Bosland Maarten C, Schlicht Michael J, Horton Lori, McCormick David L
University of Illinois at Chicago, Chicago, Illinois, USA.
New York University School of Medicine, New York City, New York, USA.
Toxicol Pathol. 2022 Jun;50(4):478-496. doi: 10.1177/01926233221096345. Epub 2022 May 19.
Animal models of prostate cancer are essential to identify chemopreventive treatments against this major male malignancy. The -methyl--nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and has been used extensively in chemoprevention studies with good predictive value for the results of human clinical trials. The objective of this article is to describe the induction protocol of this model, demonstrate its robustness and reproducibility over time and across rat strains, provide diagnostic criteria for the identification of prostate lesions, and present the current tumor induction protocol so that others can use this model in a reliable manner. The majority of accessory sex gland tumors in this model are adenocarcinomas originating in the anterior and dorsolateral prostate that metastasize to lungs and abdominal structures. The rat strain used is of critical importance, with the commercially available Wistar WU and Fischer F344 strains yielding the highest tumor incidences. Low dose, long-term testosterone treatment is essential for a high tumor incidence, but in advanced stage, large adenocarcinomas do not appear to be androgen dependent. This rat model is a robust and reproducible prostate cancer animal model of human prostate cancer.
前列腺癌动物模型对于确定针对这种主要男性恶性肿瘤的化学预防治疗方法至关重要。甲基亚硝基脲(MNU)加睾酮诱导的大鼠前列腺癌发生模型是一种可靠的动物模型,在许多方面可重现人类前列腺癌,并且已广泛用于化学预防研究,对人类临床试验结果具有良好的预测价值。本文的目的是描述该模型的诱导方案,证明其随时间推移以及在不同大鼠品系中的稳健性和可重复性,提供前列腺病变识别的诊断标准,并介绍当前的肿瘤诱导方案,以便其他人能够可靠地使用该模型。该模型中的大多数附属性腺肿瘤是起源于前列腺前部和背外侧的腺癌,可转移至肺部和腹部结构。所使用的大鼠品系至关重要,市售的Wistar WU和Fischer F344品系产生的肿瘤发生率最高。低剂量、长期的睾酮治疗对于高肿瘤发生率至关重要,但在晚期,大腺癌似乎不依赖雄激素。该大鼠模型是一种用于人类前列腺癌的稳健且可重复的前列腺癌动物模型。