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A Huaier polysaccharide reduced metastasis of human hepatocellular carcinoma SMMC-7721 cells via modulating AUF-1 signaling pathway

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Tumor Biology

Abstract

TP-1 is a polysaccharide from one famous fungus Huaier. Treatment with TP-1 significantly inhibited the cell growth, adhesion, migration, and motility of SMMC-7721 cells in a dose-dependent manner. Real-time quantitative RT-PCR revealed a dose-dependent decrease in RNA-binding factor 1 (AUF-1) and astrocyte elevated gene-1 (AEG-1) messenger RNA (mRNA) levels in TP-1-treated SMMC-7721 cells, which is consistent with their protein expression detected by Western blotting. On the contrary, microRNA-122 (miR-122) expression increased in SMMC-7721 cells following TP-1 treatment. Moreover, TP-1 treatment at three doses apparently increased epithelial marker E-cadherin protein expression but decreased the mesenchymal marker N-cadherin protein level. In addition, the hematoxylin-eosin (H & E) staining showed that the TP-1 significantly inhibited the lung metastasis of liver cancer in mice orthotopic implanted with SMMC-7721 tumor tissue. Taken together, these findings proved the inhibitory effect of TP-1 on the growth and metastasis of SMMC-7721 cells, and TP-1 might be offered for future application as a powerful chemopreventive agent against hepatocellular carcinoma (HCC) metastasis.

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Acknowledgments

This research is funded by the National Natural Science Foundation of China (grant no. 81472328); Liver Disease AIDS Foundation of You An Hospital, Capital Medical University (BJYAH-2011-034); National Science and Technology Support Project (2012BAI15B08); and Key Project of National Communicable Disease (2012ZX10002015-002).

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The authors declare that they have no conflicts of interest concerning this article.

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Correspondence to Jiasheng Zheng.

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Cong Li and Xia Wu contributed equally to this work.

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Li, C., Wu, X., Zhang, H. et al. A Huaier polysaccharide reduced metastasis of human hepatocellular carcinoma SMMC-7721 cells via modulating AUF-1 signaling pathway. Tumor Biol. 36, 6285–6293 (2015). https://doi.org/10.1007/s13277-015-3314-5

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  • DOI: https://doi.org/10.1007/s13277-015-3314-5

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