An iPSC Line from Human Pancreatic Ductal Adenocarcinoma Undergoes Early to Invasive Stages of Pancreatic Cancer Progression

被引:147
作者
Kim, Jungsun [1 ,2 ,3 ]
Hoffman, John P. [10 ]
Alpaugh, R. Katherine [11 ]
Rhim, Andrew D. [3 ,4 ,5 ]
Reichert, Maximilian [3 ,4 ,5 ]
Stanger, Ben Z. [3 ,4 ,5 ]
Furth, Emma E. [6 ]
Sepulveda, Antonia R. [6 ]
Yuan, Chao-Xing [7 ]
Won, Kyoung-Jae [8 ,9 ]
Donahue, Greg [1 ,2 ,3 ]
Sands, Jessica [1 ,2 ,3 ]
Gumbs, Andrew A. [10 ]
Zaret, Kenneth S. [1 ,2 ,3 ]
机构
[1] Univ Penn, Perelman Sch Med, Inst Regenerat Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Div Gastroenterol, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[7] Univ Penn, Perelman Sch Med, Prote Core Facil, Philadelphia, PA 19104 USA
[8] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[9] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[10] Fox Chase Canc Ctr, Dept Surg Oncol, Philadelphia, PA 19111 USA
[11] Fox Chase Canc Ctr, Protocol Support Lab, Philadelphia, PA 19111 USA
关键词
PLURIPOTENT STEM-CELLS; GENE-EXPRESSION; SELF-RENEWAL; TUMORS; CARCINOMA; MOUSE; BETA; MICE; DIFFERENTIATION; TRANSPLANTATION;
D O I
10.1016/j.celrep.2013.05.036
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) carries a dismal prognosis and lacks a human cell model of early disease progression. When human PDAC cells are injected into immunodeficient mice, they generate advanced-stage cancer. We hypothesized that if human PDAC cells were converted to pluripotency and then allowed to differentiate back into pancreatic tissue, they might undergo early stages of cancer. Although most induced pluripotent stem cell (iPSC) lines were not of the expected cancer genotype, one PDAC line, 10-22 cells, when injected into immunodeficient mice, generated pancreatic intraepithelial neoplasia (PanIN) precursors to PDAC that progressed to the invasive stage. The PanIN-like cells secrete or release proteins from many genes that are known to be expressed in human pancreatic cancer progression and that predicted an HNF4 alpha network in intermediate-stage lesions. Thus, rare events allow iPSC technology to provide a live human cell model of early pancreatic cancer and insights into disease progression.
引用
收藏
页码:2088 / 2099
页数:12
相关论文
共 49 条
[1]   Senescence impairs successful reprogramming to pluripotent stem cells [J].
Banito, Ana ;
Rashid, Sheikh T. ;
Acosta, Juan Carlos ;
Li, SiDe ;
Pereira, Carlos F. ;
Geti, Imbisaat ;
Pinho, Sandra ;
Silva, Jose C. ;
Azuara, Veronique ;
Walsh, Martin ;
Vallier, Ludovic ;
Gil, Jesus .
GENES & DEVELOPMENT, 2009, 23 (18) :2134-2139
[2]   Epigenetic Memory and Preferential Lineage-Specific Differentiation in Induced Pluripotent Stem Cells Derived from Human Pancreatic Islet Beta Cells [J].
Bar-Nur, Ori ;
Russ, Holger A. ;
Efrat, Shimon ;
Benvenisty, Nissim .
CELL STEM CELL, 2011, 9 (01) :17-23
[3]  
Blelloch RH, 2004, P NATL ACAD SCI USA, V101, P13985, DOI 10.1073/pnas.0405015101
[4]   Reference Maps of Human ES and iPS Cell Variation Enable High-Throughput Characterization of Pluripotent Cell Lines [J].
Bock, Christoph ;
Kiskinis, Evangelos ;
Verstappen, Griet ;
Gu, Hongcang ;
Boulting, Gabriella ;
Smith, Zachary D. ;
Ziller, Michael ;
Croft, Gist F. ;
Amoroso, Mackenzie W. ;
Oakley, Derek H. ;
Gnirke, Andreas ;
Eggan, Kevin ;
Meissner, Alexander .
CELL, 2011, 144 (03) :439-452
[5]   Progression of pancreatic intraductal neoplasias to infiltrating adenocarcinoma of the pancreas [J].
Brat, DJ ;
Lillemoe, KD ;
Yeo, CJ ;
Warfield, PB ;
Hruban, RH .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (02) :163-169
[6]   Transcriptome analysis of microdissected pancreatic intraepithelial neoplastic lesions [J].
Buchholz, M ;
Braun, M ;
Heidenblut, A ;
Kestler, HA ;
Klöppel, G ;
Schmiegel, W ;
Hahn, SA ;
Lüttges, J ;
Gress, TM .
ONCOGENE, 2005, 24 (44) :6626-6636
[7]   Generation of iPSCs from cultured human malignant cells [J].
Carette, Jan E. ;
Pruszak, Jan ;
Varadarajan, Malini ;
Blomen, Vincent A. ;
Gokhale, Sumita ;
Camargo, Fernando D. ;
Wernig, Marius ;
Jaenisch, Rudolf ;
Brummelkamp, Thijn R. .
BLOOD, 2010, 115 (20) :4039-4042
[8]   Modeling Pancreatic Cancer In Vivo From Xenograft and Carcinogen-Induced Systems to Genetically Engineered Mice [J].
Ding, Yongzeng ;
Cravero, John D. ;
Adrian, Kevin ;
Grippo, Paul .
PANCREAS, 2010, 39 (03) :283-292
[9]   A Complex Role for FGF-2 in Self-Renewal, Survival, and Adhesion of Human Embryonic Stem Cells [J].
Eiselleova, Livia ;
Matulka, Kamil ;
Kriz, Vitezslav ;
Kunova, Michaela ;
Schmidtova, Zuzana ;
Neradil, Jakub ;
Tichy, Boris ;
Dvorakova, Dana ;
Pospisilova, Sarka ;
Hampl, Ales ;
Dvorak, Petr .
STEM CELLS, 2009, 27 (08) :1847-1857
[10]   Cancer epigenomics: DNA methylomes and histone-modification maps [J].
Esteller, Manel .
NATURE REVIEWS GENETICS, 2007, 8 (04) :286-298