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

被引:71
作者
Botla, Sandeep K. [1 ]
Savant, Soniya [2 ,3 ]
Jandaghi, Pouria [1 ]
Bauer, Andrea S. [1 ]
Muecke, Oliver [4 ]
Moskalev, Evgeny A. [5 ]
Neoptolemos, John P. [6 ]
Costello, Eithne [6 ]
Greenhalf, William [6 ]
Scarpa, Aldo [7 ]
Gaida, Matthias M. [8 ]
Buechler, Markus W. [9 ]
Strobel, Oliver [9 ]
Hackert, Thilo [9 ]
Giese, Nathalia A. [9 ]
Augustin, Hellmut G. [2 ,3 ,10 ]
Hoheisel, Joerg D. [1 ]
机构
[1] German Canc Res Ctr, Div Funct Genome Anal, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Div Vasc Oncol & Metastasis, D-69120 Heidelberg, Germany
[3] Heidelberg Univ, Dept Vasc Biol & Tumor Angiogenesis CBTM, Med Faulty Mannheim, Mannheim, Germany
[4] German Canc Res Ctr, Div Epigen & Canc Risk Factors, D-69120 Heidelberg, Germany
[5] Univ Erlangen Nurnberg, Diagnost Mol Pathol, Inst Pathol, Erlangen, Germany
[6] Natl Inst Hlth Res, Liverpool Pancreas Biomed Res Unit, Liverpool, Merseyside, England
[7] Univ Verona, Dept Pathol & Diagnost, Verona, Italy
[8] Univ Heidelberg Hosp, Dept Pathol, Heidelberg, Germany
[9] Univ Heidelberg Hosp, Dept Surg, Heidelberg, Germany
[10] German Canc Consortium, Heidelberg, Germany
关键词
PLASMINOGEN-ACTIVATOR INHIBITOR-1; EPITHELIAL-MESENCHYMAL TRANSITION; CELL-PROLIFERATION; DNA METHYLATION; OVARIAN-CANCER; E-CADHERIN; METASTASIS; BIOMARKERS; PROGNOSIS; MECHANISM;
D O I
10.1158/0008-5472.CAN-15-0390
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:4149 / 4159
页数:11
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