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Preparation and In Vitro Characterization of Magnetized miR-modified Endothelial Cells
Published on: May 2, 2017
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EBV miR-BART10-3p Promotes Cell Proliferation and Migration by Targeting DKK1
Kyoungmi Min1, Suk Kyeong Lee1
1Department of Biomedicine & Health Sciences, Department of Medical Lifescience, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
International Journal of Biological Sciences
|February 13, 2019
Summary
Epstein-Barr virus (EBV)-associated gastric cancer involves BART miRNAs. miR-BART10-3p targets DKK1, influencing tumor progression by regulating cell proliferation and migration.
Area of Science:
- Molecular Biology
- Oncology
- Virology
Background:
- Epstein-Barr virus (EBV) infection is linked to epithelial cancers.
- BamHI A rightward transcript (BART) miRNAs are highly expressed in EBV-infected cancers.
- Limited knowledge exists regarding BART miRNA target genes in these cancers.
Purpose of the Study:
- To investigate the role of miR-BART10-3p in EBV-associated gastric carcinoma (EBVaGC).
- To determine if miR-BART10-3p directly targets DKK1.
- To explore the impact of the miR-BART10-3p/DKK1 axis on cancer cell behavior.
Main Methods:
- mRNA microarray analysis to identify differentially expressed genes.
- Luciferase reporter assay to confirm direct targeting of DKK1 3'-UTR by miR-BART10-3p.
- Transfection experiments using miR-BART10-3p mimics, inhibitors, siDKK1, and DKK1 overexpression vectors.
Main Results:
- DKK1 expression was significantly downregulated in EBVaGC cells.
- miR-BART10-3p directly targets and downregulates DKK1.
- miR-BART10-3p and siDKK1 promoted cell proliferation and migration.
- Inhibition of miR-BART10-3p or DKK1 overexpression suppressed proliferation and migration.
Conclusions:
- miR-BART10-3p plays a role in EBVaGC progression by targeting DKK1.
- The miR-BART10-3p/DKK1 pathway influences cancer cell proliferation and migration.
- This study identifies a novel regulatory mechanism in EBV-associated gastric cancer.
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