Evidence map›Paper›PMID 26288350›Full record

ArticleThe Journal of investigative dermatology2015

Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene.

Carlos J Perez, Lars Mecklenburg, Jean Jaubert, Lucia Martinez-Santamaria, Brian M Iritani, Alexsandra Espejo, Eleonora Napoli, Gyu Song, Marcela Del Río, John DiGiovanni and 8 more

Abstract read
In one paragraph

Article in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. DNA Methylation-Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging.Clinical, cosmetic and investigational dermatology · 2025
    Article
  7. S-acylation of CaChronic diseases and translational medicine · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Insights into auto-RSC chemical biology · 2021
    Review
  13. Review
  14. The desmosome as a model for lipid raft driven membrane domain organization.Biochimica et biophysica acta. Biomembranes · 2020
    Review
  15. Article
  16. Review
  17. Review
  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

18 authors at 6 institutions in 3 countries.

Carlos J PerezDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA.
Lars MecklenburgMecklenburg-consulting, Hamburg, Germany.
Jean JaubertUnité de Génétique Fonctionnelle de la Souris, Institut Pasteur, Paris, France.
Lucia Martinez-SantamariaDepartment of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain; Regenerative Medicine Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain; Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.
Brian M IritaniThe Department of Comparative Medicine, University of Washington, Seattle, Washington, USA.
Alexsandra EspejoDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA.
Eleonora NapoliDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
Gyu SongDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, California, USA.
Marcela Del RíoDepartment of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain; Regenerative Medicine Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain; Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.
John DiGiovanniDell Pediatric Research Institute, University of Texas, Austin, Texas, USA.
Cecilia GiuliviDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, California, USA; Medical Investigations of Neurodevelopmental Disorders (M. I. N. D.) Institute, University of California Davis, Sacramento, California, USA.
Mark T BedfordDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA.
Sharon Y R DentDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA.
Richard D WoodDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA.
Donna F KusewittDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA.
Jean-Louis GuénetUnité de Génétique Fonctionnelle de la Souris, Institut Pasteur, Paris, France.
Claudio J ContiDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; Department of Bioengineering, Universidad Carlos III de Madrid, Madrid, Spain; Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.
Fernando BenavidesDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA. Electronic address: fbenavid@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USCentre for Biomedical Network Research on Rare Diseases · ESInstitut Pasteur · FRUniversity of California, Davis · USUniversity of California Davis Medical Center · USUniversity of Washington · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting Fnip1 to disrupt B cell development, metabolism, and transformationR01AI114556 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2015 to 2019
$2.0M
Function of REV3L in limiting oncogenesis via DNA damage toleranceR01CA132840 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WOOD, RICHARD D · 2009 to 2013
$1.6M
Folliculin Interacting Proteins in Lymphocyte Development and AutoimmunityR21AI109020 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2014 to 2015
$425k
Fnip1 Function in Lymphocyte Development, Activation and MetabolismR56AI092093 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2013 to 2013
$353k
Tecan EVO GenePaint robotS10OD016167 · OD · BAYLOR COLLEGE OF MEDICINE · PI LJUNGBERG, CECILIA · 2013 to 2013
$215k
NCI NIH HHS CA132840NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA132840NIAID NIH HHS R01 AI114556NIAID NIH HHS R21 AI109020NIAID NIH HHS R56 AI092093NIH HHS 1S10OD016167NIH HHS S10 OD016167
6 · The paper itself

Abstract

Here we describe a spontaneous mutation in the Zdhhc13 (zinc finger, DHHC domain containing 13) gene (also called Hip14l), one of 24 genes encoding palmitoyl acyltransferase (PAT) enzymes in the mouse. This mutation (Zdhhc13luc) was identified as a nonsense base substitution, which results in a premature stop codon that generates a truncated form of the ZDHHC13 protein, representing a potential loss-of-function allele. Homozygous Zdhhc13luc/Zdhhc13luc mice developed generalized hypotrichosis, associated with abnormal hair cycle, epidermal and sebaceous gland hyperplasia, hyperkeratosis, and increased epidermal thickness. Increased keratinocyte proliferation and accelerated transit from basal to more differentiated layers were observed in mutant compared with wild-type (WT) epidermis in untreated skin and after short-term 12-O-tetradecanoyl-phorbol-13-acetate treatment and acute UVB exposure. Interestingly, this epidermal phenotype was associated with constitutive activation of NF-κB (RelA) and increased neutrophil recruitment and elastase activity. Furthermore, tumor multiplicity and malignant progression of papillomas after chemical skin carcinogenesis were significantly higher in mutant mice than WT littermates. To our knowledge, this is the first report of a protective role for PAT in skin carcinogenesis.

Indexed as

Genetic Predisposition to DiseaseMutationAcyltransferasesAnimalsBromodeoxyuridineCodon, TerminatorEpidermal CellsKeratinocytesLeukocyte ElastaseMiceNeutrophil InfiltrationNF-kappa BNIH 3T3 CellsPhenotypeSkin NeoplasmsAcyltransferasesBromodeoxyuridineCodon, TerminatorLeukocyte ElastaseNF-kappa BZdhhc13 protein, mouse

Identifiers

PMID26288350
PMCPMC4898190
OpenAlexW1888854582

What OpenQuestion holds

Textmetadata
LicenceTDM
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.