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Updated: Dec 26, 2025

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
MicroRNA Profile Identifies miR-6165 Could Suppress Gastric Cancer Migration and Invasion by Targeting STRN4
Zhu Wang1,2, Yang Li1,2, Jian Cao1
1Department of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Background:
Recent studies showed that aberrant expression of miRNAs causes tumor-suppressing or promoting effects in various cancers including gastric cancer (GC). Our previous studies showed that lots of miRNAs and mRNA expressed differentially in GC and normal tissues. However, the critical miRNAs and mRNA need to be clarified.
Materials And Methods:
Microarray sequencing was used to profile the differential expression of miRNAs and mRNA in GC and normal tissues. Bioinformatics analysis and database prediction were used to search the critical miRNAs and mRNA. Real-time quantitative polymerase chain reaction (RT-qPCR), luciferase reporter assay, immunohistochemistry (IHC), wound healing assay and transwell assay were used to clarify the relationship between the target miRNAs and mRNA. Statistical analysis was used to seek their value of diagnosis and prognosis.
Results:
We identified microRNA-6165 (miR-6165) as a novel cancer-related miRNA in GC through high-throughput microarray sequencing. By bioinformatics analysis and luciferase reporter assay, we found STRN4 was the target of miR-6165. Via a series of cell experiments, we determined that miR-6165 suppressed GC cells migration and invasion by targeting STRN4. Also, we discovered the potential diagnosis and prognosis value of miR-6165 and STRN4.
Conclusion:
It was found that miR-6165 might suppress GC migration and invasion by targeting STRN4 in vitro, and the further research should focus more on the potential diagnosis and prognosis value of miR-6165 and STRN4 in gastric cancer patients.
Insights
MicroRNA-6165 (miR-6165) was identified as a novel player in gastric cancer (GC). This microRNA targets STRN4, suppressing GC cell migration and invasion, and shows potential for diagnosis and prognosis in GC patients.
Area of Science:
- Molecular Oncology
- Cancer Biology
- Genetics
Background:
- Aberrant microRNA (miRNA) expression is implicated in gastric cancer (GC) pathogenesis.
- Previous studies identified differential miRNA and mRNA expression in GC tissues, necessitating identification of key molecules.
- Understanding critical molecular players is crucial for advancing GC diagnosis and treatment.
Purpose of the Study:
- To identify novel microRNAs (miRNAs) and their targets involved in gastric cancer (GC).
- To elucidate the functional role of identified miRNAs in GC cell behavior.
- To evaluate the diagnostic and prognostic potential of key molecules in GC.
Main Methods:
- High-throughput microarray sequencing for miRNA and mRNA profiling in GC and normal tissues.
- Bioinformatics analysis and database prediction to identify miRNA-mRNA interactions.
- Real-time quantitative polymerase chain reaction (RT-qPCR), luciferase reporter assays, immunohistochemistry (IHC), wound healing, and Transwell assays to validate findings.
- Statistical analysis for diagnostic and prognostic value assessment.
Main Results:
- MicroRNA-6165 (miR-6165) was identified as a novel, differentially expressed miRNA in GC.
- Bioinformatics and luciferase assays confirmed STRN4 as a direct target of miR-6165.
- miR-6165 significantly suppressed gastric cancer cell migration and invasion by targeting STRN4 in vitro.
- Both miR-6165 and STRN4 demonstrated potential diagnostic and prognostic value in GC.
Conclusions:
- miR-6165 acts as a tumor suppressor in gastric cancer by targeting STRN4, inhibiting cell migration and invasion.
- Further research is warranted to explore the clinical utility of miR-6165 and STRN4 as diagnostic and prognostic biomarkers for gastric cancer patients.
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