circRNA basic information
circBase ID: -
Name: hsa_circ_SMAD7
Synonym: -
Host Gene: SMAD7
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0001056
MONDO name: gastric cancer
Disease details: gastric cancer / GC
Disease DO ID:
10534
Disease MeSH ID:
-
Disease NCIt ID:
C9331
Disease ICD11 ID:
1397617262
Disease OMIM ID:
613659
Species: Human
Species details: Homo sapiens
Tissue specimen:

Human GC tissues; adjacent non-tumor tissues

Cell lines:

BGC-823; SGC-7901; HGC-27; MKN-45; GES

In vivo animal model:

cell line-derived xenograft

circRNA-disease information
Expression pattern:
DN
Associated gene: E-cadherin, N-cadherin, Vimentin
Associated microRNA: -
Biological function: Circ-SMAD7 inhibits GC cell migration, invasion, EMT process, and tumor metastasis in vivo.
Molecular mechanism: Upregulation of circ-SMAD7 reverses or suppresses the EMT process by increasing E-cadherin and decreasing N-cadherin and Vimentin.
Biological pathway or process:

migration (inhibits); invasion (inhibits); metastasis (inhibits); EMT (inhibits)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; Wound Healing Assay; Transwell Assay; Western Blot; In Vivo Animal Model

Clinical significance:

Circ-SMAD7 could serve as a prospective therapeutic target for GC.

Description:

Circ-SMAD7 is down-regulated in gastric cancer tissues and cell lines. Its upregulation suppresses GC migration, invasion, and in vivo metastasis, likely by reversing the EMT process through increased E-cadherin and decreased N-cadherin and Vimentin. The study suggests circ-SMAD7 may be a prospective therapeutic target for GC.

Confidence score:

0.5414

Other information
Title:

Upregulation of circular SMAD7 inhibits tumorigenesis of gastric cancer by reversing epithelial-to-mesenchymal transition.

Journal: European review for medical and pharmacological sciences
Published: 2020
PubMed ID: 32096163
Study type:

combined biological and clinical study

Data availability: -
Code availability: -