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miR-21-5p serves as a promoter in renal cell carcinoma progression through ARHGAP24 downregulation
Bin Meng1, Pengfei Wang1, Chaofei Zhao1
1Department of Urology, Area 3, Tangshan Gongren Hospital, LubeiDistrict, No.27 Wenhua Road, Tangshan, Hebei, 063000, People's Republic of China.
Abstract:
Renal cell carcinoma (RCC) is a highly recurrent aggressive tumor. This study works for the regulation of miR-21-5p on RCC cell functions and novel ideas for therapies of RCC. Isoform expression quantification data were offered by The Cancer Genome Atlas Kidney Renal Clear Cell Carcinoma (TCGA-KIRC) to investigate differentially expressed miRNAs. The way miR-21-5p works on biological functions of RCC was examined with MTT and Transwell assays. The downstream targets of miR-21-5p were predicted using bioinformatics analysis. The binding of two researched objects was verified by the dual-luciferase method. TCGA data manifested a considerably high level of miR-21-5p in RCC tissue, while ARHGAP24 was significantly lowly expressed. miR-21-5p bound ARHGAP24 and stimulated RCC cell functions, whereas ARHGAP24 mimic could reverse such promotion. This work observed miR-21-5p, a stimulator in RCC, and it deteriorated this cancer via repressing its downstream target gene ARHGAP24 expression.
Insights
MicroRNA-21-5p (miR-21-5p) promotes renal cell carcinoma (RCC) progression by inhibiting the ARHGAP24 gene. Targeting miR-21-5p may offer new therapeutic strategies for this aggressive cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Renal cell carcinoma (RCC) is an aggressive cancer with high recurrence rates.
- Understanding the molecular mechanisms regulating RCC progression is crucial for developing effective therapies.
Purpose of the Study:
- To investigate the role of microRNA-21-5p (miR-21-5p) in regulating renal cell carcinoma (RCC) cell functions.
- To identify novel therapeutic targets for RCC based on miR-21-5p regulation.
Main Methods:
- Differential expression analysis of miRNAs in RCC using The Cancer Genome Atlas (TCGA) data.
- In vitro assays (MTT, Transwell) to assess the impact of miR-21-5p on RCC cell behavior.
- Bioinformatics analysis and dual-luciferase assays to predict and validate miR-21-5p targets.
Main Results:
- miR-21-5p was significantly upregulated in RCC tissues compared to normal tissues.
- ARHGAP24 was identified as a direct downstream target of miR-21-5p and was significantly downregulated in RCC.
- miR-21-5p promoted RCC cell proliferation and migration, while ARHGAP24 mimic reversed these effects.
Conclusions:
- miR-21-5p acts as an oncogene in RCC by suppressing its target gene ARHGAP24.
- Inhibition of miR-21-5p could be a potential therapeutic strategy for renal cell carcinoma.
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