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实验性鼠类原发性高级未分化多形性肉瘤模型,未另作具体说明。

Experimental murine model of primary high grade undifferentiated pleomorphic sarcoma not otherwise specified.

机构信息

Reference Centre for Soft Tissue Sarcoma, Department of Plastic Surgery, BG University Hospital Bergmannsheil, Ruhr University Bochum, Bürkle-de-la-Camp-Platz 1, 44789 Bochum, North Rhine-Westphalia, Germany.

出版信息

In Vivo. 2012 Jul-Aug;26(4):559-63.

Abstract

BACKGROUND

Undifferentiated pleomorphic sarcoma not otherwise specified (NOS) is a malignant neoplasm of uncertain origin arising both in the soft tissue and the bone. The WHO classified this tumour in 2002 but controversy has plagued this entity due to limited availability of tissue for study. The aim of this study was to establish a reproducible xenograft model of primary human undifferentiated pleomorphic sarcoma NOS.

MATERIALS AND METHODS

Primary human sarcoma samples were divided into tumour fragments and transplanted subcutaneously in mice. Sarcoma xenografts were analysed histolomorphologically (light/electron-microscopy; immunohistochemistry).

RESULTS

All tumours resulted in viable sarcoma NOS xenografts demonstrating similar histological patterns. In both the original tumours and the xenografts, tumour necrosis was found ranging from 15% to 25%. The background stroma of the xenografts was hyalinised like the primary sarcoma. Electron microscopical analyses showed good maintenance of ultrastructure.

CONCLUSION

Implantation of intact tumor fragments yielded in a complete tumor take rate. The development of new cancer therapeutics requires animal models that closely resemble the human patient. This study provides ideal animal models for the research of pathogenesis and pathobiology of primary human undifferentiated pleomorphic sarcoma NOS.

摘要

背景

未分化多形性肉瘤(NOS)是一种起源不明的恶性肿瘤,可发生于软组织和骨骼。2002 年,世界卫生组织(WHO)对该肿瘤进行了分类,但由于可供研究的组织有限,该实体存在争议。本研究旨在建立一种可重现的原发性人类未分化多形性肉瘤 NOS 的异种移植模型。

材料和方法

将原发性人类肉瘤样本分为肿瘤碎片,并皮下移植到小鼠中。对肉瘤异种移植物进行组织形态学分析(光镜/电镜;免疫组织化学)。

结果

所有肿瘤均产生了有活力的未分化多形性肉瘤 NOS 异种移植物,表现出相似的组织学模式。在原发肿瘤和异种移植物中,均发现了 15%至 25%的肿瘤坏死。异种移植物的背景基质呈玻璃样变性,类似于原发性肉瘤。电镜分析显示超微结构得到了很好的维持。

结论

完整肿瘤碎片的植入可获得完全的肿瘤接种率。新癌症治疗方法的开发需要与人类患者非常相似的动物模型。本研究为原发性人类未分化多形性肉瘤 NOS 的发病机制和病理生物学研究提供了理想的动物模型。

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