期刊
CELLULAR ONCOLOGY
卷 42, 期 6, 页码 769-781出版社
SPRINGER
DOI: 10.1007/s13402-019-00460-0
关键词
Hepatocellular carcinoma; Anoikis; Growth; Metastasis; PRDX4
资金
- Natural Science Foundation of Anhui Province [1708085QH177, 1808085MH234]
- National Natural Science Foundation of China [81201906]
- Chinese foundation for hepatitis prevention and control-TianQing liver disease research fund subject [TQGB20170171]
Purpose Peroxiredoxin 4 (PRDX4) has been reported to play a dual role in the progression of hepatocellular carcinoma (HCC). As yet, however, the underlying molecular mechanism has not been fully elucidated. Methods We examined the effects of PRDX4 on the growth and survival of HCC cells in an anchorage-independent microenvironment. The regulation of alpha-catenin stability and activity by PRDX4 was investigated. Results We found that PRDX4 depletion reduced, and PRDX4 overexpression increased, both anchorage-dependent and anchorage-independent growth of HCC cells. We also found that PRDX4 depletion caused an overproduction of reactive oxygen species (ROS) in HCC cells, especially under suspension conditions. PRDX4 knockdown predisposed HCC cells to anoikis, whereas PRDX4 overexpression induced resistance to anoikis. Subsequent in vivo studies confirmed that PRDX4 deficiency blocks HCC tumor growth and pulmonary metastasis. Mechanistically, we found that RDX4 reduced beta-TrCP-mediated beta-catenin ubiquitination and enhanced beta-catenin protein stability, consequently leading to activation of beta-catenin signaling. Silencing of beta-catenin impaired PRDX4-mediated anchorage-independent growth and survival, whereas beta-catenin overexpression increased the survival and growth of PRDX4-depleted cells under anchorage-independent conditions. Further investigation revealed that the beta-catenin downstream gene ID2 is responsible for the oncogenic activity of PRDX4 in HCC cells, promoting anchorage-independent growth and anoikis resistance. Conclusions PRDX4 reduces anoikis and promotes tumorigenesis and metastasis of HCC cells through stabilization of the beta-catenin protein and upregulation of ID2. Targeting of PRDX4 may represent a promising strategy to block HCC cell growth and metastasis.
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