circRNA basic information
circBase ID: -
Name: hsa_circ_PTPRA
Synonym: circRNA-PTPRA
Host Gene: PTPRA
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:

serum

Cell lines:

HUVECs; HEK293T

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: miR-671-5p
Biological function: circRNA-PTPRA knockdown protects against ox-LDL-induced HUVEC injury by increasing cell viability, reducing apoptosis, and suppressing inflammatory cytokine secretion.
Molecular mechanism: circRNA-PTPRA functions as a sponge for miR-671-5p; circRNA-PTPRA downregulation upregulates miR-671-5p to repress ox-LDL-induced endothelial cell injury.
Biological pathway or process:

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

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Bioinformatics Analysis; Luciferase Reporter Assay; RNA Pull-Down; Transfection; CCK8; Annexin V/PI Flow Cytometry; ELISA; Western Blot

Clinical significance:

circRNA-PTPRA is upregulated in the serum of patients with AS and may provide early screening molecules and potential therapeutic targets for AS.

Description:

circRNA-PTPRA is upregulated in the serum of AS patients and in ox-LDL-treated HUVECs. It promotes ox-LDL-induced endothelial cell injury by sponging miR-671-5p, while circRNA-PTPRA knockdown restores miR-671-5p, improves cell viability, reduces apoptosis, and suppresses inflammatory cytokine secretion.

Confidence score:

0.7032

Other information
Title:

CircRNA-PTPRA Knockdown Inhibits Atherosclerosis Progression by Repressing ox-LDL-Induced Endothelial Cell Injury via Sponging of miR-671-5p.

Journal: Biochemical genetics
Published: 2023
PubMed ID: 35817886
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: -