Evidence map›Paper›PMID 26584160›Full record

ArticleLab on a chip2016

A high-throughput mechanofluidic screening platform for investigating tumor cell adhesion during metastasis.

A Spencer, C Spruell, S Nandi, M Wong, M Creixell, A B Baker

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Modular cone-and-plate device for mechanofluidic assays in Transwell inserts.Frontiers in bioengineering and biotechnology · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. 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

6 authors at 1 institution in 2 countries.

A SpencerDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com.
C SpruellDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com.
S NandiDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com.
M WongDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com.
M CreixellDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com.
A B BakerDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA. abbaker1@gmail.com and Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, TX, USA.
The University of Texas at Austin · US

Funding

Engineering Effective Revascularization Strategies for Ischemia in Disease StatesDP2OD008716 · OD · UNIVERSITY OF TEXAS AT AUSTIN · PI BAKER, AARON BLAIR · 2011 to 2011
$2.3M
NIH HHS 1DP2 OD008716-01NIH HHS DP2 OD008716
6 · The paper itself

Abstract

The metastatic spread of cancer is a major barrier to effective and curative therapies for cancer. During metastasis, tumor cells intravasate into the vascular system, survive in the shear forces and immunological environment of the circulation, and then extravasate into secondary tumor sites. Biophysical forces are potent regulators of cancer biology and are key in many of the steps of metastasis. In particular, the adhesion of circulating cells is highly dependent upon competing forces between cell adhesion receptors and the shear stresses due to fluid flow. Conventional in vitro assays for drug development and the mechanistic study of metastasis are often carried out in the absence of fluidic forces and, consequently, are poorly representative of the true biology of metastasis. Here, we present a novel high-throughput approach to studying cell adhesion under flow that uses a multi-well, mechanofluidic flow system to interrogate adhesion of cancer cell to endothelial cells, extracellular matrix and platelets under physiological shear stresses. We use this system to identify pathways and compounds that can potentially be used to inhibit cancer adhesion under flow by screening anti-inflammatory compounds, integrin inhibitors and a kinase inhibitor library. In particular, we identify several small molecule inhibitors of FLT-3 and AKT that are potent inhibitors of cancer cell adhesion to endothelial cells and platelets under flow. In addition, we found that many kinase inhibitors lead to increased adhesion of cancer cells in flow-based but not static assays. This finding suggests that even compounds that reduce cell proliferation might also enhance cancer cell adhesion during metastasis. Overall, our results validate a novel platform for investigating the mechanisms of cell adhesion under biophysical flow conditions and identify several potential inhibitors of cancer cell adhesion during metastasis.

Indexed as

High-Throughput Screening AssaysMicrofluidic Analytical TechniquesCell AdhesionCell ProliferationCells, CulturedHumansNeoplasm MetastasisStress, Mechanical

Identifiers

PMID26584160
PMCPMC4691538
OpenAlexW2140554183

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.