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Updated: May 14, 2026

3D Cell-Printed Hypoxic Cancer-on-a-Chip for Recapitulating Pathologic Progression of Solid Cancer
Published on: January 5, 2021
HyPIC-3D enables characterization of migratory cancer cell subpopulations in 3D hypoxic microenvironments
Luana Schito1, Sergio Rey-Keim1
1UCD School of Medicine, Dublin 4, D04 C7X2, Ireland; UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4 D04 C7X2, Ireland.
Abstract:
Malignant tumors harbor cancer cell subpopulations with heterogeneous migratory behaviors. Identifying the molecular programs specifying whether these subpopulations migrate or remain stationary is essential for preventing metastasis and requires experimental approaches that directly separate and analyze these subpopulations as they move throughout 3D microenvironments. Here, we present "paired isolation and characterization in 3D hypoxic microenvironments" (HyPIC-3D), a method to isolate and characterize migratory and non-migratory cancer cell subpopulations from the same pool of spheroids. By adapting tissue culture inserts used for migration assays, we established a migration platform that preserves oxygen gradients and the spheroid architecture. HyPIC-3D shows that the pattern and extent of migration differ among cancer cell types while identifying distinct molecular switches and oxygen requirements underlying this heterogeneity. Integrated with image analysis tools, HyPIC-3D is implemented with standard computational and laboratory equipment and is amenable to diverse downstream applications, enabling mechanistic dissection of migration and discovery of metastatic regulators.
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