Evidence map›Paper›PMID 31519914›Full record

ArticleNature communications2019

Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making.

Matthew R Zanotelli, Aniqua Rahman-Zaman, Jacob A VanderBurgh, Paul V Taufalele, Aadhar Jain, David Erickson, Francois Bordeleau, Cynthia A Reinhart-King

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 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 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing 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

102 citing papers in PubMed.

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42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Matthew R ZanotelliNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.ORCID http://orcid.org/0000-0001-8547-6451
Aniqua Rahman-ZamanNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.
Jacob A VanderBurghNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.
Paul V TaufaleleDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Aadhar JainSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
David EricksonSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Francois BordeleauDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA. francois.bordeleau@crchudequebec.ulaval.ca.ORCID http://orcid.org/0000-0002-5114-1757
Cynthia A Reinhart-KingNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA. cynthia.reinhart-king@vanderbilt.edu.ORCID http://orcid.org/0000-0001-6959-3914

Funding

Molecular Determinants of Confined MigrationR01GM131178 · NIGMS · VANDERBILT UNIVERSITY · PI MARKOV, DMITRY · 2019 to 2022
$1.5M
NIGMS NIH HHS R01 GM131178
6 · The paper itself

Abstract

Cell migration during the invasion-metastasis cascade requires cancer cells to navigate a spatially complex microenvironment that presents directional choices to migrating cells. Here, we investigate cellular energetics during migration decision-making in confined spaces. Theoretical and experimental data show that energetic costs for migration through confined spaces are mediated by a balance between cell and matrix compliance as well as the degree of spatial confinement to direct decision-making. Energetic costs, driven by the cellular work needed to generate force for matrix displacement, increase with increasing cell stiffness, matrix stiffness, and degree of spatial confinement, limiting migration. By assessing energetic costs between possible migration paths, we can predict the probability of migration choice. Our findings indicate that motility in confined spaces imposes high energetic demands on migrating cells, and cells migrate in the direction of least confinement to minimize energetic costs. Therefore, therapeutically targeting metabolism may limit cancer cell migration and metastasis.

Indexed as

Decision MakingAdenosine DiphosphateAdenosine TriphosphateBiomedical EngineeringCaveolin 1Cell Line, TumorCell MovementGlucoseHumansMicroscopy, Atomic ForceMicroscopy, ConfocalMicroscopy, Phase-ContrastRNA, Small InterferingAdenosine DiphosphateAdenosine TriphosphateCaveolin 1GlucoseRNA, Small Interfering

Identifiers

PMID31519914
PMCPMC6744572

What OpenQuestion holds

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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.