Naturally-Occurring Canine Invasive Urothelial Carcinoma: A Model for Emerging Therapies

被引:32
作者
Sommer, Breann C. [1 ]
Dhawan, Deepika [1 ]
Ratliff, Timothy L. [2 ,3 ]
Knapp, Deborah W. [1 ,3 ]
机构
[1] Purdue Univ, Dept Vet Clin Sci, 625 Harrison St, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[3] Purdue Univ, Purdue Univ Ctr Canc Res, W Lafayette, IN 47907 USA
关键词
Urinary bladder cancer; transitional cell carcinoma; urothelial carcinoma; animal models; dog; immunotherapy; targeted therapy; TRANSITIONAL-CELL CARCINOMA; TYROSINE KINASE INHIBITOR; BLADDER-CANCER; URINARY-BLADDER; PHASE-I; SINGLE-ARM; IMMUNOHISTOCHEMICAL EXPRESSION; LISTERIA-MONOCYTOGENES; CHECKPOINT BLOCKADE; MURAMYL TRIPEPTIDE;
D O I
10.3233/BLC-170145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of targeted therapies and the resurgence of immunotherapy offer enormous potential to dramatically improve the outlook for patients with invasive urothelial carcinoma (InvUC). Optimization of these therapies, however, is crucial as only a minority of patients achieve dramatic remission, and toxicities are common. With the complexities of the therapies, and the growing list of possible drug combinations to test, highly relevant animal models are needed to assess and select the most promising approaches to carry forward into human trials. The animal model(s) should possess key features that dictate success or failure of cancer drugs in humans including tumor heterogeneity, genetic-epigenetic crosstalk, immune cell responsiveness, invasive and metastatic behavior, and molecular subtypes (e.g., luminal, basal). While it may not be possible to create these collective features in experimental models, these features are present in naturally-occurring InvUC in pet dogs. Naturally occurring canine InvUC closely mimics muscle-invasive bladder cancer in humans in regards to cellular and molecular features, molecular subtypes, biological behavior (sites and frequency of metastasis), and response to therapy. Clinical treatment trials in pet dogs with InvUC are considered a win-win scenario; the individual dog benefits from effective treatment, the results are expected to help other dogs, and the findings are expected to translate to better treatment outcomes in humans. This review will provide an overview of canine InvUC, the similarities to the human condition, and the potential for dogs with InvUC to serve as a model to predict the outcomes of targeted therapy and immunotherapy in humans.
引用
收藏
页码:149 / 159
页数:11
相关论文
共 111 条
[1]   Integrative epigenomic analysis of differential DNA methylation in urothelial carcinoma [J].
Aine, Mattias ;
Sjodahl, Gottfrid ;
Eriksson, Pontus ;
Veerla, Srinivas ;
Lindgren, David ;
Ringner, Markus ;
Hoglund, Mattias .
GENOME MEDICINE, 2015, 7
[2]  
[Anonymous], 2010, JAVMA-J AM VET MED A, V236, P495, DOI 10.2460/javma.236.5.488
[3]  
[Anonymous], RFACA17001 US DEP HH
[4]   Atezolizumab as first-line treatment in cisplatin-ineligible patients with locally advanced and metastatic urothelial carcinoma: a single-arm, multicentre, phase 2 trial [J].
Balar, Arjun V. ;
Galsky, Matthew D. ;
Rosenberg, Jonathan E. ;
Powles, Thomas ;
Petrylak, Daniel P. ;
Bellmunt, Joaquim ;
Loriot, Yohann ;
Necchi, Andrea ;
Hoffman-Censits, Jean ;
Perez-Gracia, Jose Luis ;
Dawson, Nancy A. ;
van der Heijden, Michiel S. ;
Dreicer, Robert ;
Srinivas, Sandy ;
Retz, Margitta M. ;
Joseph, Richard W. ;
Drakaki, Alexandra ;
Vaishampayan, Ulka N. ;
Sridhar, Srikala S. ;
Quinn, David I. ;
Duran, Ignacio ;
Shaffer, David R. ;
Eigl, Bernhard J. ;
Grivas, Petros D. ;
Yu, Evan Y. ;
Li, Shi ;
Kadel, Edward E., III ;
Boyd, Zachary ;
Bourgon, Richard ;
Hegde, Priti S. ;
Mariathasan, Sanjeev ;
Thastrom, AnnChristine ;
Abidoye, Oyewale O. ;
Fine, Gregg D. ;
Bajorin, Dean F. .
LANCET, 2017, 389 (10064) :67-76
[5]   Identification and prognostic significance of an epithelial-mesenchymal transition expression profile in human bladder tumors [J].
Baumgart, Egbert ;
Cohen, Michael S. ;
Neto, Brasil Silva ;
Jacobs, Micah A. ;
Wotkowicz, Chad ;
Rieger-Christ, Kimberly M. ;
Biolo, Andreia ;
Zeheb, Ron ;
Loda, Massimo ;
Libertino, John A. ;
Summerhayes, Ian C. .
CLINICAL CANCER RESEARCH, 2007, 13 (06) :1685-1694
[6]   Pembrolizumab as Second-Line Therapy for Advanced Urothelial Carcinoma [J].
Bellmunt, J. ;
de Wit, R. ;
Vaughn, D. J. ;
Fradet, Y. ;
Lee, J. -L. ;
Fong, L. ;
Vogelzang, N. J. ;
Climent, M. A. ;
Petrylak, D. P. ;
Choueiri, T. K. ;
Necchi, A. ;
Gerritsen, W. ;
Gurney, H. ;
Quinn, D. I. ;
Culine, S. ;
Sternberg, C. N. ;
Mai, Y. ;
Poehlein, C. H. ;
Perini, R. F. ;
Bajorin, D. F. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (11) :1015-1026
[7]   A review on the evolution of PD-1/PD-L1 immunotherapy for bladder cancer: The future is now [J].
Bellmunt, Joaquin ;
Powles, Thomas ;
Vogelzang, Nicholas J. .
CANCER TREATMENT REVIEWS, 2017, 54 :58-67
[8]   Inhibiting Immune Checkpoints for the Treatment of Bladder Cancer [J].
Bidnur, S. ;
Savdie, R. ;
Black, P. C. .
BLADDER CANCER, 2016, 2 (01) :15-25
[9]   Promoter hypermethylation of tumor suppressor genes correlates with tumor grade and invasiveness in patients with urothelial bladder cancer [J].
Bilgrami, Shumaila M. ;
Qureshi, Sohail A. ;
Pervez, Shahid ;
Abbas, Farhat .
SPRINGERPLUS, 2014, 3 :1-9
[10]   Immune-based mechanisms of cytotoxic chemotherapy: implications for the design of novel and rationale-based combined treatments against cancer [J].
Bracci, L. ;
Schiavoni, G. ;
Sistigu, A. ;
Belardelli, F. .
CELL DEATH AND DIFFERENTIATION, 2014, 21 (01) :15-25