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Published on: March 30, 2019
The Effects of circ_000558/miR-1225-5p/ARL4C on Regulating the Proliferation of Renal Cell Carcinoma Cells
Ling Xia1, Minghuan Ge2, Guang Shan2
1Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei, China.
Abstract:
Renal cell carcinoma (RCC) is one of the top ten tumors over the world. RCC is not sensitive to radiotherapy and chemotherapy. Therefore, it is necessary to find new targets for the treatment. CircRNAs are a special type of noncoding RNAs, which play important roles in many types of cancer. In this study, we found circ_000558 was upregulated in RCC cells, and it elevated the proliferation ability of RCC cells. The relationship between miR-1225-5p and circ_000558 or ARL4C was predicted via circBank and circular RNA interactome and confirmed by dual-luciferase reporter assay. Then, the effects of circ_000558/miR-1225-5p/ARL4C on RCC cell proliferation and apoptosis were assessed by CCK-8 assay. The results revealed that the knockdown of ARL4C significantly reduced RCC cell proliferation and overexpression of circ_000558 could significantly induce RCC cell proliferation after miR-1225-5p treatment further promoted the inhibitory ability of ARL4C knockdown. Overall, our study suggested that circ_000558/miR-1225-5p/ARL4C network was related to the RCC cell proliferation. This finding could provide new targets for the treatment and prognosis of RCC.
Insights
This study identifies circ_000558 as a key player in renal cell carcinoma (RCC) progression. Upregulated circ_000558 promotes RCC cell proliferation, suggesting it as a potential therapeutic target for this challenging cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Renal cell carcinoma (RCC) is a prevalent cancer with limited treatment options.
- Radiotherapy and chemotherapy are ineffective against RCC, necessitating novel therapeutic targets.
- Circular RNAs (circRNAs) are emerging as critical regulators in various cancers, including RCC.
Purpose of the Study:
- To investigate the role of circ_000558 in renal cell carcinoma (RCC) progression.
- To elucidate the regulatory network involving circ_000558, miR-1225-5p, and ARL4C in RCC.
- To assess the potential of this network as a therapeutic target for RCC treatment.
Main Methods:
- Quantitative analysis of circ_000558 expression in RCC cells.
- Bioinformatic prediction and dual-luciferase reporter assays to confirm interactions between circ_000558, miR-1225-5p, and ARL4C.
- Cell proliferation assays (CCK-8) to evaluate the functional impact of circ_000558, miR-1225-5p, and ARL4C.
Main Results:
- Circ_000558 was found to be significantly upregulated in RCC cells.
- Overexpression of circ_000558 promoted RCC cell proliferation.
- Knockdown of ARL4C significantly inhibited RCC cell proliferation, and this effect was enhanced by miR-1225-5p.
- The circ_000558/miR-1225-5p/ARL4C axis was confirmed to influence RCC cell proliferation.
Conclusions:
- The circ_000558/miR-1225-5p/ARL4C regulatory network plays a crucial role in RCC cell proliferation.
- Circ_000558 emerges as a potential therapeutic target for improving the treatment and prognosis of renal cell carcinoma.
- Further research into targeting this circRNA network could lead to novel therapeutic strategies for RCC.
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