Single cell and spheroid collagen type I invasion assay

  • Methods Mol Biol. 2014:1070:13-35. doi: 10.1007/978-1-4614-8244-4_2.
Olivier De Wever  1 An Hendrix Astrid De Boeck Frank Eertmans Wendy Westbroek Geert Braems Marc E Bracke
Affiliations
  • 1. Department of Radiotherapy and Nuclear Medicine, Laboratory of Experimental Cancer Research, Ghent University Hospital, Ghent, Belgium.
Abstract

Tumor invasion is the outcome of a complex interplay between Cancer cells and the stromal environment and requires the infiltration of a dense, cross-linked meshwork of Collagen type I extracellular matrix. We use a membrane-free single-cell and spheroid-based complementary model to study Cancer invasion through native Collagen type I matrices. Cell morphology is preserved during the assays allowing real-time monitoring of invasion-induced changes in cell structure and F-actin organization. Combination of these models with computerized quantification permits the calculation of highly reproducible and operator-independent data. These assays are versatile in the use of fluorescent probes and have a flexible kinetic endpoint. Once the optimal experimental conditions are empirically determined, the Collagen type I invasion assays can be used for preclinical validation of small-molecule inhibitors targeting invasion. Initiation and monitoring of the single-cell and spheroid invasion model can be achieved in 8 h (over 3 days) and in 14 h (over 5 days), respectively.