Evidence map›Paper›PMID 26090614›Full record

ArticleOncotarget2015

Multifaceted role of TREX2 in the skin defense against UV-induced skin carcinogenesis.

Joan Manils, Diana Gómez, Mercè Salla-Martret, Heinz Fischer, Jason M Fye, Elena Marzo, Laura Marruecos, Inma Serrano, Rocío Salgado, Juan P Rodrigo and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. TREX1 as a Novel Immunotherapeutic Target.Frontiers in immunology · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. PostExcision Events in Human Nucleotide Excision Repair.Photochemistry and photobiology · 2017
    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

19 authors at 6 institutions in 3 countries.

Joan ManilsDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Diana GómezDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Mercè Salla-MartretDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Heinz FischerResearch Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Jason M FyeDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Elena MarzoDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Laura MarruecosDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Inma SerranoDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Rocío SalgadoDermatology Departament, Hospital del Mar, Barcelona, Spain.
Juan P RodrigoDepartment of Otolaryngology, Hospital Universitario Central de Asturias, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Juana M Garcia-PedreroDepartment of Otolaryngology, Hospital Universitario Central de Asturias, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Anna M SerafinPlataforma de Recerca Aplicada en Animal de Laboratori, Parc Científic de Barcelona, Barcelona, Spain.
Xavier CañasPlataforma de Recerca Aplicada en Animal de Laboratori, Parc Científic de Barcelona, Barcelona, Spain.
Carmen BenitoProtecció Radiològica, Universitat de Barcelona, Barcelona, Spain.
Agustí TollDermatology Departament, Hospital del Mar, Barcelona, Spain.
Sònia-Vanina ForcalesInstitute of Predictive and Personalized Medicine of Cancer, Badalona, Barcelona, Spain.
Fred W PerrinoDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Leopold EckhartResearch Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Concepció SolerDepartament de Patologia i Terapèutica Experimental, Facultat de Medicina, Campus de Bellvitge, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Universitat de Barcelona · ESHospital Del Mar · ESMedical University of Vienna · ATUniversidad de Oviedo · ESWake Forest University · USInstitute of Predictive and Personalized Medicine of Cancer · ES

Funding

Mechanisms of the 3'-5' deoxyribonucleasesR01GM069962 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PERRINO, FRED W · 2004 to 2012
$2.9M
NIGMS NIH HHS GM069962NIGMS NIH HHS R01 GM069962
6 · The paper itself

Abstract

TREX2 is a 3'-DNA exonuclease specifically expressed in keratinocytes. Here, we investigated the relevance and mechanisms of TREX2 in ultraviolet (UV)-induced skin carcinogenesis. TREX2 expression was up-regulated by chronic UV exposure whereas it was de-regulated or lost in human squamous cell carcinomas (SCCs). Moreover, we identified SNPs in the TREX2 gene that were more frequent in patients with head and neck SCCs than in healthy individuals. In mice, TREX2 deficiency led to enhanced susceptibility to UVB-induced skin carcinogenesis which was preceded by aberrant DNA damage removal and degradation as well as reduced inflammation. Specifically, TREX2 loss diminished the up-regulation of IL12 and IFNγ, key cytokines related to DNA repair and antitumor immunity. In UV-treated keratinocytes, TREX2 promoted DNA repair and passage to late apoptotic stages. Notably, TREX2 was recruited to low-density nuclear chromatin and micronuclei, where it interacted with phosphorylated H2AX histone, which is a critical player in both DNA repair and cell death. Altogether, our data provide new insights in the molecular mechanisms of TREX2 activity and establish cell autonomous and non-cell autonomous functions of TREX2 in the UVB-induced skin response.

Indexed as

AnimalsCarcinoma, Squamous CellDNA DamageExodeoxyribonucleasesFemaleHumansKeratinocytesMaleMiceMice, Inbred C57BLMice, KnockoutPhosphoproteinsSkin NeoplasmsUltraviolet RaysExodeoxyribonucleasesPhosphoproteinsTREX2 protein, humanDNA damageinflammationskin carcinogenesisTREX2UV radiation

Identifiers

PMID26090614
PMCPMC4673170
OpenAlexW1861850179

What OpenQuestion 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 OpenQuestion graph.