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
相关论文
共 41 条
  • [11] MicroRNA-192 targeting retinoblastoma 1 inhibits cell proliferation and induces cell apoptosis in lung cancer cells
    Feng, Shipeng
    Cong, Shujie
    Zhang, Xin
    Bao, Xichen
    Wang, Wei
    Li, Huiping
    Wang, Zhe
    Wang, Guoxin
    Xu, Jianzhen
    Du, Bowen
    Qu, Dezhong
    Xiong, Wei
    Yin, Menghui
    Ren, Xiaoshuai
    Wang, Feifei
    He, Jianxing
    Zhang, Biliang
    [J]. NUCLEIC ACIDS RESEARCH, 2011, 39 (15) : 6669 - 6678
  • [12] MicroRNA-192 suppresses liver metastasis of colon cancer
    Geng, L.
    Chaudhuri, A.
    Talmon, G.
    Wisecarver, J. L.
    Are, C.
    Brattain, M.
    Wang, J.
    [J]. ONCOGENE, 2014, 33 (46) : 5332 - 5340
  • [13] Suppression of the uPAR-uPA System Retards Angiogenesis, Invasion, and In Vivo Tumor Development in Pancreatic Cancer Cells
    Gorantla, Bharathi
    Asuthkar, Swapna
    Rao, Jasti S.
    Patel, Jitendra
    Gondi, Christopher S.
    [J]. MOLECULAR CANCER RESEARCH, 2011, 9 (04) : 377 - 389
  • [14] Gutierrez LS, 2000, CANCER RES, V60, P5839
  • [15] The Silencing of MicroRNA 148a Production by DNA Hypermethylation Is an Early Event in Pancreatic Carcinogenesis
    Hanoun, Naima
    Delpu, Yannick
    Suriawinata, Arief A.
    Bournet, Barbara
    Bureau, Christophe
    Selves, Janick
    Tsongalis, Gregory J.
    Dufresne, Marlene
    Buscail, Louis
    Cordelier, Pierre
    Torrisani, Jerome
    [J]. CLINICAL CHEMISTRY, 2010, 56 (07) : 1107 - 1118
  • [16] Phase II randomised proof-of-concept study of the urokinase inhibitor upamostat (WX-671) in combination with gemcitabine compared with gemcitabine alone in patients with non-resectable, locally advanced pancreatic cancer
    Heinemann, V.
    Ebert, M. P.
    Laubender, R. P.
    Bevan, P.
    Mala, C.
    Boeck, S.
    [J]. BRITISH JOURNAL OF CANCER, 2013, 108 (04) : 766 - 770
  • [17] TUMOR-ASSOCIATED PROTEOLYSIS AND PROGNOSIS - NEW FUNCTIONAL RISK-FACTORS IN GASTRIC-CANCER DEFINED BY THE UROKINASE-TYPE PLASMINOGEN-ACTIVATOR SYSTEM
    HEISS, MM
    BABIC, R
    ALLGAYER, H
    GRUETZNER, KU
    JAUCH, KW
    LOEHRS, U
    SCHILDBERG, FW
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) : 2084 - 2093
  • [18] Clinical and Genetic Characteristics of Hereditary Pancreatitis in Europe
    Howes, Nathan
    Lerch, Markus M.
    Greenhalf, William
    Stocken, Deborah D.
    Ellis, Ian
    Simon, Peter
    Truninger, Kaspar
    Ammann, Rudi
    Cavallini, Giorgio
    Charnley, Richard M.
    Uomo, Generoso
    Delhaye, Miriam
    Spicak, Julius
    Drumm, Brendan
    Jansen, Jan
    Mountford, Roger
    Whitcomb, David C.
    Neoptolemos, John P.
    [J]. CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2004, 2 (03) : 252 - 261
  • [19] BMP-6 inhibits cell proliferation by targeting microRNA-192 in breast cancer
    Hu, Fen
    Meng, Xiangzhi
    Tong, Qi
    Liang, Lin
    Xiang, Rong
    Zhu, Tianhui
    Yang, Shuang
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2013, 1832 (12): : 2379 - 2390
  • [20] Mesenchymal stem cells regulate epithelial-mesenchymal transition and tumor progression of pancreatic cancer cells
    Kabashima-Niibe, Ayano
    Higuchi, Hajime
    Takaishi, Hiromasa
    Masugi, Yohei
    Matsuzaki, Yumi
    Mabuchi, Yo
    Funakoshi, Shinsuke
    Adachi, Masayuki
    Hamamoto, Yasuo
    Kawachi, Shigeyuki
    Aiura, Koichi
    Kitagawa, Yuko
    Sakamoto, Michiie
    Hibi, Toshifumi
    [J]. CANCER SCIENCE, 2013, 104 (02): : 157 - 164