circRNA basic information
circBase ID: hsa_circ_0001610
Name: hsa_circ_TNFRSF21
Synonym: circ_0001610
Host Gene: TNFRSF21
Genomic location(hg19): chr6:47251673-47254331:-
Genomic location(hg38): chr6:47283937-47286595:-
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0002447
MONDO name: endometrial carcinoma
Disease details: Endometrial carcinoma
Disease DO ID:
2871
Disease MeSH ID:
-
Disease NCIt ID:
C7558
Disease ICD11 ID:
1123821211
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

EC samples; normal non-neoplastic endometria samples; xenograft tumors

Cell lines:

KLE; Ishikawa; HEC-1B; hEEC

In vivo animal model:

cell line-derived xenograft

circRNA-disease information
Expression pattern:
UP
Associated gene: STAT3
Associated microRNA: miR-646
Biological function: Promotes EC cell proliferation, migration, invasion, glycolysis, cell-cycle progression and xenograft tumor growth, and inhibits apoptosis; knockdown suppresses EC progression.
Molecular mechanism: circ_0001610 acts as a sponge for miR-646 to regulate STAT3 expression, thereby modulating EC progression and glycolysis.
Biological pathway or process:

proliferation (promotes); migration (promotes); invasion (promotes); apoptosis (inhibits); glycolysis (promotes); cell cycle (promotes); ceRNA regulation (other); other pathway/process (promotes)

Detected method:
Q
Validation methods:

RNase R Treatment; RT-qPCR; Clinical Sample Validation; Bioinformatics Analysis; Luciferase Reporter Assay; Transfection; CCK8; Colony Formation Assay; Transwell Assay; Wound Healing Assay; Cell Cycle Assay; Annexin V/PI Flow Cytometry; Western Blot; In Vivo Animal Model

Clinical significance:

circ_0001610 is upregulated in EC clinical samples and may provide a potential strategy for EC therapy.

Description:

hsa_circ_0001610/circ_0001610 is upregulated in endometrial carcinoma tissues and cell lines. Its knockdown suppresses EC progression by reducing proliferation, migration, invasion, glycolysis and xenograft tumor growth while increasing apoptosis, at least partly through the miR-646-STAT3 regulatory axis.

Confidence score:

0.7184

Other information
Title:

hsa_circ_0001610 knockdown modulates miR-646-STAT3 axis to suppress endometrial carcinoma progression.

Journal: The journal of gene medicine
Published: 2021
PubMed ID: 33822442
Study type:

combined biological and clinical study

Data availability: The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Code availability: -