A new transgenic mouse model for conditional overexpression of the Polycomb Group protein EZH2

被引:9
作者
Koppens, Martijn A. J. [1 ]
Tanger, Ellen [1 ]
Nacerddine, Karim [1 ]
Westerman, Bart [1 ]
Song, Ji-Ying [2 ]
van Lohuizen, Maarten [1 ,3 ,4 ]
机构
[1] Netherlands Canc Inst, Div Mol Genet, H4012,Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Dept Expt Anim Pathol, Amsterdam, Netherlands
[3] Canc Genom Ctr Netherlands CGC nl, Utrecht, Netherlands
[4] Postbus 90203, NL-1006 BE Amsterdam, Netherlands
关键词
EZH2; Prostate cancer; Mouse model; Polycomb; PROSTATE-CANCER CELLS; ANDROGEN-RECEPTOR; GENE-EXPRESSION; HISTONE DEACETYLASE; LUNG-CANCER; MUTATIONS; TRANSFORMATION; METHYLATION; LYMPHOMAS; MELANOMA;
D O I
10.1007/s11248-016-9993-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Polycomb Group protein EZH2 is upregulated in most prostate cancers, and its overexpression is associated with poor prognosis. Most insights into the functional role of EZH2 in prostate cancer have been gained using cell lines and EZH2 inactivation studies. However, the question remains whether overexpression of EZH2 can initiate prostate tumourigenesis or drive tumour progression. Appropriate transgenic mouse models that are required to answer such questions are lacking. We developed one such transgenic mouse model for conditional overexpression of Ezh2. In this transgene, Ezh2 and Luciferase are transcribed from a single open reading frame. The latter gene enables intravital bioluminescent imaging of tissues expressing this transgene, allowing the detection of tumour outgrowth and potential metastatic progression over time. Prostate-specific Ezh2 overexpression by crossbreeding with Probasin-Cre mice led to neoplastic prostate lesions at low incidence and with a long latency. Compounding a previously described Bmi1-transgene and Pten-deficiency prostate cancer mouse model with the Ezh2 transgene did not enhance tumour progression or drive metastasis formation. In conclusion, we here report the generation of a wildtype Ezh2 overexpression mouse model that allows for intravital surveillance of tissues with activated transgene. This model will be an invaluable tool for further unravelling the role of EZH2 in cancer.
引用
收藏
页码:187 / 196
页数:10
相关论文
共 37 条
[1]   The role of histone deacetylases in prostate cancer [J].
Abbas, Ata ;
Gupta, Sanjay .
EPIGENETICS, 2008, 3 (06) :300-309
[2]   An IKKα-E2F1-BMI1 cascade activated by infiltrating B cells controls prostate regeneration and tumor recurrence [J].
Ammirante, Massimo ;
Kuraishy, Ali I. ;
Shalapour, Shabnam ;
Strasner, Amy ;
Ramirez-Sanchez, Claudia ;
Zhang, Weizhou ;
Shabaik, Ahmed ;
Karin, Michael .
GENES & DEVELOPMENT, 2013, 27 (13) :1435-1440
[3]   Epigenetic reprogramming by tumor-derived EZH2 gain-of-function mutations promotes aggressive 3D cell morphologies and enhances melanoma tumor growth [J].
Barsotti, Anthony M. ;
Ryskin, Michael ;
Zhong, Wenyan ;
Zhang, Wei-Guo ;
Giannakou, Andreas ;
Loreth, Christine ;
Diesl, Veronica ;
Follettie, Maximillian ;
Golas, Jonathon ;
Lee, Michelle ;
Nichols, Timothy ;
Fan, Conglin ;
Li, Gang ;
Dann, Stephen ;
Fantin, Valeria R. ;
Arndt, Kim ;
Verhelle, Dominique ;
Rollins, Robert A. .
ONCOTARGET, 2015, 6 (05) :2928-2938
[4]   EZH2 Is Required for Germinal Center Formation and Somatic EZH2 Mutations Promote Lymphoid Transformation [J].
Beguelin, Wendy ;
Popovic, Relja ;
Teater, Matt ;
Jiang, Yanwen ;
Bunting, Karen L. ;
Rosen, Monica ;
Shen, Hao ;
Yang, Shao Ning ;
Wang, Ling ;
Ezponda, Teresa ;
Martinez-Garcia, Eva ;
Zhang, Haikuo ;
Zheng, Yupeng ;
Verma, Sharad K. ;
McCabe, Michael T. ;
Ott, Heidi M. ;
Van Aller, Glenn S. ;
Kruger, Ryan G. ;
Liu, Yan ;
McHugh, Charles F. ;
Scott, David W. ;
Chung, Young Rock ;
Kelleher, Neil ;
Shaknovich, Rita ;
Creasy, Caretha L. ;
Gascoyne, Randy D. ;
Wong, Kwok-Kin ;
Cerchietti, Leandro ;
Levine, Ross L. ;
Abdel-Wahab, Omar ;
Licht, Jonathan D. ;
Elemento, Olivier ;
Melnick, Ari M. .
CANCER CELL, 2013, 23 (05) :677-692
[5]  
Berezovska OP, 2006, CELL CYCLE, V5, P1886
[6]   A transgenic mouse model demonstrating the oncogenic role of mutations in the polycomb-group gene EZH2 in lymphomagenesis [J].
Berg, Tobias ;
Thoene, Silvia ;
Yap, Damian ;
Wee, Tracee ;
Schoeler, Nathalie ;
Rosten, Patty ;
Lim, Emilia ;
Bilenky, Misha ;
Mungall, Andrew J. ;
Oellerich, Thomas ;
Lee, Sherry ;
Lai, Courteney K. ;
Umlandt, Patricia ;
Salmi, Anisa ;
Chang, Harry ;
Yue, Lisa ;
Lai, David ;
Cheng, S-W Grace ;
Morin, Ryan D. ;
Hirst, Martin ;
Serve, Hubert ;
Marra, Marco A. ;
Morin, Gregg B. ;
Gascoyne, Randy D. ;
Aparicio, Samuel A. ;
Humphries, R. Keith .
BLOOD, 2014, 123 (25) :3914-3924
[7]   EZH2 is downstream of the pRB-E2F pathway, essential for proliferation and amplified in cancer [J].
Adrian P. Bracken ;
Diego Pasini ;
Maria Capra ;
Elena Prosperini ;
Elena Colli ;
Kristian Helin .
The EMBO Journal, 2003, 22 (20) :5323-5335
[8]  
Butler LM, 2000, CANCER RES, V60, P5165
[9]   Repression of E-cadherin by the polycomb group protein EZH2 in cancer [J].
Cao, Q. ;
Yu, J. ;
Dhanasekaran, S. M. ;
Kim, J. H. ;
Mani, R-S ;
Tomlins, S. A. ;
Mehra, R. ;
Laxman, B. ;
Cao, X. ;
Yu, J. ;
Kleer, C. G. ;
Varambally, S. ;
Chinnaiyan, A. M. .
ONCOGENE, 2008, 27 (58) :7274-7284
[10]   Down-regulation of human DAB2IP gene expression mediated by polycomb Ezh2 complex and histone deacetylase in prostate cancer [J].
Chen, H ;
Tu, SW ;
Hsieh, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (23) :22437-22444