circRNA basic information
circBase ID: -
Name: hsa_circ_PVT1
Synonym: circular RNA PVT1 / circ-PVT1
Host Gene: PVT1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005140
MONDO name: ovarian carcinoma
Disease details: epithelial ovarian cancer / EOC
Disease DO ID:
4001
Disease MeSH ID:
-
Disease NCIt ID:
C4908
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

CAOV3; SKOV3; SNU119; OVCAR3; HOSEpiC; 293T

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: miR-149
Biological function: Circ-PVT1 enhances epithelial ovarian cancer cell proliferation and inhibits cell apoptosis.
Molecular mechanism: Circ-PVT1 directly sponges miR-149 and negatively regulates miR-149 in EOC cells.
Biological pathway or process:

proliferation (promotes); apoptosis (inhibits); ceRNA regulation (other)

Detected method:
Q
Validation methods:

RNase R Treatment; RT-qPCR; Transfection; CCK8; Annexin V/PI Flow Cytometry; Luciferase Reporter Assay; Bioinformatics Analysis

Clinical significance:

circ-PVT1 may serve as a treatment target in EOC.

Description:

In this study, circ-PVT1 was up-regulated in human epithelial ovarian cancer cell lines compared with normal ovarian surface epithelial cells. Functional assays showed that circ-PVT1 promotes EOC cell proliferation and inhibits apoptosis. Mechanistically, circ-PVT1 directly sponges and negatively regulates miR-149, suggesting a potential therapeutic target role in EOC.

Confidence score:

0.6263

Other information
Title:

Circular RNA PVT1 enhances cell proliferation but inhibits apoptosis through sponging microRNA-149 in epithelial ovarian cancer.

Journal: The journal of obstetrics and gynaecology research
Published: 2020
PubMed ID: 32048451
Study type:

biological research

Data availability: Additional Supporting Information may be found in the online version of this article at the publisher's web-site
Code availability: -