Evidence map›Paper›PMID 39409898›Full record

ArticleCancers2024

Xeroderma Pigmentosum Type C Primary Skin Fibroblasts Overexpress HGF and Promote Squamous Cell Carcinoma Invasion in the Absence of Genotoxic Stress.

Sahar Al-Qaraghuli, Yannick Gache, Maria Goncalves-Maia, Damien Alcor, Elodie Muzotte, Walid Mahfouf, Hamid-Reza Rezvani, Thierry Magnaldo

Abstract read
In one paragraph

Article in Cancers, 2024. 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

8 authors.

Sahar Al-QaraghuliINSERM U1081-CNRS UMR7284-UNS, CEDEX 02, F-06107 Nice, France.
Yannick GacheINSERM U1081-CNRS UMR7284-UNS, CEDEX 02, F-06107 Nice, France.
Maria Goncalves-MaiaINSERM U1081-CNRS UMR7284-UNS, CEDEX 02, F-06107 Nice, France.
Damien AlcorFaculté de Médicine, 2ème étage, CNRS UMR 6267-INSERM U998-UNSA, F-06107 Nice Cedex 2, France.
Elodie MuzotteBRIC, UMR 1312, Inserm, Université de Bordeaux, F-33076 Bordeaux, France.
Walid MahfoufBRIC, UMR 1312, Inserm, Université de Bordeaux, F-33076 Bordeaux, France.
Hamid-Reza RezvaniBRIC, UMR 1312, Inserm, Université de Bordeaux, F-33076 Bordeaux, France.
Thierry MagnaldoINSERM U1081-CNRS UMR7284-UNS, CEDEX 02, F-06107 Nice, France.ORCID 0000-0001-9174-8599

Funding

Association pour la Recherche contre le Cancer ARC, SFI201212055859French Government (National Research Agency, ANR; CNRS; INSERM) through the 'Invest-ments for the Future' LABEX SIGNALIFE ANR-11-LABX-0028-01Société Française de Dermatologie n°174761, UMR7284
6 · The paper itself

Abstract

Xeroderma pigmentosum (XP) is a very rare recessive disease caused by the incapacity to resolve ultraviolet-induced DNA lesions through Nucleotide Excision Repair (NER). Most XP patients suffer from aggressive skin carcinoma and melanoma at a very early age (<8). Our previous results showed that primary XP fibroblasts isolated from healthy (non-photo-exposed) skin negatively impact the extracellular matrix and fail to activate the innate immune system. Here, we show for the first time that XP-C fibroblasts also play a major role in cancer cell invasion ex vivo and in vivo through the overexpression of Hepatocyte Growth Factor/Scatter Factor (HGF/SF) in the absence of genotoxic attacks. The use of inhibitors of the activation of the HGF/SF pathway counteracted the effects of XP fibroblasts on the growth of cancer cells, suggesting new perspectives in the care of XP patients.

Indexed as

fibroblastsHGF/SFsquamous cell carcinomaxeroderma pigmentosum

Identifiers

PMID39409898
PMCPMC11475422

What OpenQuestion holds

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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.