Klein Russell D
Department of Human Nutrition and Cancer Chemoprevention and Support Program, Comprehensive Cancer Center, The Ohio State University, 325 Campbell Hall, Columbus, 43210, USA.
Mutat Res. 2005 Aug 25;576(1-2):111-9. doi: 10.1016/j.mrfmmm.2005.02.012.
The ability to modify the expression of specific genes in the mouse through genetic engineering technologies allows for the generation of previously unavailable models for prostate cancer prevention research. Although animal models have existed for some time for the study of prostate cancer prevention (primarily in the rat), it is uncertain if the mechanisms that drive prostate carcinogenesis in these models are relevant to those in human prostate cancer. Cell culture studies are of limited usefulness because the conditions are inherently artificial. Factors such as relevant physiologic concentrations and metabolism of putative chemoprevention compounds are difficult to model in an in vitro system. These studies also preclude the types of interactions known to occur between multiple cell types in vivo. In addition, all prostate cancer cell lines are already highly progressed and are not representative of the type of cells to which most preventive strategies would be targeted. Due to the advent of genetically engineered mouse (GEM) models, we now have models of prostate cancer that are dependent on molecular mechanisms already implicated in human prostate carcinogenesis. With these models we can perform a variety of experiments that could previously only be done in cell culture or in prostate cancer cell line xenografts. The currently available GEM models of prostate cancer have been extensively reviewed therefore, this review will focus on the types of models available and their usefulness for various types of preclinical studies relevant to prostate cancer prevention.
通过基因工程技术改变小鼠特定基因表达的能力,使得人们能够创建出以往无法获得的前列腺癌预防研究模型。虽然动物模型用于前列腺癌预防研究已有一段时间(主要是在大鼠中),但这些模型中驱动前列腺癌发生的机制是否与人类前列腺癌的机制相关尚不确定。细胞培养研究的作用有限,因为其条件本质上是人为设定的。诸如假定化学预防化合物的相关生理浓度和代谢等因素很难在体外系统中模拟。这些研究也排除了体内多种细胞类型之间已知会发生的相互作用类型。此外,所有前列腺癌细胞系都已经高度进展,并非大多数预防策略所针对的细胞类型的代表。由于基因工程小鼠(GEM)模型的出现,我们现在拥有了依赖于已被证明与人类前列腺癌发生相关的分子机制的前列腺癌模型。利用这些模型,我们可以进行各种以前只能在细胞培养或前列腺癌细胞系异种移植中进行的实验。目前可用的前列腺癌GEM模型已得到广泛综述,因此,本综述将重点关注可用模型的类型及其对与前列腺癌预防相关的各种临床前研究的用途。