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Updated: Mar 30, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-490-5p suppresses tumour growth in renal cell carcinoma through targeting PIK3CA
Ke Chen1,2, Jin Zeng1,2, Kun Tang1,2
1Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, PR China.
Background Information:
Dysregulated micro-RNAs have been reported in many human cancers, including renal cell carcinoma. Recent studies indicated that miR-490 is involved in tumour development and progression. However, the expression profile and function in renal cell carcinoma remains unknown.
Results:
Herein, we showed that miR-490-5p was down-regulated in renal cell carcinoma tissues and cells compared with the adjacent normal tissues and normal cells. We also provided evidence that miR-490-5p acts as a tumour suppressor in renal carcinoma in a variety of in vitro and in vivo assays. Mechanistically, miR-490-5p was verified to directly bind to 3' UTR of the PIK3CA mRNA and reduce the expression of PIK3CA at both mRNA and protein levels, which further inhibits phosphatidylinositol 3-kinase/Akt signalling pathway. We further showed that knockdown of PIK3CA can block the growth inhibitory effect of miR-490-5p, and over-expression of PIK3CA can reverse the inhibitory effect of miR-490-5p on renal cancer cell tumourigenicity.
Conclusions:
Taken together, our results indicated for the first time that miR-490-5p functions as a tumour suppressor in renal carcinoma by targeting PIK3CA.
Significance:
Our findings suggest that miR-490-5p may be a potential gene therapy target for the treatment of renal cell carcinoma.
Insights
MicroRNA-490-5p is downregulated in renal cell carcinoma, acting as a tumor suppressor by targeting PIK3CA. This finding suggests miR-490-5p as a potential therapeutic target for kidney cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are implicated in various human cancers, including renal cell carcinoma (RCC).
- The specific role and expression of miR-490 in RCC progression were previously unknown.
- Emerging evidence suggests miR-490's involvement in tumor development.
Purpose of the Study:
- To investigate the expression profile of miR-490 in renal cell carcinoma.
- To elucidate the functional role of miR-490 in RCC.
- To identify the molecular targets and pathways regulated by miR-490 in RCC.
Main Methods:
- Quantitative real-time PCR to assess miR-490-5p expression in RCC tissues and cells.
- In vitro assays (e.g., cell proliferation, migration) and in vivo xenograft models to evaluate tumor suppressor activity.
- Luciferase reporter assays and Western blotting to confirm direct binding of miR-490-5p to PIK3CA mRNA and its effect on protein levels.
- Gene knockdown and overexpression studies to validate the mechanistic link between miR-490-5p and PIK3CA.
Main Results:
- miR-490-5p expression was significantly downregulated in RCC tissues and cells compared to normal controls.
- miR-490-5p demonstrated tumor suppressor functions in multiple in vitro and in vivo assays.
- miR-490-5p directly targets the 3' UTR of PIK3CA mRNA, reducing PIK3CA expression and inhibiting the PI3K/Akt signaling pathway.
- Knockdown of PIK3CA abolished the tumor-inhibitory effects of miR-490-5p, while PIK3CA overexpression reversed these effects.
Conclusions:
- miR-490-5p acts as a tumor suppressor in renal cell carcinoma by targeting PIK3CA.
- The miR-490-5p/PIK3CA axis plays a critical role in regulating RCC cell tumorigenicity.
- miR-490-5p represents a potential therapeutic target for gene therapy in renal cell carcinoma treatment.
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