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Updated: Dec 3, 2025

MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues
Published on: November 30, 2013
LINC02738 Participates in the Development of Kidney Cancer Through the miR-20b/Sox4 Axis
1Department of Urology, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, People's Republic of China.
Background:
Long non-coding RNAs (lncRNAs) can affect tumorigenesis. Data from The Cancer Genome Atlas (TCAG) suggest that LINC02783 is highly expressed in renal cell carcinoma (RCC) and is expected to be a potential biological target. We conducted this study to verify this.
Patients And Methods:
We conducted this study to verify the opinion that "LINC02783 is highly expressed in renal cell carcinoma (RCC) and is expected to be a potential biological target". We employed quantitative real-time polymerase chain reaction (qRT-PCR) to test LINC02783 expression in RCC tissues, CKK-8 assay and transwell assay to assess the viability and invasion of RCC cells, Western blot to quantify Sox-4 expression, dual-luciferase reporter (DLR) assay and RNA immunoprecipitation (RIP) assay to analyze the interaction between LINC02783 and miR-20b, in vivo experiments to test tumor formation.
Results:
We detected high LINC02783 expression in RCC patients. Patients with higher LINC02783 levels had a markedly poorer prognosis. In vitro and in vivo, the down-regulation of LINC02783 suppressed the viability and invasion of RCC cells. The DLR assay results revealed that LINC02783 enhanced Sox-4 expression by regulating miR-20b. LINC02783 can act as a sponge for miR-20b to inhibit Sox-4 expression.
Conclusion:
LINC02783 is highly expressed in RCC patients and indicates a poor prognosis. LINC02783 can affect the occurrence and progression of RCC through the miR-20b/Sox-4 axis, making it a promising target for the treatment of RCC.
Insights
High expression of LINC02783 in renal cell carcinoma (RCC) correlates with poor prognosis. This long non-coding RNA promotes RCC progression via the miR-20b/Sox-4 pathway, suggesting it as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) play a role in tumorigenesis.
- The Cancer Genome Atlas (TCGA) data indicate elevated LINC02783 expression in renal cell carcinoma (RCC).
- LINC02783 is a potential therapeutic target in RCC.
Purpose of the Study:
- To verify the high expression of LINC02783 in RCC.
- To investigate the role of LINC02783 in RCC progression.
- To explore the underlying molecular mechanism of LINC02783 in RCC.
Main Methods:
- Quantitative real-time polymerase chain reaction (qRT-PCR) for LINC02783 expression.
- Cell viability (CCK-8) and invasion (Transwell) assays.
- Western blot, dual-luciferase reporter (DLR) assay, RNA immunoprecipitation (RIP), and in vivo tumor formation experiments.
Main Results:
- LINC02783 was highly expressed in RCC tissues, correlating with poorer patient prognosis.
- Downregulation of LINC02783 inhibited RCC cell viability and invasion in vitro and in vivo.
- LINC02783 acts as a molecular sponge for miR-20b, thereby enhancing Sox-4 expression.
Conclusions:
- LINC02783 is upregulated in RCC and associated with poor prognosis.
- LINC02783 promotes RCC occurrence and progression through the miR-20b/Sox-4 axis.
- LINC02783 represents a promising therapeutic target for RCC treatment.
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