犬局限性前列腺癌模型的病理学研究。

IF 2.5 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Prostate Pub Date : 2025-09-22 DOI:10.1002/pros.70054
Nathan K Hoggard, Felipe M Berg, Marlon R Szczepaniak, Xinning Wang, Noriko Kantake, Gopalakrishnan Ramamurthy, Li Gong, Eric T Hostnik, Krishan Kumar, Arijit Ghosh, Dong Luo, Michael V Knopp, Jill M Keller, Evan T Keller, Agata A Exner, James P Basilion, Michael F Tweedle, Thomas J Rosol
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引用次数: 0

摘要

背景:狗会自发患上前列腺癌(PC),其前列腺解剖、生理和大小与人类相同。在过去的15年中,我们已经开发并完善了犬局灶性PC模型,以评估治疗诊断(治疗)干预措施。尚未对病理和各种研究的综合进行全面的描述。该手稿的目的是描述其方法学发展框架内的犬模型肿瘤病理,以帮助指导未来的翻译PC研究。方法:在已发表和未发表的研究中,我们先前用转染人类或犬基因的犬PC细胞系(Ace-1)接种免疫抑制的完整比格犬(n = 56)的前列腺,用于靶向治疗。所有病例均行大体肿瘤评估和组织学检查。采用数字图像分析、免疫组织化学、激光显微解剖和实时荧光定量PCR对分子肿瘤和微环境病理进行了研究。结果:该模型可靠地(85.7%的植入率)形成了类似中、高度局限性PC的前列腺肿瘤,形态分化差,间质浸润,外周生长。48只狗中有13只(27.1%)发生软组织转移。大多数狗形成多灶性前列腺肿瘤,偶有前列腺外肿瘤。肿瘤位置影响生长行为和微环境。同种异体移植物在组织学上分为腺体内前列腺内、浸润性前列腺内、囊状或前列腺外。与前列腺内肿瘤相比,包膜/前列腺外肿瘤的增殖(Ki-67指数)、上皮向间质转化以及微环境改变(包括胶原间质增加、纤维增生和免疫细胞浸润减少)增加。结论:犬PC模型捕获了接受治疗意图治疗的男性的重要病理特征,以及研究人员感兴趣的模型和物种特异性特征。除了定义病理学外,研究结果还强调了犬模型在研究肿瘤微环境和推进大型动物临床前抗癌策略方面的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathology of a Canine Model of Localized Prostate Carcinoma.

Background: Dogs spontaneously develop prostate carcinoma (PC) and share prostate gland anatomy, physiology, and size to men. Over the last 15 years, we have developed and refined a canine model of focal PC to evaluate therapeutic-diagnostic (theranostic) interventions. A comprehensive description of the pathology and synthesis of the various studies has not been performed. The goal of this manuscript was to describe the canine model tumor pathology within the framework of its methodological development to help guide future translational PC research.

Methods: In published and unpublished studies, we previously inoculated prostate glands of immunosuppressed, intact beagle dogs (n = 56) with a canine PC cell line (Ace-1) transduced with human or canine genes for targeted theranostics. Gross tumor assessment and histology were performed in all cases. Molecular tumor and microenvironmental pathology was investigated using digital image analysis, immunohistochemistry, laser-capture microdissection, and quantitative real-time PCR.

Results: The model reliably (85.7% engraftment rate) formed prostatic tumors resembling intermediate and high-grade localized PC, with poorly differentiated morphology, stromal invasion, and peripheral growth. Soft tissue metastasis occurred in 13/48 (27.1%) dogs. Most dogs formed multifocal prostatic tumors with occasional tumors outside the prostate gland. Tumor location influenced growth behavior and the microenvironment. Allografts were histologically classified as intraglandular intraprostatic, invasive intraprostatic, capsular, or extraprostatic. Compared to intraprostatic tumors, capsular/extraprostatic tumors had increased proliferation (Ki-67 index), epithelial-to-mesenchymal transition, and microenvironmental alterations that included increased collagenous stroma, fibroplasia, and reduced immune cell infiltration.

Conclusions: The canine model of PC captured important pathologic features of men undergoing curative-intent therapy alongside model- and species-specific characteristics of interest to researchers. Beyond defining pathology, the results highlighted applications of the canine model in studying the tumor microenvironment and advancing preclinical, anti-cancer strategies in a large animal species.

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来源期刊
Prostate
Prostate 医学-泌尿学与肾脏学
CiteScore
5.10
自引率
3.60%
发文量
180
审稿时长
1.5 months
期刊介绍: The Prostate is a peer-reviewed journal dedicated to original studies of this organ and the male accessory glands. It serves as an international medium for these studies, presenting comprehensive coverage of clinical, anatomic, embryologic, physiologic, endocrinologic, and biochemical studies.
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