BLIMP1 Induces Transient Metastatic Heterogeneity in Pancreatic Cancer

被引:54
作者
Chiou, Shin-Heng [1 ]
Risca, Viviana I. [1 ]
Wang, Gordon X. [2 ]
Yang, Dian [1 ,3 ]
Gruner, Barbara M. [1 ]
Kathiria, Arwa S. [1 ]
Ma, Rosanna K. [1 ]
Vaka, Dedeepya [1 ]
Chu, Pauline [4 ]
Kozak, Margaret [5 ]
Castellini, Laura [6 ]
Graves, Edward E. [3 ,6 ]
Kim, Grace E. [7 ]
Mourrain, Philippe [2 ]
Koong, Albert C. [3 ,5 ,6 ]
Giaccia, Amato J. [3 ,5 ,6 ]
Winslow, Monte M. [1 ,3 ,4 ,5 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Canc Biol Program, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Stanford Canc Inst, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Radiat Oncol, Sch Med, Stanford, CA 94305 USA
[7] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
关键词
PLASMA-CELL DIFFERENTIATION; TO-MESENCHYMAL TRANSITION; TUMOR-INITIATING CELLS; LYMPH-NODE METASTASIS; MOBILITY GROUP A2; STEM-CELLS; DUCTAL ADENOCARCINOMA; LUNG-CANCER; PROMOTES METASTASIS; DISTANT METASTASIS;
D O I
10.1158/2159-8290.CD-17-0250
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the most metastatic and deadly cancers. Despite the clinical signifi cance of metastatic spread, our understanding of molecular mechanisms that drive PDAC metastatic ability remains limited. By generating a genetically engineered mouse model of human PDAC, we uncover a transient subpopulation of cancer cells with exceptionally high metastatic ability. Global gene expression profi ling and functional analyses uncovered the transcription factor BLIMP1 as a driver of PDAC metastasis. The highly metastatic PDAC subpopulation is enriched for hypoxia-induced genes, and hypoxia-mediated induction of BLIMP1 contributes to the regulation of a subset of hypoxia-associated gene expression programs. These fi ndings support a model in which upregulation of BLIMP1 links microenvironmental cues to a metastatic stem cell character. SIGNIFICANCE: PDAC is an almost uniformly lethal cancer, largely due to its tendency for metastasis. We defi ne a highly metastatic subpopulation of cancer cells, uncover a key transcriptional regulator of metastatic ability, and defi ne hypoxia as an important factor within the tumor microenvironment that increases metastatic proclivity. (C) 2017 AACR.
引用
收藏
页码:1184 / 1199
页数:16
相关论文
共 82 条
[1]   An increased high-mobility group A2 expression level is associated with malignant phenotype in pancreatic exocrine tissue [J].
Abe, N ;
Watanabe, T ;
Suzuki, Y ;
Matsumoto, N ;
Masaki, T ;
Mori, T ;
Sugiyama, M ;
Chiappetta, G ;
Fusco, A ;
Atomi, Y .
BRITISH JOURNAL OF CANCER, 2003, 89 (11) :2104-2109
[2]   Activated Kras and Ink4a/Arf deficiency cooperate to produce metastatic pancreatic ductal adenocarcinoma [J].
Aguirre, AJ ;
Bardeesy, N ;
Sinha, M ;
Lopez, L ;
Tuveson, DA ;
Horner, J ;
Redston, MS ;
DePinho, RA .
GENES & DEVELOPMENT, 2003, 17 (24) :3112-3126
[3]   Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells [J].
Ancelin, Katia ;
Lange, Ulrike C. ;
Hajkova, Petra ;
Schneider, Robert ;
Bannister, Andrew J. ;
Kouzarides, Tony ;
Surani, M. Azim .
NATURE CELL BIOLOGY, 2006, 8 (06) :623-630
[4]   YVEGF-Mediated Induction of PRD1-BF1/Blimp1 Expression Sensitizes Tumor Vasculature to Oncolytic Virus Infection [J].
Arulanandam, Rozanne ;
Batenchuk, Cory ;
Angarita, Fernando A. ;
Ottolino-Perry, Kathryn ;
Cousineau, Sophie ;
Mottashed, Amelia ;
Burgess, Emma ;
Falls, Theresa J. ;
De Silva, Naomi ;
Tsang, Jovian ;
Howe, Grant A. ;
Bourgeois-Daigneault, Marie-Claude ;
Conrad, David P. ;
Daneshmand, Manijeh ;
Breitbach, Caroline J. ;
Kim, David H. ;
Raptis, Leda ;
Sad, Subash ;
Atkins, Harold ;
Huh, Michael S. ;
Diallo, Jean-Simon ;
Lichty, Brian D. ;
Ilkow, Carolina S. ;
Le Boeuf, Fabrice ;
Addison, Christina L. ;
McCart, J. Andrea ;
Bell, John C. .
CANCER CELL, 2015, 28 (02) :210-224
[5]   CD133+ Tumor Initiating Cells in a Syngenic Murine Model of Pancreatic Cancer Respond to Minnelide [J].
Banerjee, Sulagna ;
Nomura, Alice ;
Sangwan, Veena ;
Chugh, Rohit ;
Dudeja, Vikas ;
Vickers, Selwyn M. ;
Saluja, Ashok .
CLINICAL CANCER RESEARCH, 2014, 20 (09) :2388-2399
[6]   Both p16Ink4a and the p19Arf-p53 pathway constrain progression of pancreatic adenocarcinoma in the mouse [J].
Bardeesy, N ;
Aguirre, AJ ;
Chu, GC ;
Cheng, KH ;
Lopez, LV ;
Hezel, AF ;
Feng, B ;
Brennan, C ;
Weissleder, R ;
Mahmood, U ;
Hanahan, D ;
Redston, MS ;
Chin, L ;
DePinho, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5947-5952
[7]   Smad4 is dispensable for normal pancreas development yet critical in progression and tumor biology of pancreas cancer [J].
Bardeesy, Nabeel ;
Cheng, Kuang-hung ;
Berger, Justin H. ;
Chu, Gerald C. ;
Pahler, Jessica ;
Olson, Peter ;
Hezel, Aram F. ;
Horner, James ;
Lauwers, Gregory Y. ;
Hanahan, Douglas ;
DePinho, Ronald A. .
GENES & DEVELOPMENT, 2006, 20 (22) :3130-3146
[8]   HYPOXIA AND METABOLISM SERIES - TIMELINE The impact of O2 availability on human cancer [J].
Bertout, Jessica A. ;
Patel, Shetal A. ;
Simon, M. Celeste .
NATURE REVIEWS CANCER, 2008, 8 (12) :967-975
[9]  
Buenrostro JD, 2013, NAT METHODS, V10, P1213, DOI [10.1038/NMETH.2688, 10.1038/nmeth.2688]
[10]   Differential effects of physiologically relevant hypoxic conditions on T lymphocyte development and effector functions [J].
Caldwell, CC ;
Kojima, H ;
Lukashev, D ;
Armstrong, J ;
Farber, M ;
Apasov, SG ;
Sitkovsky, MV .
JOURNAL OF IMMUNOLOGY, 2001, 167 (11) :6140-6149