circRNA basic information
circBase ID: -
Name: hsa_circ_MTHFD2
Synonym: circ MTHFD2 / hsa-circR0003936
Host Gene: MTHFD2
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:

-

Cell lines:

MGC-803; MGC-803/MTA

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DS
Associated gene: TS, ABCC11, RCF1, FDZ5, MDR-1
Associated microRNA: miR-124
Biological function: Circ MTHFD2 enhances pemetrexed/MTA resistance and increases the survival rate of MGC-803/MTA gastric cancer cells.
Molecular mechanism: Circ MTHFD2 functions through a miR-124 molecular sponge mechanism, increasing TS and ABCC11 protein expression and decreasing RCF1 protein expression, thereby enhancing MTA resistance.
Biological pathway or process:

drug resistance (promotes); chemoresistance (promotes); ceRNA regulation (promotes)

Detected method:
Q
M
Validation methods:

Microarray; RT-qPCR; Bioinformatics Analysis; Luciferase Reporter Assay; Transfection; CCK8; Western Blot

Clinical significance:

Circ MTHFD2 may provide a valuable biomarker for MTA resistance and a new drug target for overcoming gastric cancer drug resistance.

Description:

This study identified circ MTHFD2 as a dysregulated circRNA associated with pemetrexed/MTA resistance in gastric cancer MGC-803/MTA cells. Functionally, circ MTHFD2 promoted drug resistance and cell survival, at least partly by binding miR-124 and altering TS, ABCC11, and RCF1 protein expression. The authors propose circ MTHFD2 as a potential biomarker and therapeutic target for overcoming MTA resistance in gastric cancer.

Confidence score:

0.5804

Other information
Title:

Effect of circ MTHFD2 on resistance to pemetrexed in gastric cancer through regulating expression of miR-124.

Journal: European review for medical and pharmacological sciences
Published: 2019
PubMed ID: 31841184
Study type:

biological research

Data availability: http://www.circbase.org/; http://circnet.mbc.nctu.edu.tw/; http://www.targetscan.org/
Code availability: -