Evidence map›Paper›PMID 32541776›Full record

ArticleScientific reports2020

Tumor spheroids under perfusion within a 3D microfluidic platform reveal critical roles of cell-cell adhesion in tumor invasion.

Yu Ling Huang, Yujie Ma, Cindy Wu, Carina Shiau, Jeffrey E Segall, Mingming Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Microphysiological systems for metastasis research: a stepwise approach.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  3. Review
  4. Article
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  6. A microfluidic rheometer for tumor mechanics and invasion studies.bioRxiv : the preprint server for biology · 2025
    Article
  7. Review
  8. Article
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  13. Article
  14. Modelling metastasis in a dish:Pathology oncology research : POR · 2025
    Review
  15. Article
  16. Article
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  18. Article
  19. Article
  20. Review
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 2 institutions in 1 country.

Yu Ling HuangDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, 14853, USA.
Yujie MaDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, 14853, USA.
Cindy WuDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, 14853, USA.
Carina ShiauDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, 14853, USA.
Jeffrey E SegallAnatomy and Structural Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, 10461, New York, USA.
Mingming WuDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, 14853, USA. mw272@cornell.edu.
Cornell University · USAlbert Einstein College of Medicine · US

Funding

TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
Microfluidic platform for tumor cell invasionR01CA221346 · NCI · CORNELL UNIVERSITY · PI Mingming Wu · 2017 to 2026
$3.4M
NCI NIH HHS R01 CA221346NCI NIH HHS U54 CA143876
6 · The paper itself

Abstract

Tumor invasion within the interstitial space is critically regulated by the force balance between cell-extracellular matrix (ECM) and cell-cell interactions. Interstitial flows (IFs) are present in both healthy and diseased tissues. However, the roles of IFs in modulating cell force balance and subsequently tumor invasion are understudied. In this article, we develop a microfluidic model in which tumor spheroids are embedded within 3D collagen matrices with well-defined IFs. Using co-cultured tumor spheroids (1:1 mixture of metastatic and non-tumorigenic epithelial cells), we show that IFs downregulate the cell-cell adhesion molecule E-cadherin on non-tumorigenic cells and promote tumor invasion. Our microfluidic model advances current tumor invasion assays towards a more physiologically realistic model using tumor spheroids instead of single cells under perfusion. We identify a novel mechanism by which IFs can promote tumor invasion through an influence on cell-cell adhesion within the tumor and highlight the importance of biophysical parameters in regulating tumor invasion.

Indexed as

Antigens, CDCadherinsCell AdhesionCell LineCoculture TechniquesCollagenDown-RegulationGene Expression Regulation, NeoplasticHumansMicrofluidic Analytical TechniquesNeoplasm InvasivenessSpheroids, CellularAntigens, CDCadherinsCDH1 protein, humanCollagen

Identifiers

PMID32541776
PMCPMC7295764
OpenAlexW3034314449

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.