ETS-Transcription Factor ETV1 Regulates Stromal Expansion and Metastasis in Pancreatic Cancer

被引:51
|
作者
Heeg, Steffen [1 ,2 ,3 ,4 ]
Das, Koushik K. [1 ,2 ,3 ]
Reichert, Maximilian [1 ,2 ,3 ,5 ]
Bakir, Basil [1 ,2 ,3 ]
Takano, Shigetsugu [1 ,2 ,3 ]
Caspers, Julia [4 ]
Aiello, Nicole M. [1 ,2 ,3 ]
Wu, Katherine [1 ]
Neesse, Albrecht [6 ]
Maitra, Anirban [7 ]
Iacobuzio-Donahue, Christine A. [8 ]
Hicks, Philip [1 ,2 ,3 ]
Rustgi, Anil K. [1 ,2 ,3 ,9 ]
机构
[1] Univ Penn, Div Gastroenterol, Perelman Sch Med, 900 Biomed Res Bldg 2-3,415 Curie Blvd, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[4] Univ Freiberg, Med Ctr, Dept Med 2, Freiburg, Germany
[5] Tech Univ Munich, Med Klin 2, Munich, Germany
[6] Univ Med Ctr Goettingen, Div Gastroenterol & Gastrointestinal Oncol, Gottingen, Germany
[7] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Mem Sloan Kettering Canc Ctr, David M Rubenstein Ctr Pancreat Canc Res, 1275 York Ave, New York, NY 10021 USA
[9] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
关键词
EMT; Pancreas; Cancer; Gene Regulation; TO-MESENCHYMAL TRANSITION; DUCTAL ADENOCARCINOMA; GENE-EXPRESSION; CELLS; REGENERATION; DESMOPLASIA; SURVIVAL; DISTINCT; LINEAGE;
D O I
10.1053/j.gastro.2016.06.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: The ETS-transcription factor ETV1 is involved in epithelial-mesenchymal transition during pancreatic development and is induced in mouse pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal adenocarcinoma (PDAC). We investigated the function of ETV1 in stromal expansion of PDAC and metastasis, as well as its effects on a novel downstream target Sparc, which encodes a matricellular protein found in PDAC stroma that has been associated with invasiveness, metastasis and poor patient outcomes. METHODS: Pancreatic ductal cells were isolated from Pdx1Cre; Kras(G12D/+) mice (PanIN), Pdx1Cre; Kras(G12D/+); p53(fl/+) and Pdx1Cre; Kras(G12D/+); p53(fl/+); Rosa26(YFP) mice (PDAC), and Pdx1Cre; Kras(G12D/+); p53(fl/+); Sparc(-/-) mice. Cells were grown in 3-dimensional organoid culture to analyze morphology, proliferation, and invasion. Human PanIN and PDAC tissues were evaluated for ETV1 expression. Orthotopic pancreatic transplants of ETV1-overexpressing PDAC and respective control cells were performed. RESULTS: ETV1 expression was significantly increased in human PanINs and, even more so, in primary and metastatic PDAC. Analyses of mouse orthotopic xenografts revealed that ETV1 induced significantly larger primary tumors than controls, with significantly increased stromal expansion, ascites and metastases. In 3-dimensional organoids, ETV1 disrupted cyst architecture, induced EMT, and increased invasive capacity. Furthermore, we identified Sparc as a novel functional gene target of Etv1 by luciferase assays, and SPARC and ETV1 proteins co-localized in vivo. Disruption of Sparc abrogates the phenotype of stromal expansion and metastasis found with ETV1 overexpression in vivo. We identified hyaluronan synthase 2 (Has2) as another novel downstream factor of Etv1; that may mediate ETV1's significant expansion of hyaluronic acid in PDAC stroma. Conversely, disruption of Etv1 in PDAC mice (Pdx1Cre; Kras(G12D/+); p53(fl/+); Rosa26(YFP); Cre; Etv1(fl/fl)) reduced levels of SPARC and hyaluronic acid in the stroma. CONCLUSIONS: ETV1 is critical in the desmoplastic stromal expansion and metastatic progression of pancreatic cancer in mice, mediated functionally in part through Sparc and Has2.
引用
收藏
页码:540 / +
页数:28
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