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恶性骨肿瘤中nm23蛋白表达的免疫组织化学分析

Immunohistochemical analysis of nm23 protein expression in malignant bone tumors.

作者信息

Oda Y, Walter H, Radig K, Röse I, Neumann W, Roessner A

机构信息

Institute of Pathology, Faculty of Medicine, Ottovon-Guericke University Magdeburg, Germany.

出版信息

J Cancer Res Clin Oncol. 1995;121(11):667-73. doi: 10.1007/BF01218525.

Abstract

Expression levels of nm23 protein in 72 malignant bone tumors comprising 41 osteosarcomas, 22 chondrosarcomas, 6 Ewing's sarcomas, and 2 malignant fibrous histiocytomas were examined immunohistochemically, using anti-nm23 protein polyclonal antibody, and compared with 51 cases of benign bone tumors or tumor-like lesions. Malignant bone tumors showed significantly higher nm23 protein expression than benign bone tumors or tumor-like lesions (P < 0.0001). In chondrosarcoma, nm23 expression increased in high-grade tumors (grade I versus grade II and III: P = 0.0229). In the cases of osteosarcoma, however, grade IV osteosarcomas showed decreased expression of nm23 compared with grade III tumors (P = 0.0122). There was no significant relationship between nm23 expression and histological type. nm23 expression had no correlation with metastatic potential in osteosarcoma, although the therapy was not uniform in our cases. Furthermore, in 6 cases of osteosarcoma and 1 case of Ewing's sarcoma, there was no clear tendency for a decrease of nm23 in the metastatic sites compared with primary sites, as reported in breast cancer. These results showed that, in contrast to reports on breast cancer and experimental models, nm23 protein expression in human bone tumors may be associated with malignant potentiality, except in cases of osteosarcoma.

摘要

使用抗nm23蛋白多克隆抗体,通过免疫组织化学方法检测了72例恶性骨肿瘤中nm23蛋白的表达水平,这些恶性骨肿瘤包括41例骨肉瘤、22例软骨肉瘤、6例尤因肉瘤和2例恶性纤维组织细胞瘤,并与51例良性骨肿瘤或肿瘤样病变进行了比较。恶性骨肿瘤的nm23蛋白表达明显高于良性骨肿瘤或肿瘤样病变(P < 0.0001)。在软骨肉瘤中,nm23表达在高级别肿瘤中增加(I级与II级和III级比较:P = 0.0229)。然而,在骨肉瘤病例中,IV级骨肉瘤与III级肿瘤相比,nm23表达降低(P = 0.0122)。nm23表达与组织学类型之间无显著关系。在骨肉瘤中,nm23表达与转移潜能无关,尽管我们病例中的治疗方法并不统一。此外,在6例骨肉瘤和1例尤因肉瘤中,与乳腺癌报道不同,转移部位的nm23与原发部位相比没有明显降低的趋势。这些结果表明,与乳腺癌报道和实验模型相反,人类骨肿瘤中nm23蛋白表达可能与恶性潜能相关,但骨肉瘤病例除外。

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