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一种独特的三维体外细胞侵袭试验。

A unique 3D in vitro cellular invasion assay.

作者信息

Quail Daniela F, Maciel Tamara J, Rogers Kem, Postovit Lynne M

机构信息

Western University, London, Ontario, Canada.

出版信息

J Biomol Screen. 2012 Sep;17(8):1088-95. doi: 10.1177/1087057112449863. Epub 2012 Jun 15.

Abstract

Three-dimensional (3D) cell culture techniques using a bioreactor have been used to co-culture various breast cancer cell lines. Comparisons between 3D co-cultures containing different proportions of breast cancer cell lines have been made with respect to cluster size, cell surface marker distribution, and Ki67 expression. Furthermore, an observed difference in invasion through collagen between co-cultures has been briefly reported. However, these assays have not yet been developed into a quantifiable methodology to assess the effects of drugs and/or microenvironments on cellular invasion. From a cancer perspective, two important aspects of cellular invasion that are often left out of in vitro assays are considerations about the 3D structural heterogeneity of the primary tumor and the ability of cells to migrate in all directions. Accordingly, we have taken advantage of the methodology previously described for 3D cell culture techniques and have developed a 3D invasion assay using cell clusters that can be used to assess the effects of different drugs and treatment conditions on cancer cell invasion. We also describe a novel whole-mount technique that permits fluorescence-based immunolocalization of proteins through the entire tumorsphere, without the need for sectioning. Our assay provides a simple, inexpensive, and physiologically relevant context to study cellular invasion in vitro, in a way that recapitulates an in vivo milieu.

摘要

使用生物反应器的三维(3D)细胞培养技术已被用于共培养各种乳腺癌细胞系。已对含有不同比例乳腺癌细胞系的3D共培养物在聚集体大小、细胞表面标志物分布和Ki67表达方面进行了比较。此外,还简要报道了共培养物之间在通过胶原蛋白侵袭方面观察到的差异。然而,这些检测方法尚未发展成为一种可量化的方法来评估药物和/或微环境对细胞侵袭的影响。从癌症的角度来看,体外检测中经常被忽略的细胞侵袭的两个重要方面是对原发性肿瘤三维结构异质性的考虑以及细胞向各个方向迁移的能力。因此,我们利用了先前描述的3D细胞培养技术方法,并开发了一种使用细胞聚集体的3D侵袭检测方法,可用于评估不同药物和治疗条件对癌细胞侵袭的影响。我们还描述了一种新颖的整装技术,该技术允许通过整个肿瘤球对蛋白质进行基于荧光的免疫定位,而无需切片。我们的检测方法提供了一种简单、廉价且与生理相关的体外研究细胞侵袭的环境,其方式可重现体内环境。

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