Evidence map›Paper›PMID 40550569›Full record

ArticleJournal for immunotherapy of cancer2025

Melissa Bonner, David Askew, Vrishabhadev Sathish Kumar, Suzanne L Tomchuck, Saada Eid, Muta Abiff, Jay T Myers, Phuong Nguyen, Justin W A Garyu, Tyler E Miller and 1 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

11 authors.

Melissa BonnerDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
David AskewDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Vrishabhadev Sathish KumarDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Suzanne L TomchuckDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.ORCID http://orcid.org/0000-0002-4068-3470
Saada EidDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Muta AbiffDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Jay T MyersDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Phuong NguyenDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Justin W A GaryuDepartment of Medicine, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
Tyler E MillerDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.ORCID http://orcid.org/0000-0002-1269-1895
Alex Yee-Chen HuangDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA alex.y.huang@case.edu.ORCID http://orcid.org/0000-0002-5701-4521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor-associated myeloid cells (TAMCs) are an abundant, phenotypically plastic cell population that is critical for initiating a robust antitumor response. To properly combat cancer cells, TAMCs must sense and transduce both soluble and vital biophysical cues imparted by the dense extracellular matrix (ECM) of the tumor microenvironment (TME). Despite ample research enumerating the deleterious effects of a primary tumor's ECM on TAMCs' functionality, few studies have evaluated the contribution of mechanosensitive cation channel(s) underlying these detrimental changes.

methodsOur study aimed to evaluate the significance of the mechanosensitive cation channel PIEZO1 in TAMCs' phenotype and effector functionality. To do so, we generated CD11b-conditional

resultsGenetic deletion of

conclusionsHere, we report for the first time an association between mechanosensation and cross-presentation by cDC2A cells. Our findings may be impactful to improving the continued development of DC vaccines whose success hinges on proper antigen processing and presentation to cytotoxic T cells in the TME.

Indexed as

CD11b AntigenCD8-Positive T-LymphocytesCross-PrimingDendritic CellsIon ChannelsRhabdomyosarcomaAnimalsCell Line, TumorHumansMiceMice, KnockoutTumor MicroenvironmentCD11b AntigenIon ChannelsPiezo1 protein, mouseAntigen PresentationDendritic CellsMyeloidSolid tumorTumor Microenvironment

Identifiers

PMID40550569
PMCPMC12186042

What OpenQuestion holds

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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.