Evidence map›Paper›PMID 30958816›Full record

ArticlePLoS computational biology2019

Dynamic filopodial forces induce accumulation, damage, and plastic remodeling of 3D extracellular matrices.

Andrea Malandrino, Xavier Trepat, Roger D Kamm, Michael Mak

Abstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing 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

70 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Extracellular Matrix Viscoelasticity Regulates Mammary Branching Morphogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Deep learning reveals how cells pull, buckle, and navigate fibrous environments.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Cancer cell dynamics on silica fibers.Scientific reports · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Mechanical signatures in cancer metastasis.npj biological physics and mechanics · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

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

4 authors.

Andrea MalandrinoDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-7928-0951
Xavier TrepatInstitute for Bioengineering of Catalonia, Barcelona, Spain.
Roger D KammDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Michael MakYale University, Biomedical Engineering Department, New Haven, Connecticut, United States of America.ORCID 0000-0001-6881-8130

Funding

Research Supplement - Quantitative analyses of tumor cell extravasationU01CA202177 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2015 to 2020
$4.2M
Mechanical Self-Assembly of Dense Fibrotic Tumor Microenvironments: Mechanisms and TherapyR21EB026630 · NIBIB · YALE UNIVERSITY · PI MAK, MICHAEL · 2018 to 2020
$590k
NCI NIH HHS U01 CA202177NIBIB NIH HHS R21 EB026630
6 · The paper itself

Abstract

The mechanical properties of the extracellular matrix (ECM)-a complex, 3D, fibrillar scaffold of cells in physiological environments-modulate cell behavior and can drive tissue morphogenesis, regeneration, and disease progression. For simplicity, it is often convenient to assume these properties to be time-invariant. In living systems, however, cells dynamically remodel the ECM and create time-dependent local microenvironments. Here, we show how cell-generated contractile forces produce substantial irreversible changes to the density and architecture of physiologically relevant ECMs-collagen I and fibrin-in a matter of minutes. We measure the 3D deformation profiles of the ECM surrounding cancer and endothelial cells during stages when force generation is active or inactive. We further correlate these ECM measurements to both discrete fiber simulations that incorporate fiber crosslink unbinding kinetics and continuum-scale simulations that account for viscoplastic and damage features. Our findings further confirm that plasticity, as a mechanical law to capture remodeling in these networks, is fundamentally tied to material damage via force-driven unbinding of fiber crosslinks. These results characterize in a multiscale manner the dynamic nature of the mechanical environment of physiologically mimicking cell-in-gel systems.

Indexed as

Biomechanical PhenomenaBiopolymersCell LineCellular MicroenvironmentComputational BiologyComputer SimulationExtracellular MatrixHumansHuman Umbilical Vein Endothelial CellsImaging, Three-DimensionalKineticsModels, BiologicalPseudopodiaBiopolymers

Identifiers

PMID30958816
PMCPMC6472805

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.