circRNA basic information
circBase ID: -
Name: mmu_circ_ZNF609
Synonym: circZNF609
Host Gene: ZNF609
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0100313
MONDO name: focal segmental glomerulosclerosis
Disease details: focal segmental glomerulosclerosis
Disease DO ID:
1312
Disease MeSH ID:
D005923
Disease NCIt ID:
C37308
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Mouse
Species details: Mus musculus
Tissue specimen:

renal biopsies; kidney tissue; kidney tissues; glomeruli; tubules

Cell lines:

HK-2

In vivo animal model:

other disease animal model

circRNA-disease information
Expression pattern:
UP
Associated gene: COL1 mRNA, COL1
Associated microRNA: miR-615-5p
Biological function: circZNF609 is involved in FSGS pathogenesis, positively correlates with podocyte injury and renal fibrosis, and may promote COL1 overproduction by sponging miR-615-5p.
Molecular mechanism: ceRNA mechanism: circZNF609 may sponge miR-615-5p, thereby increasing COL1 production and contributing to renal fibrosis and podocyte injury in FSGS.
Biological pathway or process:

ceRNA regulation (promotes); fibrosis (promotes); other pathway/process (promotes)

Detected method:
Q
H
Validation methods:

RT-qPCR; FISH / smFISH; Clinical Sample Validation; In Vivo Animal Model; Bioinformatics Analysis

Clinical significance:

circZNF609 expression increased in renal biopsies of FSGS patients and may be a novel therapeutic target for FSGS.

Description:

circZNF609 is up-regulated in Adriamycin-induced FSGS mouse kidneys, BSA-exposed HK-2 cells, and renal biopsies from FSGS patients. The study suggests that circZNF609 contributes to FSGS pathogenesis through a circZNF609/miR-615-5p/COL1 ceRNA mechanism, promoting podocyte injury and renal fibrosis.

Confidence score:

0.4997

Other information
Title:

CircZNF609 is involved in the pathogenesis of focal segmental glomerulosclerosis by sponging miR-615-5p.

Journal: Biochemical and biophysical research communications
Published: 2020
PubMed ID: 32800553
Study type:

combined biological and clinical study

Data availability: https://doi.org/10.1016/j.bbrc.2020.07.066
Code availability: -