4.8 Article

Chromatin remodeling factor ARID2 suppresses hepatocellular carcinoma metastasis via DNMT1-Snail axis

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1914937117

关键词

hepatocellular carcinoma; metastases; epigenetic modification; methylation; mutations

资金

  1. National Key R&D Program of China [2018YFC1604404, 2018YFC1603002]
  2. Personalized Medicines-Molecular Signature-based Drug Discovery and Development, Strategic Priority Research Program of the Chinese Academy of Sciences [XDA12010316]
  3. National Natural Science Foundation of China [31520103907, 81730083, 31771538, 81972757]
  4. Youth Innovation Promotion Association of Chinese Academy of Sciences fund
  5. Sanofi-SIBS 2018 Young Faculty Award
  6. Postdoctoral Science Foundation of China [2017M622677]

向作者/读者索取更多资源

Recurrence and metastasis remain the major obstacles to successful treatment of hepatocellular carcinoma (HCC). Chromatin remodeling factor ARID2 is commonly mutated in HCC, indicating its important role in cancer development. However, its role in HCC metastasis is largely elusive. In this study, we find that ARID2 expression is significantly decreased in metastatic HCC tissues, showing negative correlation with pathological grade, organ metastasis and positive association with survival of HCC patients. ARID2 inhibits migration and invasion of HCC cells in vitro and metastasis in vivo. Moreover, ARID2 knockout promotes pulmonary metastasis in different HCC mouse models. Mechanistic study reveals that ARID2 represses epithelial-mesenchymal transition (EMT) of HCC cells by recruiting DNMT1 to Snail promoter, which increases promoter methylation and inhibits Snail transcription. In addition, we discover that ARID2 mutants with disrupted C2H2 domain lose the metastasis suppressor function, exhibiting a positive association with HCC metastasis and poor prognosis. In conclusion, our study reveals the metastasis suppressor role as well as the underlying mechanism of ARID2 in HCC and provides a potential therapeutic target for ARID2-deficient HCC.

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