Abstract
The liver transplant (LT) situation represents an attractive model for studying hepatocellular carcinoma (HCC) metastasis. Based on microarray data, we previously found that miR-126 expression was lower in tumor tissues of patients with post-LT HCC recurrence compared with non-recurrence. In this study, we examined the expression of miR-126 in HCC samples from 68 patients who had undergone LT using quantitative real-time PCR and analyzed its correlation with clinicopathological features and prognosis of patients. Furthermore, we performed experimental analyses to explore the involvement of miR-126 in HCC metastasis. We found that miR-126 levels were lower in tumor tissues of patients with post-LT HCC recurrence in comparison to patients with no-recurrence (p = 0.009). Lower expression of miR-126 in HCC was associated significantly with tumor recurrence (p = 0.011) and poor survival (p = 0.009) of patients. Functional studies indicated that ectopic expression of miR-126 significantly inhibits HCC cells migration, invasion, proliferation and colony formation in vitro, and suppresses experimental lung colonization in vivo. Our study revealed that down-regulation of miR-126 plays an important role in HCC metastasis, and suggest a potential application of miR-126 in prognosis prediction and HCC treatment.
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Abbreviations
- HCC:
-
Hepatocellular carcinoma
- LT:
-
Liver transplant
- miR(s):
-
MicroRNA(s)
- qRT-PCR:
-
Quantitative real time-polymerase chain reaction
- FFPE:
-
Formalin-fixed paraffin embedded
- MET:
-
Mesenchymal epithelial transition
- OS:
-
Overall survival
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Acknowledgments
This study was supported by National Key Technology R&D Program (2008BAI60B03).
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The authors disclosed no commercial or financial interest in the subject of study.
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H. Chen, R. Miao and J. Fan contributed equally to this study.
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Chen, H., Miao, R., Fan, J. et al. Decreased expression of miR-126 correlates with metastatic recurrence of hepatocellular carcinoma. Clin Exp Metastasis 30, 651–658 (2013). https://doi.org/10.1007/s10585-013-9569-6
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DOI: https://doi.org/10.1007/s10585-013-9569-6