4.8 Article

Early Epigenetic Downregulation of microRNA-192 Expression Promotes Pancreatic Cancer Progression

Journal

CANCER RESEARCH
Volume 76, Issue 14, Pages 4149-4159

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-15-0390

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Funding

  1. Cancer Research UK [8968] Funding Source: Medline
  2. Pancreatic Cancer UK [RIF2014_03_COSTELLO] Funding Source: Medline
  3. Cancer Research UK [15957, 8968, 16812] Funding Source: researchfish
  4. National Institute for Health Research [NF-SI-0510-10126] Funding Source: researchfish

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Pancreatic ductal adenocarcinoma (PDAC) is characterized by very early metastasis, suggesting the hypothesis that metastasis-associated changes may occur prior to actual tumor formation. In this study, we identified miR-192 as an epigenetically regulated suppressor gene with predictive value in this disease. miR-192 was downregulated by promoter methylation in both PDAC and chronic pancreatitis, the latter of which is a major risk factor for the development of PDAC. Functional studies in vitro and in vivo in mouse models of PDAC showed that overexpression of miR-192 was sufficient to reduce cell proliferation and invasion. Mechanistic analyses correlated changes in miR-192 promoter methylation and expression with epithelial-mesenchymal transition. Cell proliferation and invasion were linked to altered expression of the miR-192 target gene SERPINE1 that is encoding the protein plasminogen activator inhibitor-1 (PAI-1), an established regulator of these properties in PDAC cells. Notably, our data suggested that invasive capacity was altered even before neoplastic transformation occurred, as triggered by miR-192 downregulation. Overall, our results highlighted a role for miR-192 in explaining the early metastatic behavior of PDAC and suggested its relevance as a target to develop for early diagnostics and therapy. (C)2016 AACR.

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