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Updated: May 10, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
The novel gene MIA2 acts as a tumour suppressor in hepatocellular carcinoma
C Hellerbrand1, T Amann, J Schlegel
1University of Regensburg, Department of Internal Medicine I, D-93042 Regensburg, Germany. claus.hellerbrand@klinik.uni-regensburg.de
Background:
Melanoma inhibitory activity 2 (MIA2) is a novel gene of the MIA gene family. The selective expression of MIA2 in hepatocytes is controlled by hepatocyte nuclear factor (HNF) 1 binding sites in the MIA2 promotor. In contrast, in most hepatocellular carcinomas (HCC) MIA2 expression is down-regulated or lost.
Aim:
In this study we examined the regulation and functional role of MIA2 in hepatocancerogenesis.
Methods And Results:
In HCC cell lines and tissues HNF-1 expression was lower than in primary human hepatocytes (PHH) and corresponding non-tumorous tissue, respectively, and correlated significantly with the down-regulation of MIA2 expression. Re-expression of HNF-1 in HCC cells reinduced MIA2 in HCC cells to similar levels as found in PHH. Further, MIA2 was re-expressed in HCC cell lines by stable transfection, and the generated cell clones revealed a strongly reduced invasive potential and proliferation rate in vitro. In line with these findings treatment of HCC cells with recombinant MIA2 inhibited proliferation and invasion. In nude mice MIA2 re-expressing HCC cells grew significantly slower and revealed a less invasive growth pattern. Immunohistochemical analysis of a tissue microarray containing HCC and corresponding non-cancerous liver tissue of 85 patients confirmed reduced MIA2 expression in HCC. Furthermore, MIA2 negative HCC tissue showed a significantly higher Ki67 labelling index and loss of MIA2 expression correlated significantly with more advanced tumour stages.
Conclusion:
This study presents MIA2 as an inhibitor of HCC growth and invasion both in vitro and in vivo, and consequently, as a tumour suppressor of HCC. Further, our findings indicate a novel mechanism, how loss of HNF-1 expression in HCC affects tumorigenicity via down-regulation of MIA2.
Insights
Melanoma inhibitory activity 2 (MIA2) acts as a tumor suppressor in hepatocellular carcinoma (HCC). Loss of MIA2, linked to HNF-1 down-regulation, promotes HCC growth and invasion.
Area of Science:
- Hepatocellular Carcinoma Research
- Molecular Biology
- Cancer Genetics
Background:
- Melanoma inhibitory activity 2 (MIA2) is selectively expressed in hepatocytes, regulated by hepatocyte nuclear factor (HNF) 1.
- MIA2 expression is often reduced or lost in hepatocellular carcinoma (HCC).
Purpose of the Study:
- To investigate the regulation and function of MIA2 in liver cancer development.
- To explore the role of HNF-1 in MIA2 expression and its impact on HCC.
Main Methods:
- Compared HNF-1 and MIA2 expression in HCC cell lines/tissues versus primary human hepatocytes (PHH).
- Re-expressed HNF-1 and MIA2 in HCC cells and assessed proliferation and invasion in vitro and in vivo.
- Analyzed MIA2 expression, Ki67 index, and tumor stage in 85 HCC patient samples.
Main Results:
- HNF-1 and MIA2 expression were lower in HCC compared to normal liver tissue.
- Restoring HNF-1 or MIA2 expression reduced HCC cell proliferation and invasion.
- Loss of MIA2 correlated with increased proliferation (Ki67) and advanced tumor stage in HCC patients.
Conclusions:
- MIA2 functions as a tumor suppressor, inhibiting HCC growth and invasion.
- Down-regulation of MIA2 due to HNF-1 loss is a mechanism contributing to HCC tumorigenicity.
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