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Updated: Jan 24, 2026

Modeling Spontaneous Metastatic Renal Cell Carcinoma mRCC in Mice Following Nephrectomy
Published on: April 29, 2014
MiR-1294 acts as a tumor suppressor in clear cell renal cell carcinoma through targeting HOXA6
1Department of Urinary Surgery, RenMin Hospital of Huangpi District, the Third Hospital of Jianghan University, Huangpi District, Wuhan, P. R. China. panwei_wh@163.com.
Objective:
Renal cancer represents about 3% of all human cancers. Clear cell renal cell carcinoma (ccRCC) is the main type of renal cancer. MicroRNAs (miRNAs) have been reported to play crucial roles in the carcinogenesis of human cancers. This study was aimed to investigate the expression of miR-1294 and the mechanisms underlying miR-1294-mediated ccRCC progression.
Materials And Methods:
The miR-1294 expression levels in ccRCC cell lines were analyzed by quantified real time-PCR (qRT-PCR). The effect of the miR-1294 expression on the overall survival of ccRCC patients was analyzed by the Kaplan-Meier Plotter. Cell proliferation, colony growth, and cell invasion were examined by cell counting kit-8 assay, colony formation assay, and transwell invasion assay, respectively. The luciferase activity reporter assay and Western blot assay were conducted to validate the connection between miR-1294 and homeobox A6 (HOXA6).
Results:
MiR-1294 was downregulated in ccRCC cell lines and correlated with the poor overall survival of ccRCC patients. The overexpression of miR-1294 inhibits ccRCC cell proliferation, colony growth, and cell invasion. HOXA6 was validated as a target of miR-1294 and negatively regulated by miR-1294. The overexpression of HOXA6 attenuated the miR-1294-mediated effects on ccRCC cellular functions.
Conclusions:
Our results indicated that miR-1294 functions as a tumor suppressor in ccRCC. MiR-1294 suppressed cell proliferation, colony formation, and invasion in ccRCC partially via targeting HOXA6.
Insights
MicroRNA-1294 (miR-1294) acts as a tumor suppressor in clear cell renal cell carcinoma (ccRCC). Downregulation of miR-1294 correlates with poor survival, and its restoration inhibits ccRCC progression by targeting HOXA6.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Renal cancer, primarily clear cell renal cell carcinoma (ccRCC), accounts for 3% of human cancers.
- MicroRNAs (miRNAs) are implicated in cancer development and progression.
- Understanding specific miRNA roles, like miR-1294, is crucial for ccRCC research.
Purpose of the Study:
- To investigate the expression of miR-1294 in ccRCC.
- To elucidate the mechanisms of miR-1294 in ccRCC progression.
- To identify potential therapeutic targets related to miR-1294.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) for miR-1294 expression analysis.
- Kaplan-Meier plotter for survival analysis.
- Cell counting kit-8, colony formation, and transwell invasion assays for cellular functions.
- Luciferase reporter and Western blot assays to validate miR-1294 and HOXA6 interaction.
Main Results:
- miR-1294 was found to be downregulated in ccRCC cell lines.
- Lower miR-1294 expression correlated with poorer overall survival in ccRCC patients.
- Overexpression of miR-1294 inhibited ccRCC cell proliferation, colony growth, and invasion.
- Homeobox A6 (HOXA6) was identified as a direct target of miR-1294 and negatively regulated by it.
Conclusions:
- miR-1294 functions as a tumor suppressor in ccRCC.
- Restoring miR-1294 levels can inhibit ccRCC cell proliferation, colony formation, and invasion.
- The tumor-suppressive role of miR-1294 is partially mediated through its regulation of HOXA6.
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