circRNA basic information
circBase ID: -
Name: hsa_circ_ZNF609
Synonym: cZNF609
Host Gene: ZNF609
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005386
MONDO name: peripheral arterial disease
Disease details: lower extremity peripheral artery disease
Disease DO ID:
0050830
Disease MeSH ID:
D058729
Disease NCIt ID:
C84496
Disease ICD11 ID:
1821859817
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

ischemic gastrocnemius; plasma

Cell lines:

HUVECs

In vivo animal model:

other disease animal model

circRNA-disease information
Expression pattern:
UP
Associated gene: HIF1alpha, VEGFA
Associated microRNA: -
Biological function: inhibits endothelial angiogenic functions (proliferation, migration, tube formation) and reduces blood flow recovery after ischemia
Molecular mechanism: Exosomal cZFP609 is delivered from VSMCs to ECs and binds HIF1alpha, sequestering it in the cytoplasm to block HIF1alpha nuclear translocation, thereby inhibiting HIF1alpha-driven VEGFA transcription/expression under hypoxia.
Biological pathway or process:

angiogenesis (inhibits); proliferation (inhibits); migration (inhibits); HIF-1 signaling (inhibits); other pathway/process (inhibits)

Detected method:
Q
Validation methods:

RT-qPCR; Nuclear-Cytoplasmic Fractionation; FISH / smFISH; RIP (RNA Immunoprecipitation); RNA Pull-Down; Transfection; BrdU; Wound Healing Assay; Tube Formation Assay; In Vivo Animal Model; Western Blot; IF (Immunofluorescence); H&E Staining; Bioinformatics Analysis

Clinical significance:

Plasma cZNF609 is higher in patients with atherosclerotic or diabetic lower extremity PAD and is associated with reduced ankle-brachial index (ABI), suggesting potential value for assessing severity/blood flow perfusion.

Description:

cZFP609/cZNF609 is increased (notably in VSMC-derived exosomes and in patient plasma) in ischemia/PAD settings and suppresses angiogenesis. It binds HIF1alpha in EC cytoplasm to block nuclear translocation and downstream VEGFA induction, thereby inhibiting EC proliferation, migration, and tube formation; its knockdown improves perfusion recovery in hindlimb ischemia models.

Confidence score:

0.6744

Other information
Title:

Smooth muscle SIRT1 reprograms endothelial cells to suppress angiogenesis after ischemia.

Journal: Theranostics
Published: 2020
PubMed ID: 31938060
Study type:

combined biological and clinical study

Data availability: All the data are available in the article and Supplementary Files, or available from the authors upon request.
Code availability: -