the current study are available from the corresponding author on reasonable request.
Code availability: -