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连续异体移植的人前列腺肿瘤作为实验模型。

Serially heterotransplanted human prostate tumours as an experimental model.

机构信息

Stanley S. Scott Cancer Center, Louisiana State University, Health Sciences Center, New Orleans, LA 70112, USA.

出版信息

J Cell Mol Med. 2010 Jun;14(6B):1385-95. doi: 10.1111/j.1582-4934.2009.00957.x. Epub 2009 Oct 29.

Abstract
  • Introduction * Serially heterotransplanted human tumours in immunosuppressed mice: similarity to the tumour of origin - Cytological and histological analysis - Karyotype - Marker expression - Other PC markers - Tumour cell proliferation and frequency of mitosis - Vasculature - Stromal compartment - Heterotransplant hormone dependency - Androgen dependent - Partially androgen dependent - Androgen independent - Metastases * Conclusions Preclinical research on prostate cancer (PC) therapies uses several models to represent the human disease accurately. A common model uses patient prostate tumour biopsies to develop a cell line by serially passaging and subsequent implantation, in immunodeficient mice. An alternative model is direct implantation of patient prostate tumour biopsies into immunodeficient mice, followed by serial passage in vivo. The purpose of this review is to compile data from the more than 30 years of human PC serial heterotransplantation research. Serially heterotransplanted tumours are characterized by evaluating the histopathology of the resulting heterotransplants, including cellular differentiation, karyotype, marker expression, hormone sensitivity, cellular proliferation, metastatic potential and stromal and vascular components. These data are compared with the initial patient tumour specimen and, depending on available information, the patient's clinical outcome was compared with the heterotransplanted tumour. The heterotansplant model is a more accurate preclinical model than older generation serially passaged or genetic models to investigate current and newly developed androgen-deprivation agents, antitumour compounds, anti-angiogenic drugs and positron emission tomography radiotracers, as well as new therapeutic regimens for the treatment of PC.
摘要
  • 介绍 * 在免疫抑制小鼠中连续异种移植的人肿瘤:与起源肿瘤的相似性 - 细胞学和组织学分析 - 核型 - 标志物表达 - 其他 PC 标志物 - 肿瘤细胞增殖和有丝分裂频率 - 脉管系统 - 基质区室 - 异种移植激素依赖性 - 雄激素依赖性 - 部分雄激素依赖性 - 雄激素非依赖性 - 转移 * 结论 前列腺癌 (PC) 治疗的临床前研究使用几种模型来准确代表人类疾病。一种常见的模型使用患者前列腺肿瘤活检通过连续传代和随后的植入,在免疫缺陷小鼠中开发细胞系。另一种替代模型是直接将患者的前列腺肿瘤活检植入免疫缺陷小鼠中,然后在体内进行连续传代。本综述的目的是编译超过 30 年的人 PC 连续异种移植研究数据。连续异种移植肿瘤的特征是通过评估异种移植的组织病理学来评价,包括细胞分化、核型、标志物表达、激素敏感性、细胞增殖、转移潜能以及基质和血管成分。这些数据与初始患者肿瘤标本进行比较,并且根据可用信息,将患者的临床结果与异种移植肿瘤进行比较。与较旧的连续传代或遗传模型相比,异种移植模型是一种更准确的临床前模型,可用于研究当前和新开发的雄激素剥夺剂、抗肿瘤化合物、抗血管生成药物和正电子发射断层扫描放射性示踪剂,以及用于治疗 PC 的新治疗方案。

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