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手术原位植入可使人类前列腺癌细胞系PC-3在裸鼠体内实现高肺和淋巴结转移表达。

Surgical orthotopic implantation allows high lung and lymph node metastatic expression of human prostate carcinoma cell line PC-3 in nude mice.

作者信息

An Z, Wang X, Geller J, Moossa A R, Hoffman R M

机构信息

AntiCancer Inc., San Diego, California 92111, USA.

出版信息

Prostate. 1998 Feb 15;34(3):169-74. doi: 10.1002/(sici)1097-0045(19980215)34:3<169::aid-pros3>3.0.co;2-d.

Abstract

BACKGROUND

Prostate cancer is the second leading cause of male death in the United States. When diagnosed, nearly half the cases have metastatic lesions. An animal model of human prostate cancer demonstrating spontaneous metastasis from the orthotopic site after tumor implantation should be of great help for us to understand the disease and to formulate treatment strategy. We report here a high metastatic model of human prostate cancer PC-3.

METHODS

We developed microsurgical techniques, termed surgical orthotopic implantation (SOI), to implant histologically intact tumor tissues orthotopically in immunodeficient mice. In this study intact tissue of the human prostate cancer cell line PC-3, harvested from a subcutaneous tumor in a nude mouse, was implanted to the ventral lateral lobes of the prostate gland in a series of nude mice. Mice were sacrificed when found moribund, and autopsy and histology were performed subsequently.

RESULTS

A high frequency of lymph node and lung metastasis was noted upon histological examination. The extensive and widespread lung metastasis following orthotopic implantation of PC-3 is, to the best of our knowledge, the first report in the literature.

CONCLUSIONS

In contrast to orthotopic injection of cell suspensions, no multiple metastatic cell selection was necessary after SOI for significant expression of the metastatic potential of PC-3. We conclude that the stromal tissue architecture maintained in the implanted tumor played a critical role in tumor growth and progression.

摘要

背景

前列腺癌是美国男性死亡的第二大主要原因。在确诊时,近一半的病例已有转移性病变。一种能在肿瘤植入后从原位部位自发转移的人类前列腺癌动物模型,将对我们理解该疾病及制定治疗策略有很大帮助。我们在此报告一种人类前列腺癌PC-3的高转移模型。

方法

我们开发了一种显微外科技术,称为手术原位植入(SOI),将组织学上完整的肿瘤组织原位植入免疫缺陷小鼠体内。在本研究中,从裸鼠皮下肿瘤获取的人类前列腺癌细胞系PC-3的完整组织,被植入一系列裸鼠的前列腺腹外侧叶。当小鼠濒死时将其处死,随后进行尸检和组织学检查。

结果

组织学检查发现淋巴结和肺转移的频率很高。据我们所知,PC-3原位植入后广泛的肺转移是文献中的首次报道。

结论

与原位注射细胞悬液不同,SOI后无需进行多次转移细胞选择即可显著表达PC-3的转移潜能。我们得出结论,植入肿瘤中维持的基质组织结构在肿瘤生长和进展中起关键作用。

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