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血管化腹股沟腔室:在裸鼠体内培养原发性人脂肪肉瘤的新模型。

The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice.

作者信息

Tilkorn Daniel Johannes, Al-Benna Sammy, Hauser Joerg, Ring Andrej, Steinstraesser Lars, Daigeler Adrien, Schmitz Inge, Steinau Hans Ulrich, Stricker Ingo

机构信息

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

Institute of Pathology, BG University Hospital Bergmannsheil, Ruhr University Bochum, Buerkle-de-la-Camp-Platz 1, 44789 Bochum, North Rhine-Westphalia, Germany.

出版信息

World J Oncol. 2012 Apr;3(2):47-53. doi: 10.4021/wjon496w. Epub 2012 Apr 23.

Abstract

BACKGROUND

The preclinical development of anti-sarcoma drugs has been primarily based on the subcutaneous transplantation of xenografts. Transplant survival remains an obstacle of current models which has been attributed to the period of hypoxia after transplantation. We hypothesized that primary soft tissue sarcoma models with an intrinsic tissue engineered vascular supply would be easily reproducible. The aim of this study was to establish a model of primary human soft tissue sarcoma with an intrinsic vascular supply.

METHODS

Primary soft tissue sarcoma cells from resected human liposarcomas isolated and divided into tumour fragments were transplanted into a silicon chamber, placed around the superficial epigastric vessels in mice. Sarcoma xenograft samples were analysed histomorphologically (light/electron microscopy and immunohistochemistry).

RESULTS

All primary soft tissue sarcoma transplants engrafted, leading to solid tumours within 3 weeks. Histological and immunohistochemical staining confirmed the mouse xenografts as identical high grade liposarcomas compared to original tumour tissue.

CONCLUSION

This study established a reproducible xenograft model of primary human liposarcoma. This animal model could be of high value for studying human soft tissue sarcomas and their therapy.

摘要

背景

抗肉瘤药物的临床前开发主要基于异种移植瘤的皮下移植。移植瘤的存活仍然是当前模型的一个障碍,这归因于移植后的缺氧期。我们假设具有内在组织工程血管供应的原发性软组织肉瘤模型将易于复制。本研究的目的是建立一个具有内在血管供应的原发性人类软组织肉瘤模型。

方法

从切除的人脂肪肉瘤中分离出原发性软组织肉瘤细胞,将其分成肿瘤碎片,移植到置于小鼠腹壁浅血管周围的硅室中。对肉瘤异种移植样本进行组织形态学分析(光镜/电镜和免疫组织化学)。

结果

所有原发性软组织肉瘤移植均成功植入,3周内形成实体瘤。组织学和免疫组织化学染色证实,与原始肿瘤组织相比,小鼠异种移植瘤为相同的高级别脂肪肉瘤。

结论

本研究建立了一种可重复的原发性人类脂肪肉瘤异种移植模型。该动物模型对于研究人类软组织肉瘤及其治疗可能具有很高的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0a/5649888/36cfc8d9ffc3/wjon-03-047-g001.jpg

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