circRNA basic information
circBase ID: -
Name: hsa_circ_STK39
Synonym: circSTK39
Host Gene: STK39
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0004847
MONDO name: senile cataract
Disease details: age-related cataract
Disease DO ID:
9669
Disease MeSH ID:
-
Disease NCIt ID:
C35012
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

anterior lens capsules; lens tissues

Cell lines:

SRA01/04

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DN
Associated gene: ERCC6
Associated microRNA: miR-125a-5p
Biological function: Protects against H2O2-induced human lens epithelial cell injury by promoting cell viability and proliferation and inhibiting apoptosis and oxidative stress.
Molecular mechanism: circSTK39 acts as a miR-125a-5p sponge and regulates ERCC6 expression through the miR-125a-5p/ERCC6 pathway.
Biological pathway or process:

proliferation (promotes); apoptosis (inhibits); ceRNA regulation (other); other pathway/process (inhibits)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Nuclear-Cytoplasmic Fractionation; Transfection; CCK8; EdU Staining; Annexin V/PI Flow Cytometry; Western Blot; Luciferase Reporter Assay; RIP (RNA Immunoprecipitation); RNA Pull-Down; Bioinformatics Analysis

Clinical significance:

Potential therapeutic relevance for ARC therapy.

Description:

circSTK39 is downregulated in ARC lens tissues and H2O2-induced SRA01/04 cells. Its overexpression protects human lens epithelial cells from H2O2-induced injury by promoting proliferation and inhibiting apoptosis and oxidative stress, acting through a circSTK39/miR-125a-5p/ERCC6 ceRNA axis.

Confidence score:

0.7507

Other information
Title:

Ectopic circSTK39 Expression Ameliorates Hydrogen Peroxide-Induced Human Lens Epithelial Cell Apoptosis and Oxidative Stress through the miR-125a-5p/ERCC6 Pathway.

Journal: Current eye research
Published: 2023
PubMed ID: 36322706
Study type:

combined biological and clinical study

Data availability: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Code availability: -