Evidence map›Paper›PMID 28531187›Full record

ArticlePLoS computational biology2017

Multi-scale computational study of the mechanical regulation of cell mitotic rounding in epithelia.

Ali Nematbakhsh, Wenzhao Sun, Pavel A Brodskiy, Aboutaleb Amiri, Cody Narciso, Zhiliang Xu, Jeremiah J Zartman, Mark Alber

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Cell division sets a universal flow geometry in cell layers.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  5. SEMAPL bioengineering · 2023
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  18. The Mechanics of Mitotic Cell Rounding.Frontiers in cell and developmental biology · 2020
    Review
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  20. Review
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

8 authors at 2 institutions in 1 country.

Ali NematbakhshDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, Indiana, United States of America.
Wenzhao SunDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, Indiana, United States of America.
Pavel A BrodskiyDepartment of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana, United States of America.
Aboutaleb AmiriDepartment of Physics, University of Notre Dame, Notre Dame, Indiana, United States of America.ORCID 0000-0001-7874-5123
Cody NarcisoDepartment of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana, United States of America.ORCID 0000-0002-4087-0241
Zhiliang XuDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, Indiana, United States of America.
Jeremiah J ZartmanDepartment of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana, United States of America.
Mark AlberDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, Indiana, United States of America.
University of Notre Dame · USUniversity of California, Riverside · US

Funding

Multiscale modeling and empirical study of a mechanism limiting blood clot growthU01HL116330 · NHLBI · UNIVERSITY OF NOTRE DAME · PI ALBER, MARK · 2014 to 2018
$3.5M
NHLBI NIH HHS U01 HL116330
6 · The paper itself

Abstract

Mitotic rounding during cell division is critical for preventing daughter cells from inheriting an abnormal number of chromosomes, a condition that occurs frequently in cancer cells. Cells must significantly expand their apical area and transition from a polygonal to circular apical shape to achieve robust mitotic rounding in epithelial tissues, which is where most cancers initiate. However, how cells mechanically regulate robust mitotic rounding within packed tissues is unknown. Here, we analyze mitotic rounding using a newly developed multi-scale subcellular element computational model that is calibrated using experimental data. Novel biologically relevant features of the model include separate representations of the sub-cellular components including the apical membrane and cytoplasm of the cell at the tissue scale level as well as detailed description of cell properties during mitotic rounding. Regression analysis of predictive model simulation results reveals the relative contributions of osmotic pressure, cell-cell adhesion and cortical stiffness to mitotic rounding. Mitotic area expansion is largely driven by regulation of cytoplasmic pressure. Surprisingly, mitotic shape roundness within physiological ranges is most sensitive to variation in cell-cell adhesivity and stiffness. An understanding of how perturbed mechanical properties impact mitotic rounding has important potential implications on, amongst others, how tumors progressively become more genetically unstable due to increased chromosomal aneuploidy and more aggressive.

Indexed as

AnimalsCell LineCell ShapeComputational BiologyDrosophilaEpithelial CellsHumansMitosisModels, Biological

Identifiers

PMID28531187
PMCPMC5460904
OpenAlexW2952599113

What OpenQuestion holds

Textmetadata
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.