Abstract
During the metastatic cascade, cancer cells travel through the bloodstream as circulating tumor cells (CTCs) to a secondary site. Clustered CTCs have greater shear stress and treatment resistance, yet their biology remains poorly understood. We therefore engineered a tunable superhydrophobic array device (SHArD). The SHArD-C was applied to culture a clinically relevant model of CTC clusters. Using our device, we cultured a model of cancer cell aggregates of various sizes with immortalized cancer cell lines. These exhibited higher E-cadherin expression and are significantly more capable of surviving high fluid shear stress-related forces compared to single cells and model clusters grown using the control method, helping to explain why clustering may provide a metastatic advantage. Additionally, the SHArD-S, when compared with the AggreWell 800 method, provides a more consistent spheroid-forming device culturing reproducible sizes of spheroids for multiple cancer cell lines. Overall, we designed, fabricated, and validated an easily tunable engineered device which grows physiologically relevant three-dimensional (3D) cancer models containing tens to thousands of cells.
| Original language | English |
|---|---|
| Pages (from-to) | 23637-23654 |
| Number of pages | 18 |
| Journal | ACS Nano |
| Volume | 18 |
| Issue number | 34 |
| DOIs | |
| State | Published - Aug 27 2024 |
Funding
This work was funded by the National Institute of Health National Cancer Institute grant number CA203991.
Keywords
- 3D mammalian cell cultures
- biological-material interfaces
- cancer
- microfabrication
- nanostructured surfaces
- superhydrophobicity
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