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Updated: Dec 3, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-142-5p promotes renal cell tumorigenesis by targeting TFAP2B
Maoshu Zhu1, Liangneng Zou2, Fuhua Lu3
1The Central Laboratory, The Fifth Hospital of Xiamen, Xiamen, Fujian 361101, P.R. China.
Abstract:
The transcription factor AP-2 β (TFAP2B) serves an important role in kidney development. MicroRNAs (miRNAs) regulate carcinogenic pathways and have gained increasing attention owing to their association with human clear cell renal cell carcinoma (ccRCC) tumorigenesis. However, whether miRNAs could affect renal cell tumorigenesis by regulating TFAP2B expression has not been identified. The aim of this study was to investigate the effects of miRNA on TFAP2B and its potential role in cell growth, invasion and migration. PCR, western blot and dual luciferase reporter assays were performed to analyze the effects of miR-142-5p on TFAP2B. Furthermore, MTT, flow cytometry, wound healing and Transwell migration assays were used to analyze the effect of miR-142-5p on cell proliferation and migration. The results demonstrated that miR-142-5p targeted TFAP2B and downregulated the expression of TFAP2B at the mRNA and protein levels, promoting cell proliferation and migration in two ccRCC cell lines, 786-O and A-498. This phenomenon supported the theory that miR-142-5p may function as an oncogene in ccRCC. The potential clinical significance of miR-142-5p as a biomarker and a therapeutic target provides rationale for further investigation into miR-142-5p-mediated molecular pathways and how these may be associated with ccRCC development.
Insights
MicroRNA-142-5p targets TFAP2B, promoting clear cell renal cell carcinoma (ccRCC) cell growth and migration. This suggests miR-142-5p acts as an oncogene in ccRCC development.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Transcription factor AP-2 beta (TFAP2B) is crucial for kidney development.
- MicroRNAs (miRNAs) are implicated in cancer, including clear cell renal cell carcinoma (ccRCC).
- The regulatory relationship between miRNAs and TFAP2B in ccRCC remains unclear.
Purpose of the Study:
- To investigate the effect of miRNAs on TFAP2B expression.
- To explore the role of miRNA-TFAP2B interaction in ccRCC cell proliferation, invasion, and migration.
Main Methods:
- Polymerase Chain Reaction (PCR) and Western Blotting to assess TFAP2B expression.
- Dual Luciferase Reporter Assays to confirm miRNA targeting.
- MTT assays, Flow Cytometry, Wound Healing, and Transwell assays to evaluate cell behavior.
Main Results:
- miR-142-5p was identified as a regulator of TFAP2B.
- miR-142-5p significantly downregulated TFAP2B expression at both mRNA and protein levels.
- miR-142-5p promoted proliferation and migration in ccRCC cell lines (786-O and A-498).
Conclusions:
- miR-142-5p targets TFAP2B and promotes ccRCC progression.
- miR-142-5p may function as an oncogene in ccRCC.
- miR-142-5p holds potential as a biomarker and therapeutic target for ccRCC.
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