Evidence map›Paper›PMID 32497513›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2020

Exposed CendR Domain in Homing Peptide Yields Skin-Targeted Therapeutic in Epidermolysis Bullosa.

Toini Pemmari, Larisa Ivanova, Ulrike May, Prakash Lingasamy, Allan Tobi, Anja Pasternack, Stuart Prince, Olli Ritvos, Shreya Makkapati, Tambet Teesalu and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Fragile skin may benefit from decoration.Molecular therapy. Advances · 2026
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  4. Gene Therapy for Skin Aging.Current gene therapy · 2025
    Review
  5. Article
  6. Article
  7. Review
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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

13 authors at 5 institutions in 3 countries.

Toini PemmariFaculty of Medicine and Health Technology, Tampere University & Tampere University Hospital, 33520 Tampere, Finland.
Larisa IvanovaDepartment of Pediatrics, New York Medical College, Valhalla, NY 10595, USA.
Ulrike MayFaculty of Medicine and Health Technology, Tampere University & Tampere University Hospital, 33520 Tampere, Finland.
Prakash LingasamyLaboratory of Cancer Biology, Institute of Biomedicine and Translational Medicine, University of Tartu, 50411 Tartu, Estonia.
Allan TobiLaboratory of Cancer Biology, Institute of Biomedicine and Translational Medicine, University of Tartu, 50411 Tartu, Estonia.
Anja PasternackDepartment of Physiology, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland.
Stuart PrinceFaculty of Medicine and Health Technology, Tampere University & Tampere University Hospital, 33520 Tampere, Finland.
Olli RitvosDepartment of Physiology, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland.
Shreya MakkapatiDepartment of Pediatrics, New York Medical College, Valhalla, NY 10595, USA.
Tambet TeesaluLaboratory of Cancer Biology, Institute of Biomedicine and Translational Medicine, University of Tartu, 50411 Tartu, Estonia; Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA; Center for Nanomedicine, University of California, Santa Barbara, CA 93106, USA.
Mitchell S CairoDepartment of Pediatrics, New York Medical College, Valhalla, NY 10595, USA; Department of Microbiology and Immunology, New York Medical College, Valhalla, NY 10595, USA; Department of Pathology, New York Medical College, Valhalla, NY 10595, USA; Department of Medicine, New York Medical College, Valhalla, NY 10595, USA; Deparmtent of Cell Biology and Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Tero A H JärvinenFaculty of Medicine and Health Technology, Tampere University & Tampere University Hospital, 33520 Tampere, Finland. Electronic address: tero.jarvinen@tuni.fi.
Yanling LiaoDepartment of Pediatrics, New York Medical College, Valhalla, NY 10595, USA. Electronic address: yanling_liao@nymc.edu.
New York Medical College · USTampere University Hospital · FIUniversity of Helsinki · FIUniversity of Tartu · EEUniversity of California, Santa Barbara · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic skin-selective therapeutics would be a major advancement in the treatment of diseases affecting the entire skin, such as recessive dystrophic epidermolysis bullosa (RDEB), which is caused by mutations in the COL7A1 gene and manifests in transforming growth factor-β (TGF-β)-driven fibrosis and malignant transformation. Homing peptides containing a C-terminal R/KXXR/K motif (C-end rule [CendR] sequence) activate an extravasation and tissue penetration pathway for tumor-specific drug delivery. We have previously described a homing peptide CRKDKC (CRK) that contains a cryptic CendR motif and homes to angiogenic blood vessels in wounds and tumors, but it cannot penetrate cells or tissues. In this study, we demonstrate that removal of the cysteine from CRK to expose the CendR sequence confers the peptide novel ability to home to normal skin. Fusion of the truncated CRK (tCRK) peptide to the C terminus of an extracellular matrix protein decorin (DCN), a natural TGF-β inhibitor, resulted in a skin-homing therapeutic molecule (DCN-tCRK). Systemic DCN-tCRK administration in RDEB mice led to inhibition of TGF-β signaling in the skin and significant improvement in the survival of RDEB mice. These results suggest that DCN-tCRK has the potential to be utilized as a novel therapeutic compound for the treatment of dermatological diseases such as RDEB.

Indexed as

Protein Interaction Domains and MotifsAnimalsBiomarkersDisease Models, AnimalEpidermolysis BullosaFibrosisImmunohistochemistryMiceMice, KnockoutNeuropilin-1PeptidesProtein BindingRecombinant Fusion ProteinsSkinTransforming Growth Factor betaWound HealingBiomarkersNeuropilin-1PeptidesRecombinant Fusion ProteinsTransforming Growth Factor betacell penetrating peptideCendR sequencecollagen type VIIdecorinepidermolysis bullosaneuropilin-1NRP-1recombinant proteinskin woundTGF-βtransforming growth factor-βvascular homing peptide

Identifiers

PMID32497513
PMCPMC7403337
OpenAlexW3027722708

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.