Evidence map›Paper›PMID 30670739›Full record

ArticleScientific reports2019

Quantitative phase imaging reveals matrix stiffness-dependent growth and migration of cancer cells.

Yanfen Li, Michael J Fanous, Kristopher A Kilian, Gabriel Popescu

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. Article
  3. Brillouin microscopy in cancer research: a review.Journal of biomedical optics · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yanfen Li *Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA.
Michael J Fanous *Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA.
Kristopher A KilianDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA. k.kilian@unsw.edu.au.ORCID http://orcid.org/0000-0002-8963-9796
Gabriel PopescuDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA. gpopescu@illinois.edu.ORCID http://orcid.org/0000-0002-8296-8095

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer progression involves complex signals within the tumor microenvironment that orchestrate proliferation and invasive processes. The mechanical properties of the extracellular matrix (ECM) within this microenvironment has been demonstrated to influence growth and the migratory phenotype that precedes invasion. Here we present the integration of a label-free quantitative phase imaging technique, spatial light interference microscopy (SLIM)-with protein-conjugated hydrogel substrates-to explore how the stiffness of the ECM influences melanoma cells of varying metastatic potential. Melanoma cells of high metastatic potential demonstrate increased growth and velocity characteristics relative to cells of low metastatic potential. Cell velocity in the highly metastatic population shows a relative insensitivity to matrix stiffness suggesting adoption of migratory routines that are independent of mechanics to facilitate invasion. The use of SLIM and engineered substrates provides a new approach to characterize the invasive properties of live cells as a function of microenvironment parameters. This work provides fundamental insight into the relationship between growth, migration and metastatic potential, and provides a new tool for profiling cancer cells for clinical grading and development of patient-specific therapeutic regimens.

Indexed as

AnimalsCell Line, TumorCell MovementDisease ProgressionExtracellular MatrixIntravital MicroscopyMiceNeoplasmsTumor Microenvironment

Identifiers

PMID30670739
PMCPMC6343033

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Registered trials

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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.