circRNA basic information
circBase ID: -
Name: hsa_circ_LDLRAD3
Synonym: circRNA LDLRAD3
Host Gene: LDLRAD3
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005233
MONDO name: non-small cell lung carcinoma
Disease details: non-small-cell lung cancer
Disease DO ID:
3908
Disease MeSH ID:
D002289
Disease NCIt ID:
C2926
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

NSCLC tissues; tumor-adjacent normal tissues

Cell lines:

A549; H1299; HCC827; Calu-3; BEAS-2B

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SLC7A5, mTORC1
Associated microRNA: miR-20a-5p
Biological function: promotes proliferation, migration, and invasion of NSCLC cells
Molecular mechanism: acts as a ceRNA sponging miR-20a-5p to upregulate SLC7A5 and activate mTORC1 signaling
Biological pathway or process:

mTORC1 (promotes); proliferation (promotes); migration (promotes); invasion (promotes); ceRNA regulation (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; CCK8; Transwell Assay; Luciferase Reporter Assay; Western Blot; IF (Immunofluorescence); IHC (Immunohistochemistry); Bioinformatics Analysis; Survival Analysis

Clinical significance:

High LDLRAD3 expression is associated with advanced stage (III+IV vs I+II) and lower survival rate in NSCLC patients.

Description:

circRNA LDLRAD3 is up-regulated in NSCLC tissues/cell lines and promotes NSCLC cell proliferation, migration, and invasion. Mechanistically, LDLRAD3 sponges miR-20a-5p to increase SLC7A5 expression and activates the mTORC1 signaling pathway, and high LDLRAD3 expression is associated with worse patient survival.

Confidence score:

0.7396

Other information
Title:

circRNA LDLRAD3 Enhances the Malignant Behaviors of NSCLC Cells via the miR-20a-5p-SLC7A5 Axis Activating the mTORC1 Signaling Pathway.

Journal: Journal of healthcare engineering
Published: 2022
PubMed ID: 35035814
Study type:

combined biological and clinical study

Data availability: The simulation experiment data used to support the findings of this study are available from the corresponding author upon request.
Code availability: -