Evidence map›Paper›PMID 33780134›Full record

ArticleEMBO reports2021

Fibrotic enzymes modulate wound-induced skin tumorigenesis.

Lisette Van Hove, Kim Lecomte, Jana Roels, Niels Vandamme, Hanna-Kaisa Vikkula, Isabelle Hoorens, Katia Ongenae, Tino Hochepied, Giacomo Donati, Yvan Saeys and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Fibroblasts: invigorated targets in pre-metastatic niche formation.International journal of biological sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
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  12. 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

14 authors at 4 institutions in 4 countries.

Lisette Van HoveVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0002-4583-6923
Kim LecomteVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0001-8402-9799
Jana RoelsVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0001-6037-8767
Niels VandammeVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0001-6582-0040
Hanna-Kaisa VikkulaVIB Center for Inflammation Research, Ghent, Belgium.
Isabelle HoorensDepartment of Dermatology, University Hospital Ghent, Ghent, Belgium.
Katia OngenaeDepartment of Dermatology, University Hospital Ghent, Ghent, Belgium.
Tino HochepiedVIB Center for Inflammation Research, Ghent, Belgium.
Giacomo DonatiDepartment of Life Sciences and Systems Biology, Molecular Biotechnology Center, University of Turin, Turin, Italy.ORCID 0000-0002-0370-8288
Yvan SaeysVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0002-0415-1506
Sven R QuistDepartment of Dermatology and Venereology, Otto-von-Guericke University, Magdeburg, Germany.ORCID 0000-0002-9548-7813
Fiona M WattCentre for Stem Cells and Regenerative Medicine, King's College London, London, UK.ORCID 0000-0001-9151-5154
Geert van LooVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0002-8427-4775
Esther HosteVIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0002-3181-431X
Ghent University · BEKing's College London · GBGhent University Hospital · BEOtto-von-Guericke-Universität Magdeburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblasts are a major component of the microenvironment of most solid tumours. Recent research elucidated a large heterogeneity and plasticity of activated fibroblasts, indicating that their role in cancer initiation, growth and metastasis is complex and context-dependent. Here, we performed genome-wide expression analysis comparing fibroblasts in normal, inflammatory and tumour-associated skin. Cancer-associated fibroblasts (CAFs) exhibit a fibrotic gene signature in wound-induced tumours, demonstrating persistent extracellular matrix (ECM) remodelling within these tumours. A top upregulated gene in mouse CAFs encodes for PRSS35, a protease capable of collagen remodelling. In human skin, we observed PRSS35 expression uniquely in the stroma of high-grade squamous cell carcinomas. Ablation of PRSS35 in mouse models of wound- or chemically-induced tumorigenesis resulted in aberrant collagen composition in the ECM and increased tumour incidence. Our results indicate that fibrotic enzymes expressed by CAFs can regulate squamous tumour initiation by remodelling the ECM.

Indexed as

Extracellular MatrixFibroblastsAnimalsCarcinogenesisCell Transformation, NeoplasticFibrosisMiceSkinTumor Microenvironmentcancer-associated fibroblastsfibrosisPRSS35skin cancerwound healing

Identifiers

PMID33780134
PMCPMC8097359
OpenAlexW3142693906

What OpenQuestion holds

Textmetadata
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.