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Long non-coding RNA SNHG3 promotes the progression of clear cell renal cell carcinoma via regulating BIRC5 expression
Zhaoyu Xu1, Junjie Ye1, Pengfei Bao1
1Department of Urology, Lishui People's Hospital, Lishui, China.
Background:
Research has shown that the progression of clear cell renal cell carcinoma (ccRCC) is modulated by long non-coding RNAs (lncRNAs). However, the roles of specific lncRNAs in the malignancy of ccRCC are still unknown.
Methods:
TCGA and GSE66272 datasets were used to predict differentially expressed genes (DEGs) in ccRCC. ENCORI database was employed to display BIRC5 miRNA network and potential lncRNA interactions for miRNAs. KM plotter and correlation analyses were performed to identify the overall survival (OS)- and BIRC5-related miRNAs. Quantitative real-time PCR (qRT-PCR) was used to verify the BIRC5 mRNA in the seventy paired clinical samples of ccRCC tissues. The ccRCC A498 and 786-O were individually transfected with lncRNA SNHG3 and LINC00997 and then western blotting was used to detect the BIRC5 protein expression. The Dual-luciferase reporter assay was used to examine the regulatory interaction between lncRNA SNHG3 and microRNA (miRNA/miR)-10b-5p.
Results:
BICR5 is associated with the progression of ccRCC. The two novel lncRNAs (LINC00997, SNHG3) were up-regulated in ccRCC tissues and positively with the BICR5 protein expression. However, Suppressing SNHG3 expression reduced BIRC5 protein expression compared with the LINC00997, most importantly, Suppressing SNHG3 expression suppressed tumor progression in vitro. In addition, SNHG3 promotes the expression of BIRC5 protein by sponging microRNA-10b-5p.
Conclusions:
Our findings suggest that SNHG3 plays a vital role in promoting ccRCC via the microRNA-10b-5p/BIRC5 axis and may serve as a novel therapeutic target for the treatment of patients with ccRCC.
Insights
Long non-coding RNA SNHG3 promotes clear cell renal cell carcinoma (ccRCC) progression by interacting with microRNA-10b-5p and upregulating BIRC5. SNHG3 may be a novel therapeutic target for ccRCC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Clear cell renal cell carcinoma (ccRCC) progression is influenced by long non-coding RNAs (lncRNAs).
- The specific roles of lncRNAs in ccRCC malignancy remain largely unknown.
Purpose of the Study:
- To investigate the role of novel lncRNAs in ccRCC progression.
- To elucidate the molecular mechanisms underlying ccRCC malignancy involving lncRNAs and BIRC5.
Main Methods:
- Utilized TCGA and GSE66272 datasets to identify differentially expressed genes in ccRCC.
- Employed ENCORI database for miRNA network analysis and assessed lncRNA-miRNA interactions.
- Performed quantitative real-time PCR, western blotting, and dual-luciferase reporter assays to validate findings and interactions.
Main Results:
- Identified two novel lncRNAs, LINC00997 and SNHG3, upregulated in ccRCC tissues and positively correlated with BIRC5 protein expression.
- Suppression of SNHG3 significantly reduced BIRC5 protein levels and inhibited tumor progression in vitro.
- Demonstrated that SNHG3 promotes BIRC5 expression by sponging microRNA-10b-5p.
Conclusions:
- SNHG3 plays a critical role in promoting ccRCC progression through the microRNA-10b-5p/BIRC5 axis.
- SNHG3 represents a potential novel therapeutic target for ccRCC treatment.
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