circRNA basic information
circBase ID: -
Name: hsa_circ_SMAD7
Synonym: circ-SMAD7 / CircRNA SMAD7
Host Gene: SMAD7
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0021042
MONDO name: glioma
Disease details: glioma
Disease DO ID:
-
Disease MeSH ID:
D005910
Disease NCIt ID:
C3059
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

glioma tissues; adjacent tissues

Cell lines:

U87; U373; U251; T98; normal human astrocyte 1800 cell line

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: PCNA
Associated microRNA: -
Biological function: promotes glioma cell proliferation, cell cycle progression, migration, invasion, metastasis, and tumorigenesis
Molecular mechanism: circ-SMAD7 promotes glioma progression by upregulating PCNA mRNA and protein expression
Biological pathway or process:

proliferation (promotes); cell cycle (promotes); migration (promotes); invasion (promotes); metastasis (promotes); other pathway/process (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; CCK8; Cell Cycle Assay; Transwell Assay; Western Blot

Clinical significance:

circ-SMAD7 expression was associated with patients' WHO stage and KPS score; circ-SMAD7/PCNA might be a novel therapeutic strategy in glioma

Description:

circ-SMAD7 is up-regulated in glioma tissues and glioma cell lines. Functional knockdown experiments indicate that circ-SMAD7 promotes glioma cell proliferation, cell-cycle progression, migration, and invasion, likely through upregulating PCNA expression. Its expression is associated with WHO stage and KPS score, suggesting potential clinical relevance as a therapeutic target.

Confidence score:

0.5414

Other information
Title:

Circular RNA circ-SMAD7 promoted glioma cell proliferation and metastasis by upregulating PCNA.

Journal: European review for medical and pharmacological sciences
Published: 2019
PubMed ID: 31799673
Study type:

combined biological and clinical study

Data availability: -
Code availability: -