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Utility of VS38c in the diagnostic and prognostic assessment of osteosarcoma and other bone tumours/tumour-like lesions

机译:VS38C在骨骼瘤和其他骨肿瘤/肿瘤样病变的诊断和预后评估中的效用

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VS38c is a monoclonal antibody that recognises a rough endoplasmic reticulum (rER) intracellular antigen termed cytoskeleton-linking membrane protein 63. rER is typically found in viable tumour cells and is abundant in osteosarcoma cells. The aim of this study was to determine the diagnostic and prognostic utility of VS38c in the histological assessment of osteosarcoma and other bone tumours/tumour-like leisons. Immunohistochemical staining with VS38c was carried out on formalin-fixed specimens of osteosarcoma (pre/post-chemotherapy) and a wide range of benign and malignant bone lesions. In addition, VS38c staining of cultures of MG63 and Sa0S2 osteosarcoma cell cultures. (±cisplatin and actinomycin D-treatment) was analysed. VS38c strongly stained tumour cells in all low-grade and high-grade osteosarcomas and in undifferentiated sarcomas and high-grade chondrosarcomas. There was little or no VS38c staining of low-grade chondrosarcomas or chordomas and variable staining of Ewing sarcomas. Osteoblasts in benign bone-forming tumours and mononuclear stromal cells in chondroblastomas, giant cell tumours and non-ossifying fibromas strongly stained for VS38c. VS38c staining was absent in cisplatin and actinomycin D treated Sa0S2 and MG63 cells. In specimens of osteosarcoma post-neoadjuvant therapy, VS38c staining was absent in most morphologically necrotic areas of tumor although some cells with pyknotic nuclei stained for VS38c in these areas. Most tumour cells exhibiting atypical nuclear forms were not stained by VS38c. Our findings show that VS38c is a sensitive but not specific diagnostic marker of osteosarcoma. Staining with VS38c identifies viable osteosarcoma cells, a feature which may be useful in the assessment of percentage tumour necrosis post-neoadjuvant chemotherapy.
机译:VS38C是一种单克隆抗体,其识别粗糙的内质网(RER)细胞内抗原称为胞骨骨架连接膜蛋白63. RER通常在活肿瘤细胞中发现,并且在骨肉瘤细胞中丰富。本研究的目的是确定VS38C在骨肉瘤和其他骨肿瘤/肿瘤的吸血剂的组织学评估中的诊断和预后效用。用VS38C进行免疫组织化学染色对骨肉瘤(预/化疗前/化疗前/后)和广泛的良性和恶性骨病变进行了免疫组织化学染色。此外,MG63和SA0S2骨肉瘤细胞培养物的VS38C染色。 (分析了(±Cisplatin和放线霉素D-处理)。 VS38C在所有低级和高级骨肉瘤和未分化的肉瘤和高档软骨菌瘤中强烈染色的肿瘤细胞。低级软骨肉瘤或eWING肉瘤的可变染色很少或没有VS38C染色。在良性骨形成的肿瘤中的成骨细胞和在软骨细胞瘤中的单核基质细胞,巨细胞瘤和非溶质纤维瘤强烈地染色,对VS38C染色。在顺铂和放线菌素D处理SAO 2和Mg63细胞中不存在VS38C染色。在Neoadjuvant治疗后骨肉瘤的标本中,在肿瘤的大多数形态学上缺乏VS38C染色,尽管在这些区域中具有PS38C的Pyknotic核的一些细胞。表现出非典型核形式的大多数肿瘤细胞未被VS38C染色。我们的研究结果表明,VS38C是骨肉瘤的敏感而非特异性的诊断标志物。用VS38C染色鉴定可行的骨肉瘤细胞,该特征可用于评估肿瘤坏死后新辅助化学疗法的百分比。

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