Valkenburg Kenneth C, Williams Bart O
Van Andel Research Institute, 333 Bostwick Avenue N.E., Grand Rapids, MI 49503, USA.
Prostate Cancer. 2011;2011:895238. doi: 10.1155/2011/895238. Epub 2011 Feb 23.
The development and optimization of high-throughput screening methods has identified a multitude of genetic changes associated with human disease. The use of immunodeficient and genetically engineered mouse models that mimic the human disease has been crucial in validating the importance of these genetic pathways in prostate cancer. These models provide a platform for finding novel therapies to treat human patients afflicted with prostate cancer as well as those who have debilitating bone metastases. In this paper, we focus on the historical development and phenotypic descriptions of mouse models used to study prostate cancer. We also comment on how closely each model recapitulates human prostate cancer.
高通量筛选方法的发展与优化已经识别出众多与人类疾病相关的基因变化。使用免疫缺陷和基因工程小鼠模型来模拟人类疾病,对于验证这些基因通路在前列腺癌中的重要性至关重要。这些模型为寻找新疗法以治疗罹患前列腺癌的人类患者以及患有使人衰弱的骨转移的患者提供了一个平台。在本文中,我们聚焦于用于研究前列腺癌的小鼠模型的历史发展和表型描述。我们还评论了每种模型与人类前列腺癌的相似程度。