Evidence map›Paper›PMID 40833845›Full record

ArticleAmerican journal of physiology. Cell physiology2025

Aquaporin 5 expression regulates MDA-MB-231 spheroid multicellular invasion.

Ian M Smith, Autumn C Hengen, Ariel W Abraham, Sai Pranav Majeti Venkata, Shohini Banerjee, Nikka Givpoor, Allison K Moses, Kimberly M Stroka

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2025. 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

8 authors.

Ian M SmithFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.
Autumn C HengenFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.
Ariel W AbrahamFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.ORCID 0009-0009-9736-5121
Sai Pranav Majeti VenkataFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.ORCID 0009-0003-3250-6815
Shohini BanerjeeFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.ORCID 0000-0003-2331-6780
Nikka GivpoorFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.
Allison K MosesFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.
Kimberly M StrokaFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.ORCID 0000-0003-3314-2067

Funding

Exploring mechanisms of aquaporin-mediated cell migrationR35GM142838 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI STROKA, KIMBERLY · 2021 to 2025
$1.9M
HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM142838International Foundation for Ethical Research (IFER) Graduate FellowshipNIGMS NIH HHS R35 GM142838UMD | A. James Clark School of Engineering (Clark School of Engineering) Clark Doctoral Fellowship
6 · The paper itself

Abstract

Aquaporins are water transport proteins that regulate prometastatic behaviors in cancer, including cell invasion, proliferation, and epithelial-to-mesenchymal transition. Aquaporin 5, an isoform virtually absent from healthy tissues, is overexpressed in numerous cancer types. Studies have connected aquaporin 5 to the migratory and invasive properties of single cells in two-dimensional assays; however, the role of aquaporin 5 in inducing invasive phenotypes in models that recapitulate the tumor microenvironment remains unknown. To address this gap, MDA-MB-231 cell lines were created with aquaporin 5 overexpression and knockdown to identify the resulting single and collective cell motility in three-dimensional models. Upon validating the developed cell lines, aquaporin 5 expression regulated cell motility and invasion in varied biaxial microenvironments. In addition, aquaporin 5 was found to play a unique role in regulating MDA-MB-231 spheroid development, influencing the formation, size, circularity, and adhesion, distinct from its function in two-dimensional models. Finally, increased aquaporin 5 expression intensified the invasive capacity of spheroid multicellular protrusions by polarizing to their invasive front. In summary, this work expands upon the knowledge that aquaporin 5 enhances cell motility, while elucidating the previously unreported adhesive and multicellular invasive effects of aquaporin 5 in a three-dimensional model.

Indexed as

Aquaporin 5Breast NeoplasmsCell MovementSpheroids, CellularCell AdhesionCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessTumor MicroenvironmentAQP5 protein, humanAquaporin 5aquaporincell invasioncell motilityspheroid cohesionspheroid formation

Identifiers

PMID40833845
PMCPMC12422031

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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.