Models of metastatic prostate cancer: a transgenic perspective
- PMID: 12970722
- DOI: 10.1038/sj.pcan.4500655
Models of metastatic prostate cancer: a transgenic perspective
Abstract
Purpose: Transgenic mouse models are proving to be invaluable in our effort to understand the molecular basis of metastatic prostate cancer (CaP). We review and discuss how current animal models have contributed to our understanding of the metastatic cascade and how transgenic technology is being used to develop the next generation of mouse models. Our goal is to provide a review of the recent advances and provide a framework for further studies.
Materials and methods: We performed a MEDLINE search of the literature on CaP metastasis transgenic and animal models.
Results: We present a summary of the characteristics of nine different animal models of CaP. Each model is unique and provides valuable insight into the molecular mechanisms governing the progression of CaP. Our experience with transgenic models and all the new data from the literature predicts that we will be able to develop genetically engineered mice that accurately mimic the heterogeneity, androgen-independent growth, and metastatic spread seen in clinical disease.
Conclusion: In order to elucidate the molecular mechanisms of CaP metastasis, it will be necessary to compare gene and protein expression patterns and biochemical analyses of clinical metastatic disease with data obtained from current models. We will also need to refine our ability to engineer and characterize genetic perturbation models. This type of integrative and iterative approach should facilitate better understanding of the molecular biology of CaP metastases.
Similar articles
-
Survey of genetically engineered mouse models for prostate cancer: analyzing the molecular basis of prostate cancer development, progression, and metastasis.J Cell Biochem. 2005 Feb 1;94(2):279-97. doi: 10.1002/jcb.20339. J Cell Biochem. 2005. PMID: 15565647 Review.
-
Autochthonous mouse models for prostate cancer: past, present and future.Semin Cancer Biol. 2001 Jun;11(3):245-60. doi: 10.1006/scbi.2001.0373. Semin Cancer Biol. 2001. PMID: 11407949 Review.
-
Genetically modified mice and their use in developing therapeutic strategies for prostate cancer.J Urol. 2004 Jul;172(1):12-9. doi: 10.1097/01.ju.0000132122.93436.aa. J Urol. 2004. PMID: 15201729 Review.
-
Knockin of SV40 Tag oncogene in a mouse adenocarcinoma of the prostate model demonstrates advantageous features over the transgenic model.Oncogene. 2005 Feb 24;24(9):1510-24. doi: 10.1038/sj.onc.1208229. Oncogene. 2005. PMID: 15674347
-
A novel knock-in prostate cancer model demonstrates biology similar to that of human prostate cancer and suitable for preclinical studies.Mol Ther. 2005 Mar;11(3):348-62. doi: 10.1016/j.ymthe.2004.12.005. Mol Ther. 2005. PMID: 15727931
Cited by
-
Glipizide suppresses prostate cancer progression in the TRAMP model by inhibiting angiogenesis.Sci Rep. 2016 Jun 13;6:27819. doi: 10.1038/srep27819. Sci Rep. 2016. PMID: 27292155 Free PMC article.
-
Conditional expression of the androgen receptor induces oncogenic transformation of the mouse prostate.J Biol Chem. 2011 Sep 23;286(38):33478-88. doi: 10.1074/jbc.M111.269894. Epub 2011 Jul 27. J Biol Chem. 2011. PMID: 21795710 Free PMC article.
-
In vivo animal models for studying brain metastasis: value and limitations.Clin Exp Metastasis. 2013 Jun;30(5):695-710. doi: 10.1007/s10585-013-9566-9. Epub 2013 Jan 16. Clin Exp Metastasis. 2013. PMID: 23322381 Review.
-
HTLV-1 Tax transgenic mice develop spontaneous osteolytic bone metastases prevented by osteoclast inhibition.Blood. 2005 Dec 15;106(13):4294-302. doi: 10.1182/blood-2005-04-1730. Epub 2005 Aug 23. Blood. 2005. PMID: 16118323 Free PMC article.
-
Tumor cell transendothelial passage in the absorbing lymphatic vessel of transgenic adenocarcinoma mouse prostate.Am J Pathol. 2007 Jan;170(1):334-46. doi: 10.2353/ajpath.2007.060447. Am J Pathol. 2007. PMID: 17200205 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous