Evidence map›Paper›PMID 17724334›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Reprogramming of keratin biosynthesis by sulforaphane restores skin integrity in epidermolysis bullosa simplex.

Michelle L Kerns, Daryle DePianto, Albena T Dinkova-Kostova, Paul Talalay, Pierre A Coulombe

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03730649 (Effect of Topical Sulforaphane on Skin Aging and With Ultraviolet and Visible Light Exposure), which is not on this map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.7field-weighted citation impact, top 10% 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.

NCT03730649 early_phase1active not recruitingnot on this mapstarted 2019, after this paper: background citation

Effect of Topical Sulforaphane on Skin Aging and With Ultraviolet and Visible Light Exposure

TypeinterventionalSponsorJohns Hopkins UniversityRan2019 to 2026Enrolled12ConditionsSkin AgingArmsSulforaphane (broccoli sprout extract), UV or visible light
3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 93 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Intermediate filaments and their associated molecules.Journal of biomedical research · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Natural Nrf2 Modulators for Skin Protection.Antioxidants (Basel, Switzerland) · 2020
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 2 countries.

Michelle L KernsDepartment of Biological Chemistry, 725 North Wolfe Street, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Daryle DePianto
Albena T Dinkova-Kostova
Paul Talalay
Pierre A Coulombe
Laboratory of Molecular Genetics · PLJohns Hopkins Medicine · US

Funding

Non-Canonical Functions of Keratin Proteins in SkinR01AR044232 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COULOMBE, PIERRE · 1996 to 2020
$8.6M
TYPE II KERATIN GENES /PROTEINS IN COMPLEX EPITHELIAR01AR042047 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COULOMBE, PIERRE · 1995 to 2018
$7.1M
Role of Nrf2 Cross-Talk in Cancer ChemopreventionR01CA094076 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KENSLER, THOMAS W · 2002 to 2015
$5.5M
KERATIN INTERMEDIATE FILAMENTS AND SKIN DISEASESR55AR042047 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI COULOMBE, PIERRE · 1994 to 1994
–
NCI NIH HHS CA094076NCI NIH HHS R01 CA094076NIAMS NIH HHS AR42047NIAMS NIH HHS AR44232NIAMS NIH HHS R01 AR042047NIAMS NIH HHS R01 AR044232
6 · The paper itself

Abstract

Epidermolysis bullosa simplex (EBS) is a rare inherited condition in which the epidermis loses its integrity after mechanical trauma. EBS is typified by the dysfunction of intermediate filaments in basal keratinocytes of epidermis. Most cases of EBS are due to mutations in the keratin 5 or 14 gene (K5 and K14), whose products copolymerize to form intermediate filaments in basal keratinocytes. Available treatments for this disorder are only palliative. Here we exploit functional redundancy within the keratin gene family as the basis for therapy. We show that genetic activation of Gli2 or treatment with a pharmacological activator of Nrf2, two transcription factors eliciting distinct transcriptional programs, alleviates the blistering caused by a K14 deficiency in an EBS mouse model, correlating with K17 induction in basal epidermal keratinocytes. Nrf2 induction is brought about by treatment with sulforaphane, a natural product. Sulforaphane thus represents an attractive option for the prevention of skin blistering associated with K14 mutations in EBS.

Indexed as

AnimalsAnimals, NewbornBlisterEpidermolysis Bullosa SimplexGene Expression RegulationIsothiocyanatesKeratinsKruppel-Like Transcription FactorsMiceMice, TransgenicSulfoxidesThiocyanatesZinc Finger Protein Gli2Gli2 protein, mouseIsothiocyanatesKeratinsKruppel-Like Transcription FactorssulforaphaneSulfoxidesThiocyanatesZinc Finger Protein Gli2

Identifiers

PMID17724334
PMCPMC1964870
OpenAlexW2160596614

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.