4.4 Article

Quantification of Breast Cancer Cell Invasiveness Using a Three-dimensional (3D) Model

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 88, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/51341

Keywords

Medicine; Issue 88; Breast cancer; cell invasion; extracellular matrix (ECM); three-dimensional (3D) cultures; immunocytochemistry; Matrigel; basement membrane matrix

Funding

  1. Canadian Institutes of Health Research (CIHR) [MOP 107972]
  2. CIHR New Investigator Salary Award
  3. Translational Breast Cancer Research Unit
  4. CIHR Strategic Training Program in Cancer Research and Technology Transfer, London Regional Cancer Program
  5. Translational Breast Cancer Research Unit, London Regional Cancer Program
  6. CIHR-Strategic Training Program in Cancer Research and Technology Transfer

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It is now well known that the cellular and tissue microenvironment are critical regulators influencing tumor initiation and progression. Moreover, the extracellular matrix (ECM) has been demonstrated to be a critical regulator of cell behavior in culture and homeostasis in vivo. The current approach of culturing cells on two-dimensional (2D), plastic surfaces results in the disturbance and loss of complex interactions between cells and their microenvironment. Through the use of three-dimensional (3D) culture assays, the conditions for cell-microenvironment interaction are established resembling the in vivo microenvironment. This article provides a detailed methodology to grow breast cancer cells in a 3D basement membrane protein matrix, exemplifying the potential of 3D culture in the assessment of cell invasion into the surrounding environment. In addition, we discuss how these 3D assays have the potential to examine the loss of signaling molecules that regulate epithelial morphology by immunostaining procedures. These studies aid to identify important mechanistic details into the processes regulating invasion, required for the spread of breast cancer.

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