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The current state of preclinical prostate cancer animal models.临床前前列腺癌动物模型的现状。
Prostate. 2008 May 1;68(6):629-39. doi: 10.1002/pros.20726.
2
The use of genetically engineered mouse models of prostate cancer for nutrition and cancer chemoprevention research.利用前列腺癌基因工程小鼠模型进行营养与癌症化学预防研究。
Mutat Res. 2005 Aug 25;576(1-2):111-9. doi: 10.1016/j.mrfmmm.2005.02.012.
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Animal models of prostate cancer.前列腺癌动物模型
Methods Mol Med. 2003;81:89-112. doi: 10.1385/1-59259-372-0:89.
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Modeling prostate cancer in mice: limitations and opportunities.在小鼠中模拟前列腺癌:局限性与机遇
J Androl. 2012 Mar-Apr;33(2):133-44. doi: 10.2164/jandrol.111.013987. Epub 2011 Jun 16.
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Preclinical Models of Prostate Cancer: Patient-Derived Xenografts, Organoids, and Other Explant Models.前列腺癌的临床前模型:患者来源的异种移植物、类器官和其他外植体模型。
Cold Spring Harb Perspect Med. 2018 Aug 1;8(8):a030536. doi: 10.1101/cshperspect.a030536.
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Drug discovery in prostate cancer mouse models.前列腺癌小鼠模型中的药物发现
Expert Opin Drug Discov. 2015;10(9):1011-24. doi: 10.1517/17460441.2015.1052790. Epub 2015 Jun 1.
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Generation of a C57BL/6 MYC-Driven Mouse Model and Cell Line of Prostate Cancer.C57BL/6 小鼠 MYC 驱动的前列腺癌模型及细胞系的构建
Prostate. 2016 Sep;76(13):1192-202. doi: 10.1002/pros.23206. Epub 2016 May 26.
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Deciphering cancer complexities in genetically engineered mice.解读基因工程小鼠中的癌症复杂性。
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Clinically Relevant Humanized Mouse Models of Metastatic Prostate Cancer Facilitate Therapeutic Evaluation.临床相关的转移性前列腺癌人源化小鼠模型有助于治疗评估。
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Revisiting HER2 in Prostate Cancer from an Inclusive Perspective: From Biomarkers to Omics.从全面视角重新审视前列腺癌中的HER2:从生物标志物到组学
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Defining the challenges and opportunities for using patient-derived models in prostate cancer research.定义在前列腺癌研究中使用患者来源模型所面临的挑战和机遇。
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Preclinical Imaging of Prostate Cancer.前列腺癌的临床前影像学
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The future of patient-derived xenografts in prostate cancer research.患者来源异种移植在前列腺癌研究中的未来。
Nat Rev Urol. 2023 Jun;20(6):371-384. doi: 10.1038/s41585-022-00706-x. Epub 2023 Jan 17.
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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
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Tomatoes, Lycopene, and Prostate Cancer: What Have We Learned from Experimental Models?番茄、番茄红素与前列腺癌:实验模型给我们带来了哪些启示?
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Development of a novel castration-resistant orthotopic prostate cancer model in New Zealand White rabbit.建立新西兰大白兔新型去势抵抗性前列腺癌模型
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An RNA-Seq-Based Framework for Characterizing Canine Prostate Cancer and Prioritizing Clinically Relevant Biomarker Candidate Genes.基于 RNA-Seq 的犬前列腺癌特征分析及临床相关生物标志物候选基因的优先级排序框架。
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Characterization of a castrate-resistant prostate cancer xenograft derived from a patient of West African ancestry.源自西非裔患者的去势抵抗性前列腺癌异种移植模型的鉴定。
Prostate Cancer Prostatic Dis. 2022 Sep;25(3):513-523. doi: 10.1038/s41391-021-00460-y. Epub 2021 Oct 13.
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Epithelial protein lost in neoplasm (EPLIN) and prostate cancer: lessons learned from the ARCaP model.肿瘤中丢失的上皮蛋白(EPLIN)与前列腺癌:从ARCaP模型中获得的经验教训
Am J Clin Exp Urol. 2021 Aug 25;9(4):264-276. eCollection 2021.

本文引用的文献

1
Prolonged exposure to reduced levels of androgen accelerates prostate cancer progression in Nkx3.1; Pten mutant mice.在Nkx3.1;Pten基因双突变小鼠中,长期暴露于雄激素水平降低的环境会加速前列腺癌的进展。
Cancer Res. 2007 Oct 1;67(19):9089-96. doi: 10.1158/0008-5472.CAN-07-2887.
2
The evolving biology and treatment of prostate cancer.前列腺癌不断发展的生物学特性与治疗方法
J Clin Invest. 2007 Sep;117(9):2351-61. doi: 10.1172/JCI31791.
3
Mouse models of prostate adenocarcinoma with the capacity to monitor spontaneous carcinogenesis by bioluminescence or fluorescence.具有通过生物发光或荧光监测自发癌变能力的前列腺腺癌小鼠模型。
Cancer Res. 2007 Aug 1;67(15):7525-33. doi: 10.1158/0008-5472.CAN-07-0668.
4
Pten inactivation and the emergence of androgen-independent prostate cancer.PTEN失活与雄激素非依赖性前列腺癌的出现。
Cancer Res. 2007 Jul 15;67(14):6535-8. doi: 10.1158/0008-5472.CAN-07-1271.
5
Haploinsufficient prostate tumor suppression by Nkx3.1: a role for chromatin accessibility in dosage-sensitive gene regulation.Nkx3.1对前列腺肿瘤抑制的单倍剂量不足:染色质可及性在剂量敏感基因调控中的作用
J Biol Chem. 2007 Aug 31;282(35):25790-800. doi: 10.1074/jbc.M702438200. Epub 2007 Jun 30.
6
Should the Gleason grading system for prostate cancer be modified to account for high-grade tertiary components? A systematic review and meta-analysis.前列腺癌的Gleason分级系统是否应进行修改以纳入高级别三级成分?一项系统评价和荟萃分析。
Lancet Oncol. 2007 May;8(5):411-9. doi: 10.1016/S1470-2045(07)70136-5.
7
Morphological features of TMPRSS2-ERG gene fusion prostate cancer.TMPRSS2-ERG基因融合前列腺癌的形态学特征。
J Pathol. 2007 May;212(1):91-101. doi: 10.1002/path.2154.
8
Oncomine 3.0: genes, pathways, and networks in a collection of 18,000 cancer gene expression profiles.Oncomine 3.0:18000个癌症基因表达谱集合中的基因、通路和网络
Neoplasia. 2007 Feb;9(2):166-80. doi: 10.1593/neo.07112.
9
Comprehensive assessment of TMPRSS2 and ETS family gene aberrations in clinically localized prostate cancer.临床局限性前列腺癌中TMPRSS2和ETS家族基因畸变的综合评估
Mod Pathol. 2007 May;20(5):538-44. doi: 10.1038/modpathol.3800769. Epub 2007 Mar 2.
10
Expression analysis of imbalanced genes in prostate carcinoma using tissue microarrays.利用组织微阵列分析前列腺癌中失衡基因的表达
Br J Cancer. 2007 Jan 15;96(1):82-8. doi: 10.1038/sj.bjc.6603490. Epub 2006 Dec 5.

临床前前列腺癌动物模型的现状。

The current state of preclinical prostate cancer animal models.

作者信息

Pienta Kenneth J, Abate-Shen Cory, Agus David B, Attar Ricardo M, Chung Leland W K, Greenberg Norman M, Hahn William C, Isaacs John T, Navone Nora M, Peehl Donna M, Simons Jonathon W, Solit David B, Soule Howard R, VanDyke Terry A, Weber Michael J, Wu Lily, Vessella Robert L

机构信息

University of Michigan, Department of Internal Medicine, Ann Arbor, MI, USA.

出版信息

Prostate. 2008 May 1;68(6):629-39. doi: 10.1002/pros.20726.

DOI:10.1002/pros.20726
PMID:18213636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3681409/
Abstract

Prostate cancer continues to be a major cause of morbidity and mortality in men around the world. The field of prostate cancer research continues to be hindered by the lack of relevant preclinical models to study tumorigenesis and to further development of effective prevention and therapeutic strategies. The Prostate Cancer Foundation held a Prostate Cancer Models Working Group (PCMWG) Summit on August 6th and 7th, 2007 to address these issues. The PCMWG reviewed the state of prostate cancer preclinical models and identified the current limitations of cell line, xenograft and genetically engineered mouse models that have hampered the transition of scientific findings from these models to human clinical trials. In addition the PCMWG identified administrative issues that inhibit the exchange of models and impede greater interactions between academic centers and these centers with industry. The PCMWG identified potential solutions for discovery bottlenecks that include: (1) insufficient number of models with insufficient molecular and biologic diversity to reflect human cancer, (2) a lack of understanding of the molecular events that define tumorigenesis, (3) a lack of tools for studying tumor-host interactions, (4) difficulty in accessing model systems across institutions, and (5) addressing why preclinical studies appear not to be predictive of human clinical trials. It should be possible to apply the knowledge gained molecular and epigenetic studies to develop new cell lines and models that mimic progressive and fatal prostate cancer and ultimately improve interventions.

摘要

前列腺癌仍然是全球男性发病和死亡的主要原因。前列腺癌研究领域继续受到缺乏相关临床前模型的阻碍,这些模型用于研究肿瘤发生以及进一步开发有效的预防和治疗策略。前列腺癌基金会于2007年8月6日至7日召开了前列腺癌模型工作组(PCMWG)峰会,以解决这些问题。PCMWG审查了前列腺癌临床前模型的状况,并确定了细胞系、异种移植和基因工程小鼠模型目前存在的局限性,这些局限性阻碍了从这些模型获得的科学发现向人类临床试验的转化。此外,PCMWG还确定了一些行政问题,这些问题抑制了模型的交流,并阻碍了学术中心与这些中心与行业之间的更多互动。PCMWG确定了发现瓶颈的潜在解决方案,包括:(1)模型数量不足,分子和生物学多样性不足以反映人类癌症;(2)对定义肿瘤发生的分子事件缺乏了解;(3)缺乏研究肿瘤与宿主相互作用的工具;(4)跨机构获取模型系统困难;(5)解决为什么临床前研究似乎不能预测人类临床试验的问题。利用分子和表观遗传学研究获得的知识来开发新的细胞系和模型,以模拟进展性和致命性前列腺癌并最终改善干预措施应该是可行的。