Evidence map›Paper›PMID 42236872›Full record

ArticleScientific reports2026

Mesenchymal transitions reduce lamin A expression and nuclear stiffness to enhance confined migration in glioblastoma.

Landon Teer, Neha Anil, Dominic Armagno, Bradley Mahaffey, Sihan Sun, Charles Froman-Glover, Akshitkumar Mistry, Kavitha Yaddanapudi, Joseph Chen

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Landon TeerDepartment of Bioengineering, University of Louisville, 2301 S. Third St, Lutz Hall 419, Louisville, KY, 40292, USA.
Neha AnilDepartment of Bioengineering, University of Louisville, 2301 S. Third St, Lutz Hall 419, Louisville, KY, 40292, USA.
Dominic ArmagnoDepartment of Bioengineering, University of Louisville, 2301 S. Third St, Lutz Hall 419, Louisville, KY, 40292, USA.
Bradley MahaffeyDepartment of Bioengineering, University of Louisville, 2301 S. Third St, Lutz Hall 419, Louisville, KY, 40292, USA.
Sihan SunDepartment of Biology, University of Louisville, Louisville, KY, USA.
Charles Froman-GloverDepartment of Medicine, University of Louisville, Louisville, KY, USA.
Akshitkumar MistryDepartment of Medicine, University of Louisville, Louisville, KY, USA.
Kavitha YaddanapudiUofL Health - Brown Cancer Center, University of Louisville, Louisville, KY, USA.
Joseph ChenDepartment of Bioengineering, University of Louisville, 2301 S. Third St, Lutz Hall 419, Louisville, KY, 40292, USA. joseph.chen@louisville.edu.

Funding

The role of ECM-mediated mechanosignaling on regional immunosuppression in GBMP20GM135004 · NIGMS · UNIVERSITY OF LOUISVILLE · PI JUN YAN · 2020 to 2026
$21.1M
NIGMS NIH HHS P20 GM135004NIH HHS P20GM135004
6 · The paper itself

Abstract

The evolution of glioblastoma (GBM) is coupled with a proneural-to-mesenchymal transition (PMT) that exacerbates disease in part through heightened cell invasiveness and spread. PMT follows similar molecular and phenotypic features with epithelial to mesenchymal transitions (EMT) and promotes rapid GBM invasion despite tight physical barriers in the dense brain parenchyma. Recent studies suggest that efficient confined migration is key to navigating these physical constraints; however, the role of PMT in mediating rapid confined migration remain unclear. Using microchannel platforms, AFM, and molecular assays, we explore this question through a biophysical lens to investigate the impact of GBM mesenchymal transformation on cellular mechanics and confined migration. We found that TGF-β1 induced PMT decreased expression and organization of Lamin A, leading to a reduction in nuclear stiffness, especially in U251 cells (1278 Pa → 682.6 Pa). Mesenchymal U251s migrated more quickly through confined microchannels though mesenchymal U87s migrated more slowly. Notably, nuclear stiffening via RO-3306 dramatically reduced confined migration speed in TGF-β1 treated U251 cells. Our study reveals that TGF-β1 induced PMT reduces Lamin A expression and softens the nucleus to support efficient confined migration in a cell-type dependent manner. These findings indicate that PMT alters the biophysical properties of the cell, opening new directions for developing therapeutic strategies for this deadly disease.

Indexed as

Brain NeoplasmsCell MovementCell NucleusEpithelial-Mesenchymal TransitionGlioblastomaLamin Type ACell Line, TumorGene Expression Regulation, NeoplasticHumansTransforming Growth Factor beta1Lamin Type ATransforming Growth Factor beta1Biophysical propertiesConfined migrationGlioblastomaNuclear mechanics

Identifiers

PMID42236872
PMCPMC13470200

What OpenQuestion holds

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Registered trials

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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.