CAFs and Cancer Cells Co-Migration in 3D Spheroid Invasion Assay

Methods Mol Biol. 2021:2179:243-256. doi: 10.1007/978-1-0716-0779-4_19.

Abstract

In many solid tumors, collective cell invasion prevails over single-cell dissemination strategies. Collective modes of invasion often display specific front/rear cellular organization, where invasive leader cells arise from cancer cell populations or the tumor stroma. Collective invasion involves coordinated cellular movements which require tight mechanical crosstalk through specific combinations of cell-cell interactions and cell-matrix adhesions. Cancer Associated Fibroblasts (CAFs) have been recently reported to drive the dissemination of epithelial cancer cells through ECM remodeling and direct intercellular contact. However, the cooperation between tumor and stromal cells remains poorly understood. Here we present a simple spheroid invasion assay to assess the role of CAFs in the collective migration of epithelial tumor cells. This method enables the characterization of 3D spheroid invasion patterns through live cell fluorescent labeling combined with spinning disc microscopy. When embedded in extracellular matrix, the invasive strands of spheroids can be tracked and leader/follower organization of CAFs and cancer cells can be quantified.

Keywords: 3D spheroid invasion; Cancer Associated Fibroblasts; Collective migration; Epithelial cancer cells; Leader/follower cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cancer-Associated Fibroblasts / cytology
  • Cancer-Associated Fibroblasts / physiology*
  • Cell Culture Techniques / methods
  • Cell Line, Tumor
  • Cell Movement*
  • Cell Tracking / instrumentation
  • Cell Tracking / methods*
  • Extracellular Matrix / chemistry
  • Humans
  • Imaging, Three-Dimensional / instrumentation
  • Imaging, Three-Dimensional / methods*
  • Microscopy, Fluorescence / instrumentation
  • Microscopy, Fluorescence / methods
  • Spheroids, Cellular / cytology
  • Spheroids, Cellular / physiology*
  • Tumor Cells, Cultured