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基于胶原蛋白分析的骨肉瘤化疗效果:骨肉瘤分化诱导的提议

Chemotherapeutic effect on osteosarcoma on basis of collagen analysis: a proposal of the induction of osteosarcoma differentiation.

作者信息

Tsuchiya H, Ueda Y, Tomita K, Nakanishi I, Roessner A

机构信息

Department of Orthopaedic Surgery, School of Medicine, Kanazawa University, Ishikawa, Japan.

出版信息

J Cancer Res Clin Oncol. 1993;119(12):702-6. doi: 10.1007/BF01195340.

Abstract

The authors studied effect of chemotherapy on osteosarcoma by collagen analysis. As a result of this case study we propose the induction of osteosarcoma differentiation by chemotherapy. Treatment of a conventional osteosarcoma with two intra-arterial infusions of cisplatin and the T-12 protocol of Rosen resulted in sclerotic changes and good margination accompanied by the disappearance of the soft-tissue component from the X-rays. More than 90% tumour destruction was histologically demonstrated; tumour bone and osteoid increased after the chemotherapy, and the viable area of the tumour resembled an osteoblastoma. Before the chemotherapy, immunolocalization determined collagen types I and V to be diffusely present in the bone and osteoid. After the chemotherapy, the antibody to type I collagen was diffusely present, but the antibody to type V collagen occurred only on the surface of the increased bone and osteoid as in normal bone. When osteosarcoma cells were treated in vitro with methotrexate or cisplatin, collagen production increased significantly. It is thus believed that tumour cells were directly stimulated with these chemotherapeutic agents to produce collagen. The findings suggested that some anticancer agents might not only be cytotoxic to but also differentiate osteosarcoma cells.

摘要

作者通过胶原蛋白分析研究了化疗对骨肉瘤的影响。作为该病例研究的结果,我们提出化疗可诱导骨肉瘤分化。用两次顺铂动脉内输注和罗森的T-12方案治疗传统骨肉瘤,导致硬化改变和良好的边界,同时X线显示软组织成分消失。组织学证明肿瘤破坏超过90%;化疗后肿瘤骨和类骨质增加,肿瘤的存活区域类似成骨细胞瘤。化疗前,免疫定位显示I型和V型胶原蛋白在骨和类骨质中弥漫性存在。化疗后,I型胶原蛋白抗体弥漫性存在,但V型胶原蛋白抗体仅像在正常骨中一样出现在增加的骨和类骨质表面。当骨肉瘤细胞在体外用甲氨蝶呤或顺铂处理时,胶原蛋白产生显著增加。因此认为这些化疗药物直接刺激肿瘤细胞产生胶原蛋白。这些发现表明,一些抗癌药物可能不仅对骨肉瘤细胞具有细胞毒性,还能使其分化。

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本文引用的文献

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Cancer. 1985 Oct 1;56(7):1515-21. doi: 10.1002/1097-0142(19851001)56:7<1515::aid-cncr2820560707>3.0.co;2-6.
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