circRNA basic information
circBase ID: -
Name: hsa_circ_FOXO3
Synonym: -
Host Gene: FOXO3
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005229
MONDO name: bacterial infectious disease with sepsis
Disease details: sepsis
Disease DO ID:
0040085
Disease MeSH ID:
D016470
Disease NCIt ID:
-
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

peripheral blood; PBMCs

Cell lines:

HUVECs

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DS
Associated gene: FOXO3
Associated microRNA: miR-23a
Biological function: Knockdown of circRNA_FOXO3 restores LPS-induced cell viability loss and cytokine dysregulation in HUVECs (anti-inflammatory effect in this in vitro sepsis-like model).
Molecular mechanism: miR-23a binds and suppresses circRNA_FOXO3 (luciferase reporter); circRNA_FOXO3 is involved in the miR-23a/FOXO3 regulatory network affecting inflammatory cytokine responses under LPS stimulation.
Biological pathway or process:

inflammation (inhibits); immune regulation (other); proliferation (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Survival Analysis; Luciferase Reporter Assay; Transfection; ELISA; MTT

Clinical significance:

Genotypes associated with lower circRNA_FOXO3 (rs12196996 GG with rs2232365 AA) correlate with prolonged survival and suppressed severity in ICU-acquired sepsis.

Description:

In ICU-acquired sepsis patient samples, circRNA_FOXO3 expression differs by rs12196996/rs2232365 genotype combinations. Mechanistically, miR-23a suppresses circRNA_FOXO3 (and FOXO3), and circRNA_FOXO3 knockdown alleviates LPS-induced loss of viability and pro-inflammatory cytokine dysregulation in HUVECs, linking this axis to sepsis severity and survival.

Confidence score:

0.6762

Other information
Title:

Effect of circRNA_FOXO3 rs12196996 polymorphism and FOXO3 rs2232365 polymorphism on survival rate and severity of intensive care unit-acquired sepsis.

Journal: Bioengineered
Published: 2022
PubMed ID: 35156517
Study type:

combined biological and clinical study

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