VS38c在骨肉瘤和其他骨肿瘤/肿瘤样病变诊断和预后评估中的应用

Clinical Sarcoma Research Pub Date : 2017-09-18 eCollection Date: 2017-01-01 DOI:10.1186/s13569-017-0083-5
E S Hookway, Z Orosz, Y Uchihara, A Grigoriadis, A B Hassan, U Oppermann, N A Athanasou
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引用次数: 2

摘要

背景:VS38c是一种单克隆抗体,可识别称为细胞骨架连接膜蛋白63的粗糙内质网(rER)细胞内抗原。内质rER通常存在于活的肿瘤细胞中,在骨肉瘤细胞中含量丰富。本研究的目的是确定VS38c在骨肉瘤和其他骨肿瘤/肿瘤样病变的组织学评估中的诊断和预后效用。方法:对化疗前/化疗后的骨肉瘤和各种良恶性骨病变进行福尔马林固定标本的免疫组化VS38c染色。此外,MG63和Sa0S2骨肉瘤细胞培养物的VS38c染色。(±顺铂和放线菌素d治疗)分析。结果:在所有低级别和高级别骨肉瘤以及未分化肉瘤和高级别软骨肉瘤中,VS38c强烈染色肿瘤细胞。低级别软骨肉瘤或脊索瘤的VS38c染色很少或没有,Ewing肉瘤的v38c染色变化。良性成骨肿瘤中的成骨细胞和成软骨细胞瘤、巨细胞瘤和非骨化纤维瘤中的单核间质细胞强烈表达VS38c。顺铂和放线菌素D处理的Sa0S2和MG63细胞未见VS38c染色。在新辅助治疗后的骨肉瘤标本中,大多数肿瘤形态学坏死区域未见VS38c染色,尽管在这些区域有一些核固缩细胞染色。大多数具有非典型核形态的肿瘤细胞未被VS38c染色。结论:我们的研究结果表明VS38c是骨肉瘤的一个敏感但非特异性的诊断标志物。VS38c染色可识别活骨肉瘤细胞,这一特征可用于评估新辅助化疗后肿瘤坏死百分比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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