circRNA basic information
circBase ID: hsa_circ_0063526
Name: hsa_circ_RanGAP1
Synonym: -
Host Gene: RanGAP1
Genomic location(hg19): chr22:41650311-41677086:-
Genomic location(hg38): chr22:41254307-41281082:-
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005133
MONDO name: endometriosis
Disease details: endometriosis
Disease DO ID:
289
Disease MeSH ID:
D004715
Disease NCIt ID:
C3014
Disease ICD11 ID:
1838213761
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

ectopic endometrial tissue; endometriosis lesions; eutopic endometrial tissue

Cell lines:

End1/E6E7; HEK293T

In vivo animal model:

patient-derived xenograft

circRNA-disease information
Expression pattern:
UP
Associated gene: ER-alpha, ER-beta
Associated microRNA: miR-141-5p
Biological function: promotes endometriosis progression by enhancing proliferation, invasion, and migration; knockdown reduces lesion size in vivo
Molecular mechanism: hsa_circ_0063526 binds (sponges) miR-141-5p; impacts EMT markers and downregulates estrogen receptors
Biological pathway or process:

EMT (promotes); migration (promotes); invasion (promotes); proliferation (promotes); ceRNA regulation (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Bioinformatics Analysis; Luciferase Reporter Assay; Transfection; Transwell Assay; Wound Healing Assay; EdU Staining; ELISA; In Vivo Animal Model; H&E Staining; IHC (Immunohistochemistry); Clinical Sample Validation

Clinical significance:

possible biomarkers and therapeutic targets for endometriosis

Description:

hsa_circ_0063526 is up-regulated in endometriosis ectopic lesions. It promotes endometriosis cell proliferation, invasion and migration by binding miR-141-5p and enhancing EMT-related changes, and its knockdown reduces lesion size and suppresses estrogen receptor expression in vivo.

Confidence score:

0.713

Other information
Title:

Knockdown hsa_circ_0063526 inhibits endometriosis progression via regulating the miR-141-5p / EMT axis and downregulating estrogen receptors.

Journal: Aging
Published: 2021
PubMed ID: 34967761
Study type:

combined biological and clinical study

Data availability: All data are available to others with investigator support.
Code availability: -