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Updated: Mar 29, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Tumor suppressive microRNA‑429 regulates cellular function by targeting VEGF in clear cell renal cell carcinoma
Duqun Chen1, Yuchi Li2, Yifan Li1
1Department of Urology, Peking University Shenzhen Hospital, Institute of Urology of Shenzhen PKU‑HKUST Medical Center, Shenzhen, Guangdong 518036, P.R. China.
Abstract:
Clear cell renal cell carcinoma (ccRCC) is the predominant and most aggressive type of kidney malignancy, however, the mechanism underlying its carcinogenesis remains to be elucidated. The present study aimed to determine the expression and function of microRNA (miR)‑429 in ccRCC carcinogenesis. Reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) was used to detect the expression of miR‑429 in ccRCC specimens. Following transfection of miR‑429 synthetic mimics, the expression of miR‑429 was examined and cell proliferation, cell migration, apoptosis and luciferase assays were conducted in ccRCC cell lines. The results demonstrated that expression of miR‑429 was decreased in ccRCC cells. In addition, upregulation of miR‑429 by transfection of mimics reduced cellular proliferation and migration, and induced apoptosis in ACHN and 786‑0 cell lines. Furthermore, miR‑429 decreased the 3'UTR luciferase activity of vascular endothelial growth factor (VEGF) and c‑MYC, and RT‑qPCR analysis demonstrated that the cancer cells transfected with miR‑429 mimics exhibited decreased expression of VEGF, but not c‑MYC. To the best of our knowledge, the present study was the first to reveal that downregulated miR‑429 functioned as a tumor suppressor by restraining cellular proliferation and migration, and inducing apoptosis, as well as targeting VEGF in ccRCC cells.
Insights
MicroRNA-429 (miR-429) is downregulated in clear cell renal cell carcinoma (ccRCC), acting as a tumor suppressor. Upregulating miR-429 inhibits ccRCC cell proliferation and migration while promoting apoptosis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Clear cell renal cell carcinoma (ccRCC) is the most common and aggressive kidney cancer subtype.
- The molecular mechanisms driving ccRCC development are not fully understood.
Purpose of the Study:
- To investigate the expression and functional role of microRNA (miR)-429 in ccRCC carcinogenesis.
- To identify potential targets of miR-429 in ccRCC.
Main Methods:
- Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to measure miR-429 expression.
- Transfection of ccRCC cell lines (ACHN and 786-0) with miR-429 mimics.
- Assays for cell proliferation, migration, apoptosis, and luciferase activity.
Main Results:
- miR-429 expression was significantly decreased in ccRCC tissues and cell lines.
- Overexpression of miR-429 suppressed ccRCC cell proliferation and migration.
- miR-429 upregulation induced apoptosis in ccRCC cells.
- miR-429 directly targeted the 3' untranslated region (3'UTR) of vascular endothelial growth factor (VEGF) mRNA, reducing its expression.
Conclusions:
- Downregulated miR-429 acts as a tumor suppressor in ccRCC.
- miR-429 restrains ccRCC cell proliferation and migration, and induces apoptosis.
- VEGF is a direct target of miR-429 in ccRCC, suggesting a role in tumor progression.
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