circRNA basic information
circBase ID: -
Name: hsa_circ_SLIT2
Synonym: circSLIT2
Host Gene: SLIT2
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:

GC tissues; paired non-tumor tissues; plasma samples

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: -
Biological function: Potential diagnostic and prognostic biomarker for gastric cancer; increased circSLIT2 RNA accumulation is associated with distant tumor metastases, while functional assays were not performed.
Molecular mechanism: Underlying mechanisms were not experimentally explored in this study.
Biological pathway or process:

metastasis (other)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Cohort Study; Survival Analysis; ROC Analysis

Clinical significance:

Increased plasma circSLIT2 may serve as a biomarker for GC diagnosis and prognosis; high circSLIT2 levels in plasma and tumor tissues were observed in most patients who died during follow-up.

Description:

circSLIT2 is up-regulated in gastric cancer tissues and plasma, with plasma levels positively correlated with tumor-tissue levels. The study supports circSLIT2 as a diagnostic and prognostic biomarker for gastric cancer, with high expression associated with poorer survival and distant metastasis, but it did not experimentally define a molecular mechanism.

Confidence score:

0.4992

Other information
Title:

CircRNA circSLIT2 is a novel diagnostic and prognostic biomarker for gastric cancer.

Journal: Wiener klinische Wochenschrift
Published: 2023
PubMed ID: 37074418
Study type:

combined biological and clinical study

Data availability: The analyzed data sets generated during the study are available from the corresponding author on reasonable request.
Code availability: -