Related Experiment Video
Updated: Oct 29, 2025

Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer
Published on: May 10, 2024
CircCSNK1G1 Contributes to the Tumorigenesis of Gastric Cancer by Sponging miR-758 and Regulating ZNF217 Expression
1Department of Gastroenterology, the First People's Hospital of Huzhou, Huzhou, 313000, People's Republic of China.
Background:
Increasing evidence indicates that circular RNAs (circRNAs) act as vital regulators in various cancers. Nevertheless, the effect of circCSNK1G1 on gastric cancer (GC) is still unknown.
Methods:
The mRNA levels of circCSNK1G1, miR-758, and ZNF217 were measured by RT-qPCR. The protein levels of ZNF217 were evaluated by Western blotting. Cell migration, invasion, proliferation, and apoptosis were detected by Transwell, CCK-8, and flow cytometry assays. The association between miR-758 and circCSNK1G1/ZNF217 was confirmed by RIP and luciferase reporter assays. Xenograft assay was employed for in vivo experiment.
Results:
In the current study, it was demonstrated that the expression levels of circCSNK1G1 and ZNF217 were upregulated in GC tissues and cells, while the level of miR-758 was declined. Furthermore, functional assays indicated that circCSNK1G1 depletion suppressed GC progression in vitro and in vivo. In addition, circCSNK1G1 directly interacted with miR-758, and the supplementation of miR-758 suppressed the development of GC, which was abolished following pcDNA3.1-circCSNK1G1 transfection. Then, we explored the downstream mechanism of miR-758 and found that miR-758 could target the 3'UTR of ZNF217 mRNA. The overexpression of miR-758 neutralized the ZNF217-mediated effects on facilitating the progression of GC. Finally, we revealed that circCSNK1G1 could upregulate ZNF217 expression by sponging miR-758 in GC cells.
Conclusion:
Our study revealed that circCSNK1G1 accelerated GC progression via the miR-758/ZNF217 axis, suggesting that circCSNK1G1 might be a potential biomarker for GC diagnosis and treatment.
Insights
Circular RNAs (circRNAs) regulate cancer. This study shows circCSNK1G1 accelerates gastric cancer (GC) by sponging miR-758, upregulating ZNF217, indicating circCSNK1G1 is a potential GC biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are increasingly recognized as key regulators in diverse cancers.
- The specific role of circCSNK1G1 in gastric cancer (GC) remains largely unexplored.
Purpose of the Study:
- To investigate the function and mechanism of circCSNK1G1 in gastric cancer progression.
- To explore the potential of circCSNK1G1 as a diagnostic and therapeutic target for GC.
Main Methods:
- Quantitative real-time PCR (RT-qPCR) and Western blotting were used to assess gene and protein expression.
- In vitro assays (Transwell, CCK-8, flow cytometry) and in vivo xenograft assays evaluated GC cell behavior.
- RNA immunoprecipitation (RIP) and luciferase reporter assays confirmed molecular interactions.
Main Results:
- circCSNK1G1 and ZNF217 were upregulated, while miR-758 was downregulated in GC tissues and cells.
- circCSNK1G1 depletion inhibited GC progression both in vitro and in vivo.
- circCSNK1G1 acts as a sponge for miR-758, leading to increased ZNF217 expression and promoting GC development.
Conclusions:
- circCSNK1G1 accelerates gastric cancer progression through the miR-758/ZNF217 signaling axis.
- circCSNK1G1 presents a promising potential biomarker for GC diagnosis and therapeutic intervention.
More Related Videos
09:24Combined Conditional Knockdown and Adapted Sphere Formation Assay to Study a Stemness-Associated Gene of Patient-derived Gastric Cancer Stem Cells
Published on: May 9, 2020
09:45Mosaic Zebrafish Transgenesis for Functional Genomic Analysis of Candidate Cooperative Genes in Tumor Pathogenesis
Published on: March 31, 2015
Related Concept Videos
Abnormal Proliferation
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Tumor Microenvironment
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Mitogens and the Cell Cycle