circRNA basic information
circBase ID: -
Name: hsa_circ_SMARCA5
Synonym: circ SMARCA5
Host Gene: SMARCA5
Genomic location(hg19): -
Genomic location(hg38): -
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:

cervical cancer tissue; adjacent tissue

Cell lines:

Ect1/E6E7; Hela; HT-3; C33A; CaSki

In vivo animal model:

cell line-derived xenograft

circRNA-disease information
Expression pattern:
DN
Associated gene: SND1, YWHAB
Associated microRNA: -
Biological function: Inhibits proliferation and invasion, promotes apoptosis, and suppresses tumor metastasis in cervical cancer.
Molecular mechanism: circ SMARCA5 binds the RBP SND1 and inhibits SND1 binding to YWHAB, thereby downregulating YWHAB.
Biological pathway or process:

proliferation (inhibits); invasion (inhibits); apoptosis (promotes); metastasis (inhibits); other pathway/process (other)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; CCK8; Transwell Assay; Annexin V/PI Flow Cytometry; Western Blot; RNA Pull-Down; Co-IP; In Vivo Animal Model; Bioinformatics Analysis

Clinical significance:

-

Description:

circ SMARCA5 is down-regulated in cervical cancer tissues/cell lines. Its overexpression suppresses proliferation, invasion, and in vivo tumor growth/metastasis while promoting apoptosis, mechanistically by binding the RBP SND1 and reducing SND1-mediated YWHAB upregulation.

Confidence score:

0.7045

Other information
Title:

Circ SMARCA5 Inhibited Tumor Metastasis by Interacting with SND1 and Downregulating the YWHAB Gene in Cervical Cancer.

Journal: Cell transplantation
Published: 2021
PubMed ID: 33588586
Study type:

combined biological and clinical study

Data availability: All data generated or analyzed during this study are included in this published article.
Code availability: -