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建立一种评估人前列腺癌细胞诱导的裸鼠骨吸收抑制作用的模型。

Establishment of a model to evaluate inhibition of bone resorption induced by human prostate cancer cells in nude mice.

作者信息

Nemoto R, Kanoh S, Koiso K, Harada M

机构信息

Department of Urology, University of Tsukuba, Japan.

出版信息

J Urol. 1988 Oct;140(4):875-9. doi: 10.1016/s0022-5347(17)41848-9.

Abstract

A model system of human prostate carcinoma in nude mice for searching out a method to protect the bone from cancer cells is described, in which the transplanted human prostate cancer cells were inoculated subcutaneously over the calvaria in nude mice after the periosteum wa disrupted. The tumor induced osteolysis associated with osteoclast proliferation accompanied with reactive new bone formation. This osteolysis was evaluated by measuring the increased area of bone resorption by its reduced opacity to X-ray, and histology. Etidronate disodium, a diphosphonate derivative, at a dose of three mg./kg. and 10 mg./kg. s.c. protected the bone by decreasing the extent of osteolysis as judged by the above criteria. This inhibition was obtained with no apparent effect on the growth of the tumor. These results are discussed in light of recent clinical work, showing that this animal model is a useful tool to test the effect of new drugs against osteolysis of cancer as well as to study the biology of local interaction between bone and cancer cell.

摘要

描述了一种用于寻找保护骨骼免受癌细胞侵害方法的裸鼠人前列腺癌模型系统,其中在破坏骨膜后,将移植的人前列腺癌细胞皮下接种到裸鼠的颅骨上。肿瘤诱导的骨溶解与破骨细胞增殖相关,并伴有反应性新骨形成。通过测量X射线不透光度降低所反映的骨吸收增加面积以及组织学来评估这种骨溶解。二膦酸盐衍生物依替膦酸二钠,以3毫克/千克和10毫克/千克的剂量皮下注射,根据上述标准判断,通过减少骨溶解程度来保护骨骼。这种抑制作用在对肿瘤生长没有明显影响的情况下获得。根据最近的临床工作对这些结果进行了讨论,表明该动物模型是测试新药对癌症骨溶解作用以及研究骨与癌细胞局部相互作用生物学的有用工具。

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