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Updated: Dec 30, 2025

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
MicroRNA-92b-3p is a prognostic oncomiR that targets TSC1 in clear cell renal cell carcinoma
Cong Wang1, Motohide Uemura1,2, Eisuke Tomiyama1
1Department of Urology, Osaka University Graduate School of Medicine, Suita, Japan.
Abstract:
Although several studies have reported that microRNA (miR)-92b-3p is involved in various cellular processes related to carcinogenesis, its physiological role in clear cell renal cell carcinoma (ccRCC) remains unclear. To clarify the role of miR-92b-3p in ccRCC, we compared miR-92b-3p expression levels in ccRCC tissues and adjacent normal renal tissues. Significant upregulation of miR-92b-3p was observed in ccRCC tissues. Overexpression of miR-92b-3p using a miRNA mimic promoted proliferation, migration, and invasion activities of ACHN cells. Functional inhibition of miR-92b-3p by a hairpin miRNA inhibitor suppressed Caki-2 cell growth and invasion activities in vitro. Mechanistically, it was found that miR-92b-3p directly targeted the TSC1 gene, a known upstream regulator of mTOR. Overexpression of miR-92b-3p decreased the protein expression of TSC1 and enhanced the downstream phosphorylation of p70S6 kinase, suggesting that the mTOR signaling pathway was activated by miR-92b-3p in RCC cells. Importantly, a multivariate Cox proportion hazard model, based on TNM staging and high levels of miR-92b-3p, revealed that miR-92b-3p expression (high vs. low hazard ratio, 2.86; 95% confidence interval, 1.20-6.83; P = .018) was a significant prognostic factor for overall survival of ccRCC patients with surgical management. Taken together, miR-92b-3p was found to act as an oncomiR, promoting cell proliferation by downregulating TSC1 in ccRCC.
Insights
MicroRNA (miR)-92b-3p is upregulated in clear cell renal cell carcinoma (ccRCC), promoting cancer cell proliferation and invasion. This oncomiR targets TSC1, activating the mTOR pathway and serving as a poor prognostic factor for ccRCC patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miR)-92b-3p is implicated in carcinogenesis, but its role in clear cell renal cell carcinoma (ccRCC) is not well understood.
- Understanding miR-92b-3p's function is crucial for developing targeted therapies for ccRCC.
Purpose of the Study:
- To investigate the role and mechanism of miR-92b-3p in ccRCC.
- To determine if miR-92b-3p expression correlates with patient prognosis.
Main Methods:
- Compared miR-92b-3p expression in ccRCC tissues and normal tissues.
- Utilized miRNA mimics and inhibitors to assess miR-92b-3p's functional impact on ccRCC cell lines (ACHN, Caki-2).
- Performed gene target analysis (TSC1) and pathway analysis (mTOR signaling).
- Conducted a multivariate Cox regression analysis for prognostic evaluation.
Main Results:
- miR-92b-3p was significantly upregulated in ccRCC tissues.
- Overexpression of miR-92b-3p enhanced ccRCC cell proliferation, migration, and invasion.
- Inhibition of miR-92b-3p suppressed ccRCC cell growth and invasion.
- miR-92b-3p directly targets TSC1, leading to decreased TSC1 protein and activated mTOR signaling.
- High miR-92b-3p expression is a significant negative prognostic factor for ccRCC patient survival.
Conclusions:
- miR-92b-3p acts as an oncomiR in ccRCC by downregulating TSC1 and promoting cell proliferation.
- miR-92b-3p is a potential therapeutic target and prognostic biomarker for ccRCC.
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