Evidence map›Paper›PMID 41558676›Full record

ArticleACS biomaterials science & engineering2026

Ex Vivo Microfluidic Model Identifies a Role for Shear Stress during Ovarian Tumor Cell Attachment to Peritoneal Mesothelial Cells.

Vasilios A Morikis, Breanna Baker, Jillian A Martin, Angela Schab, Alessandra DiMauro, Gregory D Longmore, Whitney R Grither

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Vasilios A MorikisDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Breanna BakerDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.ORCID 0009-0001-7172-7384
Jillian A MartinDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Angela SchabDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Alessandra DiMauroDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Gregory D LongmoreDepartment of Medicine (Oncology), Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Whitney R GritherDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St. Louis, Missouri 63130, United States.ORCID 0000-0003-1053-6469

Funding

MOLECULAR ONCOLOGY TRAINING GRANTT32CA113275 · NCI · WASHINGTON UNIVERSITY · PI Matthew J Walter · 2006 to 2026
$5.7M
Leader cell development and function in Breast Tumor Collective MigrationR01CA254060 · NCI · WASHINGTON UNIVERSITY · PI Gregory D. Longmore, Amit Pathak · 2022 to 2026
$2.6M
Tumor stromal effects of DDR2 in metastasis regulationR01CA223758 · NCI · WASHINGTON UNIVERSITY · PI LONGMORE, GREGORY D. · 2018 to 2022
$1.9M
Chemo-Mechanical Feedback between CAFs, Leader Cells, and the Extracellular Microenvironment Regulates Leader Cell Regulated Collective Cell MigrationF32CA275212 · NCI · WASHINGTON UNIVERSITY · PI MORIKIS, VASILIOS ARIS · 2022 to 2022
$70k
Investigating tumor-mesothelial cell interactions during ovarian cancer metastasisF31CA271651 · NCI · WASHINGTON UNIVERSITY · PI SCHAB, ANGELA · 2023 to 2023
$24k
NCI NIH HHS F31 CA271651NCI NIH HHS F32 CA275212NCI NIH HHS R01 CA223758NCI NIH HHS R01 CA254060NCI NIH HHS T32 CA113275
6 · The paper itself

Abstract

Ascites, or a pathologic accumulation of intra-abdominal fluid, is a key feature of intraperitoneally disseminating cancers, such as ovarian cancer. This pathological fluid buildup can influence the adhesive abilities of ovarian cancer cells, as they spread throughout the abdominal cavity to form metastatic implants on organs lined with a specialized monolayer of mesothelial cells. Robust methods for assessing the impact of fluid shear stress on this cell-cell interaction are lacking. Here, we develop and characterize a novel microfluidic device that allows for the determination of the attachment of ovarian tumor cells to mesothelial cells under the influence of fluid flow. We show that the attachment of ovarian tumor cells to mesothelium is impacted by fluid shear stresses in a dynamic manner. We find that ovarian tumor cells secrete factor(s) that enhance the ability of ovarian tumor cells to more efficiently attach, and remain attached, to the mesothelium in the presence of fluid shear stress. This work advances the study of ovarian tumor cell metastasis, describing a robust method to screen and identify therapeutically targetable pathways of ovarian tumor cell-mesothelial cell intercommunication to potentially mitigate ovarian cancer progression.

Indexed as

Epithelial CellsMicrofluidicsOvarian NeoplasmsPeritoneumCell AdhesionCell Line, TumorEpitheliumFemaleHumansMicrofluidic Analytical TechniquesShear StrengthStress, Mechanicalmechanobiologymicrofluidicsovarian cancershear stress

Identifiers

PMID41558676
PMCPMC12900518

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.