Evidence map›Paper›PMID 39150223›Full record

ArticleACS nano2024

Superhydrophobic Array Devices for the Enhanced Formation of 3D Cancer Models.

Maria Lopez-Cavestany, Olivia A Wright, Noah T Reckhorn, Alexandria T Carter, Kalana Jayawardana, Tin Nguyen, Dayrl P Briggs, Dmitry S Koktysh, Alberto Esteban Linares, Deyu Li and 1 more

Abstract read
In one paragraph

Article in ACS nano, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. The Application of 3D Cell Culture in Thyroid Cancer.Annals of biomedical engineering · 2026
    Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Maria Lopez-CavestanyDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Olivia A WrightDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Noah T ReckhornDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Alexandria T CarterDepartment of Bioengineering, Rice University, Houston, Texas 77030, United States.
Kalana JayawardanaDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Tin NguyenDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Dayrl P BriggsCenter for Nanophase Materials Science, Oak Ridge National Laboratories, Knoxville, Tennessee 37830, United States.
Dmitry S KoktyshVanderbilt Institute for Nanoscale Science and Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
Alberto Esteban LinaresDepartment of Mechanical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.ORCID 0000-0002-8637-2977
Deyu LiDepartment of Mechanical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.ORCID 0000-0001-8364-0924
Michael R KingDepartment of Bioengineering, Rice University, Houston, Texas 77030, United States.ORCID 0009-0006-4643-3663

Funding

Postdoctoral Training in Biomedical MRI and MRST32EB001628 · NIBIB · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John C Gore · 2003 to 2026
$7.0M
Super Natural Killer Cells That Target Metastases in the Tumor-Draining Lymph NodesR01CA203991 · NCI · VANDERBILT UNIVERSITY · PI KING, MICHAEL R. · 2017 to 2021
$1.9M
Enabling Technology to Study Mechanosensitive and Mechanoresistant Cancer Cells in FlowR01CA256054 · NCI · VANDERBILT UNIVERSITY · PI KING, MICHAEL R. · 2021 to 2025
$1.8M
NCI NIH HHS R01 CA203991NCI NIH HHS R01 CA256054NIBIB NIH HHS T32 EB001628
6 · The paper itself

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.

Indexed as

Hydrophobic and Hydrophilic InteractionsNeoplastic Cells, CirculatingCadherinsCell Culture TechniquesCell Line, TumorHumansSpheroids, CellularCadherins3D mammalian cell culturesbiological-material interfacescancermicrofabricationnanostructured surfacessuperhydrophobicity

Identifiers

PMID39150223
PMCPMC11363216

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.