Source abstract
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.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States
Department of Bioengineering, Rice University, Houston, Texas 77030, United States
Center for Nanophase Materials Science, Oak Ridge National Laboratories, Knoxville, Tennessee 37830, United States
Vanderbilt Institute for Nanoscale Science and Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States
Department of Mechanical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States
Funding
National Cancer Institute