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Updated: Dec 17, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
MiRNA-1246 suppresses the proliferation and migration of renal cell carcinoma through targeting CXCR4
1Department of Urology Surgery, Daqing Oilfield General Hospital, Daqing, China. fanwx1999@163.com.
Objective:
To uncover the role of miRNA-1246 in influencing the proliferative and migratory capacities of RCC by binding CXCR4 and downregulating its level.
Patients And Methods:
Relative levels of miRNA-1246 and CXCR4 in 40 paired RCC tissues and adjacent normal tissues were determined. The binding relationship between miRNA-1246 and CXCR4 was confirmed by Dual-Luciferase reporter assay. Proliferative and migratory abilities of RCC regulated by miRNA-1246 and CXCR4 were assessed.
Results:
MiRNA-1246 was downregulated in RCC tissues and cell lines. Overexpression of miRNA-1246 attenuated proliferative and migratory capacities of 786-O and 769-P cells. CXCR4 was the direct target of miRNA-1246 and its level was negatively regulated by miRNA-1246. Silence of CXCR4 inhibited RCC to proliferate and migrate.
Conclusions:
MiRNA-1246 attenuates proliferative and migratory abilities of RCC by downregulating CXCR4. MiRNA-1246/CXCR4 axis could be potential therapeutic target for RCC.
Insights
MicroRNA-1246 (miRNA-1246) is downregulated in renal cell carcinoma (RCC), suppressing tumor growth and migration by targeting CXCR4. This miRNA-1246/CXCR4 interaction presents a potential therapeutic strategy for RCC.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Renal cell carcinoma (RCC) is a significant global health concern.
- Understanding the molecular mechanisms driving RCC proliferation and metastasis is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of microRNA-1246 (miRNA-1246) in regulating the proliferative and migratory capacities of RCC.
- To elucidate the interaction between miRNA-1246 and CXCR4 in RCC pathogenesis.
Main Methods:
- Quantitative analysis of miRNA-1246 and CXCR4 expression in 40 paired RCC and normal tissues.
- Dual-Luciferase reporter assay to confirm the binding relationship between miRNA-1246 and CXCR4.
- Assessment of RCC cell proliferation and migration following miRNA-1246 or CXCR4 manipulation.
Main Results:
- MiRNA-1246 was found to be significantly downregulated in RCC tissues and cell lines.
- Overexpression of miRNA-1246 inhibited the proliferation and migration of RCC cells (786-O and 769-P).
- CXCR4 was identified as a direct target of miRNA-1246, with its expression negatively regulated by miRNA-1246. Silencing CXCR4 also inhibited RCC proliferation and migration.
Conclusions:
- MiRNA-1246 suppresses RCC proliferation and migration by downregulating CXCR4.
- The miRNA-1246/CXCR4 axis represents a promising therapeutic target for renal cell carcinoma.
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