Cellular Physiology and Biochemistry (Jul 2016)

NEDD4 Depletion Inhibits Hepatocellular Carcinoma Growth via Targeting PTEN

  • Xiaofeng Hang,
  • Shanbang Zhu,
  • Hongwei Di,
  • Zhiqin Wu,
  • Kaijian Chu,
  • Junxue Wang,
  • Haiguang Xin,
  • Guanzhen Yu,
  • Haoran Peng,
  • Xiaohui Miao,
  • Wensheng Xu

DOI
https://doi.org/10.1159/000445667
Journal volume & issue
Vol. 39, no. 2
pp. 768 – 779

Abstract

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Background/Aims: Neural precursor cell-expressed developmentally down-regulated gene 4 (NEDD4) plays an important role in tumor cell growth, yet its role in hepatocellular carcinoma (HCC) remains unclear. This study is to establish NEDD4 as a prognostic biomarker by which the survival of HCC patients can be predicted and to reveal the role of NEDD4 in hepatocellular carcinoma cell growth. Methods: The expression of NEDD4 in 219 HCC specimens was assessed by immunohistochemistry. Postoperative overall survival and time to recurrence were evaluated by univariate and multivariate analyses. The roles of NEDD4 in hepatocellular carcinoma cell proliferation and invasion were determined. Results: The patients with low NEDD4 expression tumors had an average cumulative survival of 64.9 ± 6.5 months during follow-up while the patients with high NEDD4 expression tumors had an average cumulative survival of 20.3 ± 15.8 months. NEDD4 silencing inhibited Huh7 cell proliferation and altered cell cytoskeletal assembly, and NEDD4 depletion furthermore seemed to suppress cell migration and invasion. A possible molecular mechanism for the observed effects might be that NEDD4 silence led to an increase in PTEN (phosphatase and tensin homologue) expression, which in turn resulted in the inactivation of STAT3, AKT, and ERK1/2. Conclusion: Our findings indicate that NEDD4 may participate in the HCC progression and may therefore be a potential target for HCC therapy.

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