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Updated: May 4, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
RETRACTED: miRNA-302b suppresses human hepatocellular carcinoma by targeting AKT2
Lumin Wang1, Jiayi Yao, Xiaogang Zhang
1Department of Genetics and Molecular Biology, Xi'an Jiaotong, University School of Medicine, 76 Yan Ta West Road, Xi'an, Shaanxi 710061, China. hchen@mail.xjtu.edu.cn.
Unlabelled:
miRNAs (miR) play a critical role in human cancers, including hepatocellular carcinoma. Although miR-302b has been suggested to function as a tumor repressor in other cancers, its role in hepatocellular carcinoma is unknown. This study investigated the expression and functional role of miR-302b in human hepatocellular carcinoma. The expression level of miR-302b is dramatically decreased in clinical hepatocellular carcinoma specimens, as compared with their respective nonneoplastic counterparts, and in hepatocellular carcinoma cell lines. Overexpression of miR-302b suppressed hepatocellular carcinoma cell proliferation and G1-S transition in vitro, whereas inhibition of miR-302b promoted hepatocellular carcinoma cell proliferation and G1-S transition. Using a luciferase reporter assay, AKT2 was determined to be a direct target of miR-302b. Subsequent investigation revealed that miR-302b expression was inversely correlated with AKT2 expression in hepatocellular carcinoma tissue samples. Importantly, silencing AKT2 recapitulated the cellular and molecular effects seen upon miR-302b overexpression, which included inhibiting hepatocellular carcinoma cell proliferation, suppressing G1 regulators (Cyclin A, Cyclin D1, CDK2) and increasing p27Kip1 phosphorylation at Ser10. Restoration of AKT2 counteracted the effects of miR-302b expression. Moreover, miR-302b was able to repress tumor growth of hepatocellular carcinoma cells in vivo.
Implications:
Taken together, miR-302b inhibits HCC cell proliferation and growth in vitro and in vivo by targeting AKT2.
Insights
MicroRNA-302b (miR-302b) acts as a tumor suppressor in hepatocellular carcinoma (HCC). This study found miR-302b inhibits HCC cell proliferation and growth by targeting AKT2.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are crucial in human cancers.
- The role of miR-302b in hepatocellular carcinoma (HCC) was previously unknown.
- miR-302b is a potential tumor suppressor in various cancers.
Purpose of the Study:
- To investigate the expression and function of miR-302b in HCC.
- To identify the molecular targets of miR-302b in HCC.
- To determine the therapeutic potential of miR-302b in HCC.
Main Methods:
- Quantitative real-time PCR to assess miR-302b expression.
- In vitro cell proliferation and cell cycle assays.
- Luciferase reporter assays to identify direct targets.
- Western blotting to analyze protein expression.
- In vivo tumor xenograft models.
Main Results:
- miR-302b expression was significantly downregulated in HCC tissues and cell lines.
- Overexpression of miR-302b suppressed HCC cell proliferation and G1-S transition.
- AKT2 was identified as a direct target of miR-302b.
- Silencing AKT2 mimicked the tumor-suppressive effects of miR-302b.
- miR-302b repressed HCC tumor growth in vivo.
Conclusions:
- miR-302b functions as a tumor suppressor in hepatocellular carcinoma.
- miR-302b inhibits HCC cell proliferation and growth by targeting AKT2.
- miR-302b holds potential as a therapeutic agent for HCC.
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