circRNA basic information
circBase ID: -
Name: hsa_circ_SCARB1
Synonym: CircRNA SCARB1 / Circ-SCARB1
Host Gene: SCARB1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005086
MONDO name: renal cell carcinoma
Disease details: Renal cell carcinoma / RCC
Disease DO ID:
4450
Disease MeSH ID:
D002292
Disease NCIt ID:
-
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

RCC tissues; matched para-cancerous tissues; adjacent normal tissues

Cell lines:

786-O; 769-P; A498; A704; HK-2

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SDC3
Associated microRNA: miR-510-5p
Biological function: Circ-SCARB1 acts as an oncogenic regulator in RCC cells; its knockdown inhibits cell proliferation, migration and invasion, and induces apoptosis.
Molecular mechanism: Circ-SCARB1 functions as a miR-510-5p sponge and up-regulates SDC3 expression through the Circ-SCARB1/miR-510-5p/SDC3 axis.
Biological pathway or process:

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

Detected method:
Q
Validation methods:

RNase R Treatment; RT-qPCR; Clinical Sample Validation; Bioinformatics Analysis; Luciferase Reporter Assay; Transfection; MTT; Annexin V/PI Flow Cytometry; Transwell Assay; Western Blot

Clinical significance:

Circ-SCARB1 is indicated as a potential therapeutic target for RCC.

Description:

Circ-SCARB1 is up-regulated in RCC tissues and cell lines and functions as an oncogenic circRNA. Mechanistically, it sponges miR-510-5p to relieve repression of SDC3, thereby promoting proliferation, migration and invasion while suppressing apoptosis in RCC cells.

Confidence score:

0.7164

Other information
Title:

CircRNA SCARB1 Promotes Renal Cell Carcinoma Progression Via Mir- 510-5p/SDC3 Axis.

Journal: Current cancer drug targets
Published: 2020
PubMed ID: 32271695
Study type:

combined biological and clinical study

Data availability: The data supporting the findings of the article is available upon request to the corresponding author Jijian Sun (276351335@qq.com).
Code availability: -