Evidence map›Paper›PMID 24169805›Full record

ArticleCellular and molecular life sciences : CMLS2014

Heparanase is preferentially expressed in human psoriatic lesions and induces development of psoriasiform skin inflammation in mice.

Immanuel Lerner, Eyal Zcharia, Tzahi Neuman, Esther Hermano, Ariel M Rubinstein, Israel Vlodavsky, Michael Elkin

Open access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. 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. Article
  5. Article
  6. Review
  7. Article
  8. The Role of Heparan Sulfate in Inflammation, and the Development of Biomimetics as Anti-Inflammatory Strategies.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2018
    Review
  9. Article
  10. Heparanase: From basic research to therapeutic applications in cancer and inflammation.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2016
    Review
  11. Article
  12. Impact of heparanase on renal fibrosis.Journal of translational medicine · 2015
    Review
  13. Article
  14. Article
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

7 authors at 2 institutions in 1 country.

Immanuel Lerner *Sharett Institute, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Eyal Zcharia *Sharett Institute, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Tzahi Neuman *Dept. of Pathology, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Esther HermanoSharett Institute, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Ariel M RubinsteinSharett Institute, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Israel VlodavskyCancer and Vascular Biology Research Center, The Rappaport Faculty of Medicine, Technion, Haifa 31096, Israel.
Michael ElkinSharett Institute, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Hadassah Medical Center · ILHebrew University of Jerusalem · IL

Funding

Regulation of heparanase in cancer progressionR01CA106456 · NCI · TECHNION-ISRAEL INSTITUTE OF TECHNOLOGY · PI VLODAVSKY, ISRAEL · 2004 to 2013
$1.7M
NCI NIH HHS R01 CA106456NCI NIH HHS R01-CA106456
6 · The paper itself

Abstract

Heparanase is the sole mammalian endoglycosidase that selectively degrades heparan sulfate, the key polysaccharide associated with the cell surface and extracellular matrix of a wide range of tissues. Extensively studied for its capacity to promote cancer progression, heparanase enzyme was recently implicated as an important determinant in several inflammatory disorders as well. Applying immunohistochemical staining, we detected preferential expression of heparanase by epidermal keratinocytes in human psoriatic lesions. To investigate the role of the enzyme in the pathogenesis of psoriasis, we utilized heparanase transgenic mice in a model of 12-O-tetradecanoyl phorbol 12-myristate 13-acetate-induced cutaneous inflammation. We report that over-expression of the enzyme promotes development of mouse skin lesions that strongly recapitulate the human disease in terms of histomorphological appearance and molecular/cellular characteristics. Importantly, heparanase of epidermal origin appears to facilitate abnormal activation of skin-infiltrating macrophages, thus generating psoriasis-like inflammation conditions, characterized by induction of STAT3, enhanced NF-κB signaling, elevated expression of TNF-α and increased vascularization. Taken together, our results reveal, for the first time, involvement of heparanase in the pathogenesis of psoriasis and highlight a role for the enzyme in facilitating abnormal interactions between immune and epithelial cell subsets of the affected skin. Heparanase inhibitors (currently under clinical testing in malignant diseases) could hence turn highly beneficial in psoriatic patients as well.

Indexed as

AnimalsCase-Control StudiesDermatitisGene Expression Regulation, EnzymologicGlucuronidaseHeparanaseHumansMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicPhenotypePsoriasisSkinGlucuronidaseHeparanase

Identifiers

PMID24169805
PMCPMC4059205
OpenAlexW1993507556

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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.