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Updated: Feb 18, 2026

MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues
Published on: November 30, 2013
MiR-199a targeting ROCK1 to affect kidney cell proliferation, invasion and apoptosis
Zhigang Qin1, Xin Wei2, Ning Jin2
1a Department of Neurosurgery , China-Japan Union Hospital of Jilin University , Changchun , China.
Abstract:
Renal cell carcinoma (RCC) is one of the three most common cancers of urinary tract cancer, accounting for 2-3% of all systemic cancers. Recent studies have found that miR-199a is lowly expressed in RCC, may act as a tumour suppressor gene to induce the occurrence of kidney cancer. In the present study, we investigated the role of miR-199a in the progression and metastasis of RCC. The results showed that miR-199a significantly downregulated in RCC and cell lines. Overexpression of miR-199a in RCC cell lines significantly inhibited cell proliferation, migration and invasion. Furthermore, the qRT-PCR and western blot results showed that miR-199a overexpression significantly downregulated ROCK-1 mRNA and protein levels. ROCK1 was identified as a target of miR-199a, and ectopic expression of miR-199a downregulated ROCK1 by direct binding to its 3' untranslated region. Together, these findings indicate that miR-199a acts as a tumour suppressor and its downregulation in tumour tissues may contribute to the progression and metastasis of RCC through a mechanism involving ROCK1, suggesting miR-199a as a potential new diagnostic and therapeutic target for the treatment of RCC.
Insights
MicroRNA-199a (miR-199a) acts as a tumor suppressor in kidney cancer. Its low levels in renal cell carcinoma (RCC) correlate with progression, and restoring miR-199a inhibits cancer cell growth and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Renal cell carcinoma (RCC) accounts for 2-3% of systemic cancers.
- Recent studies suggest microRNA-199a (miR-199a) may function as a tumor suppressor in RCC.
- Low expression of miR-199a has been observed in RCC tissues.
Purpose of the Study:
- To investigate the role of miR-199a in the progression and metastasis of renal cell carcinoma.
- To determine the molecular mechanisms underlying miR-199a's function in RCC.
- To evaluate miR-199a as a potential diagnostic and therapeutic target for RCC.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess miR-199a and ROCK1 mRNA levels.
- Western blot analysis to evaluate ROCK1 protein expression.
- Cell culture experiments involving miR-199a overexpression in RCC cell lines to assess proliferation, migration, and invasion.
Main Results:
- miR-199a was significantly downregulated in RCC tissues and cell lines.
- Overexpression of miR-199a inhibited RCC cell proliferation, migration, and invasion.
- miR-199a directly targeted ROCK1, downregulating its mRNA and protein levels.
- ROCK1 was identified as a direct target of miR-199a through binding to its 3' untranslated region.
Conclusions:
- miR-199a functions as a tumor suppressor in renal cell carcinoma.
- Downregulation of miR-199a contributes to RCC progression and metastasis, potentially via ROCK1.
- miR-199a represents a promising novel diagnostic and therapeutic target for RCC treatment.
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