Evidence map›Paper›PMID 40899692›Full record

ReviewFASEB journal : official publication of the Federation of American Societies for Experimental Biology2025

The Pathophysiological Functions of Heparanases: From Evolution, Structural and Tissue-Specific Perspectives.

Elham Vahdatahar, Clément Daviaud, Hugo Main, Rachel Havret, Claire Debarnot, Laure Favot-Laforge, Jean-François Jégou, Ingrid Fruitier-Arnaudin, Antoine Dufour, Romain Vivès and 3 more

Abstract readReview
In one paragraph

Review in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. The Pathophysiological Functions of Heparanases: From Evolution, Structural and Tissue-Specific Perspectives.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    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

13 authors.

Elham VahdataharAix-Marseille Univ, CNRS, AFMB, Marseille, France.
Clément DaviaudLIENSs UMR 7266, CNRS-La Rochelle Université, La Rochelle, France.
Hugo MainLIENSs UMR 7266, CNRS-La Rochelle Université, La Rochelle, France.
Rachel HavretLIENSs UMR 7266, CNRS-La Rochelle Université, La Rochelle, France.
Claire DebarnotAix-Marseille Univ, CNRS, AFMB, Marseille, France.
Laure Favot-LaforgeUniversité de Poitiers, LITEC, UR15560, Poitiers, France.
Jean-François JégouUniversité de Poitiers, LITEC, UR15560, Poitiers, France.
Ingrid Fruitier-ArnaudinLIENSs UMR 7266, CNRS-La Rochelle Université, La Rochelle, France.
Antoine DufourDepartment of Physiology and Pharmacology, McCaig Institute for Bone and Joint Health, Hotchkiss Brain Institute, Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Romain VivèsUniversity of Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.
Franck MorelUniversité de Poitiers, LITEC, UR15560, Poitiers, France.
Yves BourneAix-Marseille Univ, CNRS, AFMB, Marseille, France.
Kévin BarangerLIENSs UMR 7266, CNRS-La Rochelle Université, La Rochelle, France.ORCID https://orcid.org/0000-0001-8206-8874

Funding

Agence Nationale de la Recherche (ANR) ANR-15-IDEX-02Agence Nationale de la Recherche (ANR) ANR-21-CE29-0022Agence Nationale de la Recherche (ANR) ANR-21-CE44-0004Agence Nationale de la Recherche (ANR) ANR-22-CE15-0041Aix-Marseille Université (AMU)Canadian Government | Natural Sciences and Engineering Research Council of Canada (NSERC) DGECR-2019-00112Conseil Régional Aquitaine (Région Nouvelle-Aquitaine)French Infrastructure for Integrated Structural Biology (FRISBI) ANR-10-INBS-0005La Rochelle Université (ULR)Ligue Contre le Cancer (French League Against Cancer)Université de Poitiers (UP)
6 · The paper itself

Abstract

Heparanase 1 (HPSE1) is a unique endoglycosidase responsible for the enzymatic cleavage of heparan sulfate, thereby playing important functions in cancer processes. In contrast, the structurally related Heparanase 2 (HPSE2) lacks catalytic activity and appears to counteract HPSE1 activities. However, contradictory observations in various pathologies highlight the need for a better understanding of the respective contributions of both heparanases. In this review, we provide a comprehensive resource about the biology of HPSE1 and HPSE2 based on findings from different mouse models, with an emphasis on immune cells and their involvement in skin pathophysiology. In addition, we explore the evolutionary relationships between the two heparanases and describe the structure-function of HPSE2 using the advanced protein-prediction tool AlphaFold 3 (AF3). These approaches unveil new insights for deciphering the functional molecular determinants that distinguish HPSE1 from HPSE2.

Indexed as

Evolution, MolecularGlucuronidaseAnimalsHeparanaseHeparan SulfateHumansMiceNeoplasmsGlucuronidaseHeparanaseHeparan SulfatecancerHeparanaseimmune cellmolecular modelingmouse modelskin inflammation

Identifiers

PMID40899692
PMCPMC12406646

What Socratic 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 Socratic graph.