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MNU加睾酮诱发前列腺癌的大鼠模型

The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis.

作者信息

Bosland Maarten C, Schlicht Michael J, Horton Lori, McCormick David L

机构信息

University of Illinois at Chicago, Chicago, Illinois, USA.

New York University School of Medicine, New York City, New York, USA.

出版信息

Toxicol Pathol. 2022 Jun;50(4):478-496. doi: 10.1177/01926233221096345. Epub 2022 May 19.

DOI:10.1177/01926233221096345
PMID:35588266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9347216/
Abstract

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.

摘要

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。

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The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis.MNU加睾酮诱发前列腺癌的大鼠模型
Toxicol Pathol. 2022 Jun;50(4):478-496. doi: 10.1177/01926233221096345. Epub 2022 May 19.
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Influence of N-methyl-N-nitrosourea, testosterone, and N-(4-hydroxyphenyl)-all-trans-retinamide on prostate cancer induction in Wistar-Unilever rats.N-甲基-N-亚硝基脲、睾酮和N-(4-羟基苯基)-全反式维甲酸对Wistar-联合利华大鼠前列腺癌诱导的影响。
Cancer Res. 1998 Aug 1;58(15):3282-8.
5
Animal models for the study of prostate carcinogenesis.用于前列腺癌发生研究的动物模型。
J Cell Biochem Suppl. 1992;16H:89-98. doi: 10.1002/jcb.240501221.
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Prostate carcinogenesis induced by N-methyl-N-nitrosourea (mnu) in gerbils: histopathological diagnosis and potential invasiveness mediated by extracellular matrix components.N-甲基-N-亚硝脲(mnu)诱导沙鼠前列腺癌发生:细胞外基质成分介导的组织病理学诊断和潜在侵袭性。
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Intravenous vs. intraprostatic administration of N-methyl-N-nitrosourea to induce prostate cancer in rats.静脉注射与前列腺内注射N-甲基-N-亚硝基脲诱导大鼠前列腺癌
Prostate. 1996 Jan;28(1):32-43. doi: 10.1002/(SICI)1097-0045(199601)28:1<32::AID-PROS5>3.0.CO;2-Q.
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Chemoprevention of rat prostate carcinogenesis by early and delayed administration of dehydroepiandrosterone.早期和延迟给予脱氢表雄酮对大鼠前列腺癌发生的化学预防作用。
Cancer Res. 1999 Jul 1;59(13):3084-9.
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Chemopreventive effects of zinc on prostate carcinogenesis induced by N-methyl-N-nitrosourea and testosterone in adult male Sprague-Dawley rats.锌对 N-甲基-N-亚硝脲和睾酮诱导的成年雄性 Sprague-Dawley 大鼠前列腺癌发生的化学预防作用。
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Successful hormonal and chemical induction of prostate cancer in a rat model: practical guidelines.大鼠模型中前列腺癌的成功激素和化学诱导:实用指南。
Vet Res Forum. 2024;15(9):445-453. doi: 10.30466/vrf.2023.1999343.3838. Epub 2024 Sep 15.
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Testosterone Nanoemulsion Prevents Prostate Cancer: PC-3 and LNCaP Cell Viability In Vitro.睾酮纳米乳剂可预防前列腺癌:体外 PC-3 和 LNCaP 细胞活力。
Int J Mol Sci. 2024 Jul 15;25(14):7729. doi: 10.3390/ijms25147729.
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OBSERVE: guidelines for the refinement of rodent cancer models.注意:啮齿类动物癌症模型改良指南。

本文引用的文献

1
Development of the human prostate.人类前列腺的发育
Differentiation. 2018 Sep-Oct;103:24-45. doi: 10.1016/j.diff.2018.08.005. Epub 2018 Sep 4.
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Genetically Engineered Mouse Models of Prostate Cancer in the Postgenomic Era.在后基因组时代的前列腺癌基因工程小鼠模型。
Cold Spring Harb Perspect Med. 2019 Feb 1;9(2):a030528. doi: 10.1101/cshperspect.a030528.
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Induction of a heparin-stimulated serine proteinase in sex accessory gland tumors of the Lobund-Wistar rat.在Lobund-Wistar大鼠的性附属腺肿瘤中诱导产生一种肝素刺激的丝氨酸蛋白酶。
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Arsenic-induced prostate cancer: an enigma.砷诱导的前列腺癌:一个谜。
Med Oncol. 2024 Jan 6;41(2):50. doi: 10.1007/s12032-023-02266-5.
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Lifelong exercise training promotes the remodelling of the immune system and prostate signalome in a rat model of prostate carcinogenesis.终身运动训练可促进前列腺癌发生大鼠模型中免疫系统和前列腺信号组的重塑。
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Effects of perinatal exposure to bisphenol A on induction of prostate cancer in Sprague Dawley rats by MNU and testosterone.围生期双酚 A 暴露对 MNU 和睾酮诱导 Sprague Dawley 大鼠前列腺癌的影响。
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Validation of the Rat Model of Prostate Cancer: Correlating Seminal Vesicle Lesions With Dorsolateral Prostate Lesions.前列腺癌大鼠模型的验证:与背外侧前列腺病变相关的精囊病变。
In Vivo. 2022 Nov-Dec;36(6):2662-2668. doi: 10.21873/invivo.13001.
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Effect of Dietary Methylseleninic Acid and Se-Methylselenocysteine on Carcinogen-Induced, Androgen-Promoted Prostate Carcinogenesis in Rats.膳食甲基硒酸和硒代蛋氨酸对致癌物诱导的雄激素促进的大鼠前列腺癌发生的影响。
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Exp Mol Pathol. 2015 Aug;99(1):39-43. doi: 10.1016/j.yexmp.2015.04.008. Epub 2015 Apr 22.
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Testosterone treatment is a potent tumor promoter for the rat prostate.睾酮治疗是大鼠前列腺的一种强效肿瘤促进剂。
Endocrinology. 2014 Dec;155(12):4629-33. doi: 10.1210/en.2014-1688. Epub 2014 Sep 23.
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Mouse models of prostate cancer: picking the best model for the question.前列腺癌小鼠模型:为问题选择最佳模型。
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Animal models of human prostate cancer: the consensus report of the New York meeting of the Mouse Models of Human Cancers Consortium Prostate Pathology Committee.人类前列腺癌动物模型:人类癌症小鼠模型联盟前列腺病理学委员会纽约会议共识报告。
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Vitamin E and the risk of prostate cancer: the Selenium and Vitamin E Cancer Prevention Trial (SELECT).维生素 E 与前列腺癌风险:硒和维生素 E 癌症预防试验(SELECT)。
JAMA. 2011 Oct 12;306(14):1549-56. doi: 10.1001/jama.2011.1437.
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Null activity of selenium and vitamin e as cancer chemopreventive agents in the rat prostate.硒和维生素 E 作为癌症化学预防剂在大鼠前列腺中无活性。
Cancer Prev Res (Phila). 2010 Mar;3(3):381-92. doi: 10.1158/1940-6207.CAPR-09-0176. Epub 2010 Feb 9.