Evidence map›Paper›PMID 25100319›Full record

ArticleJournal of the Royal Society, Interface2014

Mechanistic adaptability of cancer cells strongly affects anti-migratory drug efficacy.

Wei Sun, Chwee Teck Lim, Nicholas Agung Kurniawan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Proteinaceous Hydrogels for Bioengineering Advanced 3D Tumor Models.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Local extracellular matrix alignment directs cellular protrusion dynamics and migration through Rac1 and FAK.Integrative biology : quantitative biosciences from nano to macro · 2016
    Article
  17. Article
  18. 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

3 authors at 3 institutions in 2 countries.

Wei SunNUS Graduate School for Integrative Sciences and Engineering, Singapore 117456, Republic of Singapore.
Chwee Teck LimMechanobiology Institute, National University of Singapore, Singapore 117411, Republic of Singapore Department of Biomedical Engineering, National University of Singapore, Singapore 117576, Republic of Singapore Department of Mechanical Engineering, National University of Singapore, Singapore 117576, Republic of Singapore ctlim@nus.edu.sg.
Nicholas Agung KurniawanFOM Institute AMOLF, Science Park 104, 1098XG Amsterdam, The Netherlands kurniawan@amolf.nl.
Duke-NUS Medical School · SGInstitute for Atomic and Molecular Physics · NLNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer metastasis involves the dissemination of cancer cells from the primary tumour site and is responsible for the majority of solid tumour-related mortality. Screening of anti-metastasis drugs often includes functional assays that examine cancer cell invasion inside a three-dimensional hydrogel that mimics the extracellular matrix (ECM). Here, we built a mechanically tuneable collagen hydrogel model to recapitulate cancer spreading into heterogeneous tumour stroma and monitored the three-dimensional invasion of highly malignant breast cancer cells, MDA-MB-231. Migration assays were carried out in the presence and the absence of drugs affecting four typical molecular mechanisms involved in cell migration, as well as under five ECMs with different biophysical properties. Strikingly, the effects of the drugs were observed to vary strongly with matrix mechanics and microarchitecture, despite the little dependence of the inherent cancer cell migration on the ECM condition. Specifically, cytoskeletal contractility-targeting drugs reduced migration speed in sparse gels, whereas migration in dense gels was retarded effectively by inhibiting proteolysis. The results corroborate the ability of cancer cells to switch their multiple invasion mechanisms depending on ECM condition, thus suggesting the importance of factoring in the biophysical properties of the ECM in anti-metastasis drug screenings.

Indexed as

AmidesAntineoplastic AgentsBreast NeoplasmsCell MovementCytochalasin DDipeptidesExtracellular MatrixFemaleHumansHydrogel, Polyethylene Glycol DimethacrylateMicroscopy, ConfocalNeoplasm InvasivenessNeoplasm MetastasisNeoplastic Cells, CirculatingNocodazolePyridinesAmidesAntineoplastic AgentsCytochalasin DDipeptidesHydrogel, Polyethylene Glycol DimethacrylateN-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamideNocodazolePyridinesY 27632cancer metastasisdrug assayextracellular matrix mechanicsthree-dimensional cell migration

Identifiers

PMID25100319
PMCPMC4233748
OpenAlexW2082493039

What OpenQuestion holds

Textmetadata
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.