Multimodal Techniques to Study Tumor Growth, Basement Membrane Breaching, and Invasion in 3D Matrices
Publication date
2023
Editors
Margadant, C.
Advisors
Supervisors
Document Type
Part of book
Metadata
Show full item recordCollections
License
cc_by
Abstract
Cancer-derived organoids and three-dimensional (3D) extracellular matrix (ECM) are taking center stage as in vitro models to study neoplastic cell behavior, since they recapitulate the heterogeneous cellular composition of tumors and their extracellular environment. In combination with imaging and molecular/biochemical techniques, 3D organoid models have contributed substantially to our knowledge about the cellular and molecular mechanisms that regulate the growth of tumors and invasion into the surrounding tissue. We here outline a set of protocols that describe culturing of cancer-derived organoids in 3D matrices and various strategies that allow modeling of tumor growth, tumor cell penetration into basement membranes, and invasion into Collagen I-rich ECM. Furthermore, we specify protocols for subsequent handling of organoids cultured in 3D ECM for confocal microscopy and analysis of gene expression at the protein and mRNA level. Although we here use breast cancer-derived organoids, these protocols can be directly applied or adapted for organoids derived from other cancer types or healthy tissues. Thus, in addition to investigating cell behavior of multiple cancer types, the combination of protocols described here may be used to study processes such as cell differentiation and migration during homeostasis and normal development.
Keywords
3D cultures, Cancer cell invasion, Confocal microscopy, ECM remodeling, Extracellular matrix, Immunofluorescence, Organoids, Protein extraction, RNA extraction, Genetics, Molecular Biology
Citation
Smits, D & Khalil, A 2023, Multimodal Techniques to Study Tumor Growth, Basement Membrane Breaching, and Invasion in 3D Matrices. in C Margadant (ed.), Methods in Molecular Biology. Methods in Molecular Biology, vol. 2608, Humana New York, pp. 281–303. https://doi.org/10.1007/978-1-0716-2887-4_17