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三维(3D)肿瘤球体侵袭试验。

Three-dimensional (3D) tumor spheroid invasion assay.

作者信息

Vinci Maria, Box Carol, Eccles Suzanne A

机构信息

Division of Molecular Pathology, The Institute of Cancer Research; Division of Cancer Therapeutics, The Institute of Cancer Research;

Division of Cancer Therapeutics, The Institute of Cancer Research.

出版信息

J Vis Exp. 2015 May 1(99):e52686. doi: 10.3791/52686.

DOI:10.3791/52686
PMID:25993495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4542056/
Abstract

Invasion of surrounding normal tissues is generally considered to be a key hallmark of malignant (as opposed to benign) tumors. For some cancers in particular (e.g., brain tumors such as glioblastoma multiforme and squamous cell carcinoma of the head and neck - SCCHN) it is a cause of severe morbidity and can be life-threatening even in the absence of distant metastases. In addition, cancers which have relapsed following treatment unfortunately often present with a more aggressive phenotype. Therefore, there is an opportunity to target the process of invasion to provide novel therapies that could be complementary to standard anti-proliferative agents. Until now, this strategy has been hampered by the lack of robust, reproducible assays suitable for a detailed analysis of invasion and for drug screening. Here we provide a simple micro-plate method (based on uniform, self-assembling 3D tumor spheroids) which has great potential for such studies. We exemplify the assay platform using a human glioblastoma cell line and also an SCCHN model where the development of resistance against targeted epidermal growth factor receptor (EGFR) inhibitors is associated with enhanced matrix-invasive potential. We also provide two alternative methods of semi-automated quantification: one using an imaging cytometer and a second which simply requires standard microscopy and image capture with digital image analysis.

摘要

侵袭周围正常组织通常被认为是恶性(与良性相对)肿瘤的一个关键特征。对于某些特定癌症(例如,多形性胶质母细胞瘤等脑肿瘤以及头颈部鳞状细胞癌——SCCHN)而言,它是导致严重发病的原因,甚至在没有远处转移的情况下也可能危及生命。此外,治疗后复发的癌症不幸的是往往表现出更具侵袭性的表型。因此,有机会针对侵袭过程提供新的疗法,这些疗法可以作为标准抗增殖药物的补充。到目前为止,由于缺乏适用于详细分析侵袭和药物筛选的强大、可重复的检测方法,这一策略受到了阻碍。在此,我们提供一种简单的微孔板方法(基于均匀、自组装的三维肿瘤球体),该方法在这类研究中具有巨大潜力。我们用人胶质母细胞瘤细胞系以及一个SCCHN模型来举例说明该检测平台,在这个SCCHN模型中,对靶向表皮生长因子受体(EGFR)抑制剂产生耐药性与增强的基质侵袭潜力相关。我们还提供了两种半自动定量的替代方法:一种使用成像细胞仪,另一种仅需要标准显微镜和带有数字图像分析的图像捕获。

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Tenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels.人神经胶质瘤中存在 tenascin-C 的表达,并与肿瘤血管有很强的相关性。
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