circRNA basic information
circBase ID: -
Name: hsa_circ_PRDM5
Synonym: circ-PRDM5
Host Gene: PRDM5
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005129
MONDO name: cataract
Disease details: posterior capsule opacities
Disease DO ID:
83
Disease MeSH ID:
D002386
Disease NCIt ID:
C26713
Disease ICD11 ID:
109841337
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

PCO tissues; normal posterior capsular tissues

Cell lines:

SRA01/04; LECs

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: COL1A2, Ago2
Associated microRNA: miR-92b-3p
Biological function: TGF-beta2-induced circ-PRDM5 promotes LEC viability, migration, invasion, and EMT in PCO models; circ-PRDM5 knockdown reduces TGF-beta2-induced migration, invasion, and EMT.
Molecular mechanism: circ-PRDM5 acts as a ceRNA by sponging miR-92b-3p, thereby increasing COL1A2 expression and promoting TGF-beta2-induced migration, invasion, and EMT in LECs.
Biological pathway or process:

ceRNA regulation (promotes); migration (promotes); invasion (promotes); EMT (promotes); proliferation (promotes)

Detected method:
Q
Validation methods:

RNase R Treatment; RT-qPCR; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); Luciferase Reporter Assay; Transfection; MTT; Transwell Assay; Wound Healing Assay; Western Blot; Bioinformatics Analysis

Clinical significance:

circ-PRDM5 might be a potential therapeutic target for PCO.

Description:

circ-PRDM5 is up-regulated in PCO tissues and TGF-beta2-stimulated human lens epithelial cells. It promotes LEC viability, migration, invasion, and EMT by acting as a miR-92b-3p sponge to increase COL1A2 expression, suggesting a potential therapeutic role in PCO.

Confidence score:

0.7785

Other information
Title:

TGF-beta2-induced circ-PRDM5 regulates migration, invasion, and EMT through the miR-92b-3p/COL1A2 pathway in human lens epithelial cells.

Journal: Journal of molecular histology
Published: 2022
PubMed ID: 35083632
Study type:

combined biological and clinical study

Data availability: Supplementary material available at https:// doi. org/ 10. 1007/ s10735-021-10053-7
Code availability: -