Genetically engineered murine models - Contribution to our understanding of the genetics, molecular pathology and therapeutic targeting of neuroblastoma

被引:46
作者
Chesler, Louis [1 ,2 ]
Weiss, William A. [3 ,4 ,5 ,6 ]
机构
[1] Inst Canc Res, Div Clin Studies & Canc Therapeut, Sutton SM2 5NG, Surrey, England
[2] Royal Marsden NHS Trust, Sutton SM2 5NG, Surrey, England
[3] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Brain Tumor Res Ctr, Dept Neurol, San Francisco, CA 94158 USA
[5] Univ Calif San Francisco, Brain Tumor Res Ctr, Dept Pediat, San Francisco, CA 94158 USA
[6] Univ Calif San Francisco, Brain Tumor Res Ctr, Dept Neurol Surg, San Francisco, CA 94158 USA
关键词
MYCN; Neuroblastoma; Mouse models; TUMOR-SUPPRESSOR GENE; MINIMAL RESIDUAL DISEASE; EMBRYONIC STEM-CELLS; N-MYC; INDUCED APOPTOSIS; C-MYC; ACTIVATING MUTATIONS; MOUSE MODEL; MALIGNANT PROGRESSION; CASPASE-8; EXPRESSION;
D O I
10.1016/j.semcancer.2011.09.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetically engineered mouse models (GEMM) have made major contributions to a molecular understanding of several adult cancers and these results are increasingly being translated into the pre-clinical setting where GEMM will very likely make a major impact on the development of targeted therapeutics in the near future. The relationship of pediatric cancers to altered developmental programs, and their genetic simplicity relative to adult cancers provides unique opportunities for the application of new advances in GEMM technology. In neuroblastoma the well-characterized TH-MYCN GEMM is increasingly used for a variety of molecular-genetic, developmental and pre-clinical therapeutics applications. We discuss: the present and historical application of GEMM to neuroblastoma research, future opportunities, and relevant targets suitable for new GEMM strategies in neuroblastoma. We review the potential of these models to contribute both to an understanding of the developmental nature of neuroblastoma and to improved therapy for this disease. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:245 / 255
页数:11
相关论文
共 163 条
[1]   Pinhole imaging of 131I-metaiodobenzyl-guanidine (131-I-MIBG) in an animal model of neuroblastoma [J].
Accorsi, R ;
Morowitz, MJ ;
Charron, M ;
Maris, JM .
PEDIATRIC RADIOLOGY, 2003, 33 (10) :688-692
[2]  
Agathanggelou A, 2003, CANCER RES, V63, P5344
[3]   CXCR5 may be involved in the attraction of human metastatic neuroblastoma cells to the bone marrow [J].
Airoldi, Irma ;
Cocco, Claudia ;
Morandi, Fabio ;
Prigione, Ignazia ;
Pistoia, Vito .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2008, 57 (04) :541-548
[4]   MYCN Promotes the Expansion of Phox2B-Positive Neuronal Progenitors to Drive Neuroblastoma Development [J].
Alam, Goleeta ;
Cui, Hongjuan ;
Shi, Huilin ;
Yang, Liqun ;
Ding, Jane ;
Mao, Ling ;
Maltese, William A. ;
Ding, Han-Fei .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 175 (02) :856-866
[5]   Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma [J].
Amaravadi, Ravi K. ;
Yu, Duonan ;
Lum, Julian J. ;
Bui, Thi ;
Christophorou, Maria A. ;
Evan, Gerard I. ;
Thomas-Tikhonenko, Andrei ;
Thompson, Craig B. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (02) :326-336
[6]   DRR1 is expressed in the developing nervous system and downregulated during neuroblastoma carcinogenesis [J].
Asano, Yoshizumi ;
Kishida, Satoshi ;
Mu, Ping ;
Sakamoto, Kazuma ;
Murohara, Toyoaki ;
Kadomatsu, Kenji .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 394 (03) :829-835
[7]   PHOX2B-Mediated Regulation of ALK Expression: In Vitro Identification of a Functional Relationship between Two Genes Involved in Neuroblastoma [J].
Bachetti, Tiziana ;
Di Paolo, Daniela ;
Di Lascio, Simona ;
Mirisola, Valentina ;
Brignole, Chiara ;
Bellotti, Marta ;
Caffa, Irene ;
Ferraris, Chiara ;
Fiore, Michele ;
Fornasari, Diego ;
Chiarle, Roberto ;
Borghini, Silvia ;
Pfeffer, Ulrich ;
Ponzoni, Mirco ;
Ceccherini, Isabella ;
Perri, Patrizia .
PLOS ONE, 2010, 5 (10)
[8]   Serial Transcriptome Analysis and Cross-Species Integration Identifies Centromere-Associated Protein E as a Novel Neuroblastoma Target [J].
Balamuth, Naomi J. ;
Wood, Andrew ;
Wang, Qun ;
Jagannathan, Jayanti ;
Mayes, Patrick ;
Zhang, Zhe ;
Chen, Zhongxue ;
Rappaport, Eric ;
Courtright, Joshua ;
Pawel, Bruce ;
Weber, Barbara ;
Wooster, Richard ;
Sekyere, Eric O. ;
Marshall, Glenn M. ;
Maris, John M. .
CANCER RESEARCH, 2010, 70 (07) :2749-2758
[9]   Tet repressor-based system for regulated gene expression in eukaryotic cells: Principles and advances [J].
Baron, U ;
Bujard, H .
APPLICATIONS OF CHIMERIC GENES AND HYBRID PROTEINS PT B: CELL BIOLOGY AND PHYSIOLOGY, 2000, 327 :401-421
[10]   Detecting minimal residual disease in neuroblastoma patients - the present state of the art [J].
Beiske, K ;
Ambros, PF ;
Burchill, SA ;
Cheung, IY ;
Swerts, K .
CANCER LETTERS, 2005, 228 (1-2) :229-240