Evidence map›Paper›PMID 31367506›Full record

ArticleEuropean physical journal plus2016

Epidermal growth factor promotes a mesenchymal over an amoeboid motility of MDA-MB-231 cells embedded within a 3D collagen matrix

Dongil T Geum, Beum Jun Kim, Audrey E Chang, Matthew S Hall, Mingming Wu

Open access · greenAbstract read
In one paragraph

Article in European physical journal plus, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Dongil T GeumDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
Beum Jun KimDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
Audrey E ChangResearch Apprenticeship in Biological Sciences, Cornell University, Ithaca, NY 14853, USA.
Matthew S HallDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
Mingming WuDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
Cornell University · US

Funding

TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
A 3D microfluidic platform for quantitative assessments of tumor cell migrationR21CA138366 · NCI · CORNELL UNIVERSITY · PI WU, MINGMING · 2010 to 2011
$347k
A 4D Traction Force Microscope for the mapping of cellular mechanical stressesR21RR025801 · NCRR · CORNELL UNIVERSITY · PI REINHART-KING, CYNTHIA A., WU, MINGMING · 2010 to 2011
$311k
NCI NIH HHS R21 CA138366NCI NIH HHS U54 CA143876NCRR NIH HHS R21 RR025801
6 · The paper itself

Abstract

The receptor of epidermal growth factor (EGFR) critically regulates tumor cell invasion and is a potent therapeutic target for treatment of many types of cancers, including carcinomas and glioblastomas. It is known that EGF regulates cell motility when tumor cells are embedded within a 3D biomatrix. However, roles of EGF in modulating tumor cell motility phenotype are largely unknown. In this article, we report that EGF promotes a mesenchymal over an amoeboid motility phenotype using a malignant breast tumor cell line, MDA-MB-231, embedded within a 3D collagen matrix. Amoeboid cells are rounded in shape, while mesenchymal cells are elongated, and their migrations are governed by a distinctly different set of biomolecules. Using single cell tracking analysis, we also show that EGF promotes cell dissemination through a significant increase in cell persistence along with a moderate increase of speed. The increase of persistence is correlated with the increase of the percentage of the mesenchymal cells within the population. Our work reveals a novel role of microenvironmental cue, EGF, in modulating heterogeneity and plasticity of tumor cell motility phenotype. In addition, it suggests a potential visual cue for diagnosing invasive states of breast cancer cells. This work can be easily extended beyond breast cancer cells.

Identifiers

PMID31367506
PMCPMC6668350
OpenAlexW2270566184

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.