circRNA basic information
circBase ID: hsa_circ_0060467
Name: hsa_circ_MYBL2
Synonym: -
Host Gene: MYBL2
Genomic location(hg19): chr20:42338602-42345122:+
Genomic location(hg38): chr20:43709962-43716482:+
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0002974
MONDO name: cervical cancer
Disease details: cervical cancer
Disease DO ID:
4362
Disease MeSH ID:
-
Disease NCIt ID:
C9311
Disease ICD11 ID:
1256072522
Disease OMIM ID:
603956
Species: Human
Species details: Homo sapiens
Tissue specimen:

CC tissues; adjacent normal tissues (ANT)

Cell lines:

HCvEpC; C33A; HeLa; SiHa; CaSki; C4‐1

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: miR-361-3p
Biological function: promotes proliferation; promotes invasion; promotes epithelial-mesenchymal transition (EMT)
Molecular mechanism: Acts as a miRNA sponge binding miR-361-3p; miR-361-3p suppression rescues phenotypes caused by circ-MYBL2 knockdown.
Biological pathway or process:

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

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Survival Analysis; Bioinformatics Analysis; Luciferase Reporter Assay; RNA Pull-Down; Transfection; CCK8; Colony Formation Assay; Transwell Assay; Western Blot

Clinical significance:

High circ-MYBL2 expression was associated with advanced FIGO stage, larger tumor size, lymph node metastasis, and poor prognosis in CC patients.

Description:

circ-MYBL2 (hsa_circ_0060467) is up-regulated in cervical cancer and promotes malignant phenotypes (proliferation, invasion, EMT). Mechanistically, it functions as a sponge for miR-361-3p, and miR-361-3p inhibition rescues the effects of circ-MYBL2 knockdown. High circ-MYBL2 expression is associated with advanced clinical features and poor prognosis.

Confidence score:

0.7537

Other information
Title:

circ-MYBL2 Serves As A Sponge For miR-361-3p Promoting Cervical Cancer Cells Proliferation And Invasion.

Journal: OncoTargets and therapy
Published: 2019
PubMed ID: 31819492
Study type:

combined biological and clinical study

Data availability: The dataset supporting the conclusions of this article is included within the article.
Code availability: -