Genetically defined mouse models that mimic natural aspects of human prostate cancer development.

2004 ◽  
Vol 11 (2) ◽  
pp. 225-254 ◽  
Author(s):  
P Roy-Burman ◽  
H Wu ◽  
W C Powell ◽  
J Hagenkord ◽  
M B Cohen

This review is focused on mouse models for prostate cancer that have been designed on the basis of genetic alterations that are frequently found in human prostate cancer. It begins with an analysis of the similarities and differences in the gross and microscopic anatomy of the mouse and human prostate glands, and extends to the pathologies induced in the genetically manipulated mouse prostate in comparison with the sporadic development of the disease in humans. Major achievements have been made in modeling human prostate cancer in mice in recent years. There are models which display slow, temporal development of increasingly severe preneoplastic lesions, which are remarkably restricted to the prostate gland, a property similar to the aging-related progression of these lesions in humans. Other models rapidly progress to local invasive adenocarcinoma, and, in some of them metastasis is manifested subsequently with defined kinetics. Global assessment of molecular changes in the prostate of the genetically manipulated mice is increasingly underscoring the validity of the models through identification of 'signature' genes which are associated with the organ-confined primary or distant metastases of human prostate cancer. Taken together, various 'natural' models depicting stages of the disease, ranging from the early preneoplastic lesions to metastatic prostate cancer, now provide new tools both for exploring the molecular mechanism underlying prostate cancer and for development or testing of new targeted therapies.

2006 ◽  
Vol 237 (2) ◽  
pp. 298-304 ◽  
Author(s):  
Jas Singh ◽  
Pachiappan Manickam ◽  
Michael Shmoish ◽  
Sara Natik ◽  
Gareth Denyer ◽  
...  

Author(s):  
Imran Ahmad ◽  
Owen J. Sansom ◽  
Hing Y. Leung

Advances in science and technology have allowed us to manipulate the mouse genome and analyse the effect of specific genetic alterations on the development of prostate cancer in vivo. We can now analyse the molecular basis of initiation, invasion and progression to metastatic disease. The current mouse models utilise knockout, knock-in or conditional regulation of expression using Cre–loxP technology. Genes that have been targeted include homeobox genes, tumour suppressors and oncogenes, growth factors (and their receptors), steroid hormones and cell-cycle regulators, as well as pro- and anti-apoptotic proteins. Bigenic models indicate that that two ‘hits’ are required for progression from intra-epithelial neoplasia (PIN) to invasion carcinoma, and two to five hits are needed for metastasis. Here, we discuss the numerous models that mimic various aspects of the disease process, such as PIN, locally invasive adenocarcinoma and metastatic disease. Currently the PB-Cre4 × PTENloxP/loxP mouse is the only model that spans the entire continuum from initiation to local invasion and metastasis. Such mouse models increase our understanding of the disease process and provide targets for novel therapeutic approaches. Hopefully, the transgenic models will become inducible and ultimately allow both temporal and spatial gene inactivation. Compound mutational models will also develop further, with double and triple knock-in or knockout systems adding to our knowledge of the interaction between different signalling cascades.


2019 ◽  
Vol 21 (6) ◽  
pp. 1054-1063 ◽  
Author(s):  
Ben T. Copeland ◽  
Hassan Shallal ◽  
Chentian Shen ◽  
Kenneth J. Pienta ◽  
Catherine A. Foss ◽  
...  

Cell Reports ◽  
2015 ◽  
Vol 12 (12) ◽  
pp. 2060-2071 ◽  
Author(s):  
Antonina Mitrofanova ◽  
Alvaro Aytes ◽  
Min Zou ◽  
Michael M. Shen ◽  
Cory Abate-Shen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document