Evidence map›Paper›PMID 24800650›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2014

Modeling persistence in mesenchymal cell motility using explicit fibers.

David Lepzelter, Muhammad H Zaman

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Metalloproteinases in Ovarian Cancer.International journal of molecular sciences · 2021
    Review
  2. Article
  3. Review
  4. 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

2 authors.

David LepzelterDepartment of Biomedical Engineering, Boston University , Boston, Massachusetts 02215, United States.
Muhammad H Zaman

Funding

Modeling bi-directional signaling and cytoskeletal dynamics in 3D cell migrationsU01CA177799 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI GERTLER, FRANK B, KAMM, ROGER D · 2013 to 2017
$3.0M
NCI NIH HHS 1U01CA177799-01NCI NIH HHS U01 CA177799
6 · The paper itself

Abstract

Cell motility is central to a variety of fundamental processes ranging from cancer metastasis to immune responses, but it is still poorly understood in realistic native environments. Previous theoretical work has tended to focus on intracellular mechanisms or on small pieces of interaction with the environment. In this article, we present a simulation which accounts for mesenchymal movement in a 3D environment with explicit collagen fibers and show that this representation highlights the importance of both the concentration and alignment of fibers. We show good agreement with experimental results regarding cell motility and persistence in 3D environments and predict a specific effect on average instantaneous cell speed and persistence. Importantly, we show that a significant part of persistence in 3D is directly dependent on the physical environment, instead of indirectly dependent on the environment through the biochemical feedback that occurs in cell motility. Thus, new models of motility in three dimensions will need to account for the effects of explicit individual fibers on cells. This model can also be used to analyze cellular persistence in both mesenchymal and nonmesenchymal motility in complex three-dimensional environments to provide insights into mechanisms of cell motion seen in various cancer cell types in vivo.

Indexed as

Cell MovementExtracellular MatrixHumansMesenchymal Stem Cells

Identifiers

PMID24800650
PMCPMC4334298

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.