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A TRAMP‐derived orthotopic prostate syngeneic (TOPS) cancer model for investigating anti‐tumor treatments
Author(s) -
Lardizabal Justin,
Ding Jun,
Delwar Zahid,
Rennie Paul S.,
Jia William
Publication year - 2018
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23490
Subject(s) - tramp , oncolytic virus , prostate cancer , medicine , bioluminescence imaging , prostate , cancer research , cancer , tumor progression , animal model , oncology , pathology , luciferase , biology , cell culture , transfection , genetics
Background Patients with advanced prostate cancer have limited curative options, therefore new treatments are needed. Mouse models play a pivotal role in the discovery and development of new treatments. In the present study, a TRAMP‐derived Orthotopic Prostate Syngeneic (TOPS) mouse model was developed and found to provide a consistent means of monitoring tumor and metastatic responses to novel treatments. Methods The mouse TOPS model was generated using luciferase transduced TRAMP‐C2 prostate cancer cells that were orthotopically injected into Bl6 mice by ultrasound guidance. Tumor growth and development was monitored using ultrasound and bioluminescence imaging. Results Tumors and metastases were consistently established and increases in tumor size correlated with increases in bioluminescence. In addition, when mice with an established tumor were castrated, tumor progression mirrored clinical progression. We further treated the TOPS model with an oncolytic Herpes Simplex virus and showed that we were able to monitor the therapeutic effect of the orthotopic tumor after virus treatment through IVIS imaging system. Conclusion We have developed a powerful animal model to advance the current selection of effective treatments for patients with advanced prostate cancer.