Evidence map›Paper›PMID 41310721›Full record

ArticleJournal of experimental & clinical cancer research : CR2025

In vitro models to mimic tumor endothelial cell-mediated immune cell reprogramming in lung adenocarcinoma.

Morgane Krejbich, Emilie Navarro, Judith Fresquet, Marine Cotinat, Valentin Isen, Hortense Perdrieau, Virginie Forest, Aurélie Doméné, Tiphaine Delaunay, Hala Awada and 7 more

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 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. 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

17 authors.

Morgane KrejbichINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Emilie NavarroINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Judith FresquetINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Marine CotinatINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Valentin IsenHoneycomb team, Univ Rennes, UMR S1236, Rennes, France.
Hortense PerdrieauINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Virginie ForestCNRS, Inserm, l'institut du thorax, Nantes Université, CHU Nantes, Nantes, F-44000, France.
Aurélie DoménéCNRS, Inserm, BioCore, US16, SFR Bonamy, Nantes Université, CHU Nantes, Nantes, F-44000, France.
Tiphaine DelaunayINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Hala AwadaINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Vincent DochezService de Gynécologie-Obstétrique, INSERM, CIC 1413, Nantes Université, CHU Nantes, Nantes, F-44000, France.
David RouloisHoneycomb team, Univ Rennes, UMR S1236, Rennes, France.
Nicolas BoisgeraultINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Richard RedonCNRS, Inserm, l'institut du thorax, Nantes Université, CHU Nantes, Nantes, F-44000, France.
Christophe BlanquartINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Isabelle CorreINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France.
Lucas TrepsINSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d'Angers, Nantes, F-44000, France. lucas.treps@univ-nantes.fr.

Funding

Agence Nationale de la Recherche ANR-24-CE14-7852-01
6 · The paper itself

Abstract

Tumor endothelial cells (TECs) play a critical role in regulating immune responses within the tumor microenvironment (TME). However, the mechanisms by which TECs modulate immune cell population remain unclear, particularly in non-small cell lung cancer (NSCLC). Here, we investigated how NSCLC cells tweak normal endothelial cells (NECs) into TECs and the subsequent effects on immune regulation. NECs were cocultured with various NSCLC cell lines, using 2D and 3D coculture models to evaluate TEC-mediated effects on immune cells. We show that direct coculture led to significant transcriptomic, proteomic and kinomic alterations in TECs, especially in pro-inflammatory pathways. We identified a downregulation of the co-stimulatory molecule OX40L in TECs compared to NECs, suggesting impaired T-cell proliferation support. While TECs showed a limited effect on CD8

Indexed as

Adenocarcinoma of LungCellular ReprogrammingEndothelial CellsLung NeoplasmsCell Line, TumorCoculture TechniquesHumansTumor Microenvironment3D modelsCAFCancer-associated fibroblastImmunityMacrophagesNSCLCScRNA-seqSpheroidTumor endothelial cellsTumor microenvironment

Identifiers

PMID41310721
PMCPMC12817544

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.