Evidence map›Paper›PMID 37002342›Full record

ArticleBritish journal of cancer2023

A multimodal imaging study to highlight elastin-derived peptide pro-tumoral effect in a pancreatic xenograft model.

Lise Nannan, Willy Gsell, Sarah Belderbos, Célia Gallet, Jens Wouters, Sylvie Brassart-Pasco, Uwe Himmelreich, Bertrand Brassart

Abstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

8 authors.

Lise NannanKU Leuven, Department of Imaging and Pathology/Biomedical MRI, Leuven, Belgium.
Willy GsellKU Leuven, Department of Imaging and Pathology/Biomedical MRI, Leuven, Belgium.
Sarah BelderbosKU Leuven, Department of Imaging and Pathology/Biomedical MRI, Leuven, Belgium.
Célia GalletCNRS UMR 7369 Matrice Extracellulaire et Dynamique Cellulaire, Reims, France.
Jens WoutersKU Leuven, Department of Imaging and Pathology/Biomedical MRI, Leuven, Belgium.
Sylvie Brassart-PascoCNRS UMR 7369 Matrice Extracellulaire et Dynamique Cellulaire, Reims, France.
Uwe Himmelreich *KU Leuven, Department of Imaging and Pathology/Biomedical MRI, Leuven, Belgium.
Bertrand Brassart *CNRS UMR 7369 Matrice Extracellulaire et Dynamique Cellulaire, Reims, France. bertrand.brassart@univ-reims.fr.ORCID 0000-0002-4879-6832

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) is highly malignant with a very poor prognosis due to its silent development and metastatic profile with a 5-year survival rate below 10%. PDAC is characterised by an abundant desmoplastic stroma modulation that influences cancer development by extracellular matrix/cell interactions. Elastin is a key element of the extracellular matrix. Elastin degradation products (EDPs) regulate numerous biological processes such as cell proliferation, migration and invasion. The aim of the present study was to characterise for the first time the effect of two EDPs with consensus sequences "GxxPG" and "GxPGxGxG" (VG-6 and AG-9) on PDAC development. The ribosomal protein SA (RPSA) has been discovered recently, acting as a new receptor of EDPs on the surface of tumour cells, contributing to poor prognosis.

methodsSix week-old female Swiss nude nu/nu (Nu(Ico)-Foxn1

resultsAfter in vitro validation of MIA PaCa-2 cells by optical imaging, we demonstrated that EDPs exacerbate tumour growth in the PDAC mouse model. While VG-6 stimulated tumour growth to some extent, AG-9 had greater impact on tumour growth. We showed that the expression of the RPSA correlates with a possible effect of EDPs in the PDAC model. Multimodal imaging allowed for longitudinal in vivo follow-up of tumour development. In all groups, we showed mature vessels ending in close vicinity of the tumour, except for the AG-9 group where mature vessels are penetrating the tumour reflecting an increase of vascularisation.

conclusionsOur results suggest that AG-9 strongly increases PDAC progression through an increase in tumour vascularisation.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsCell Line, TumorCell ProliferationElastinFemaleHeterograftsHumansMiceMultimodal ImagingPeptidesElastinPeptides

Identifiers

PMID37002342
PMCPMC10206107

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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.