Evidence map›Paper›PMID 24284422›Full record

ArticleThe Journal of investigative dermatology2014

Protein oxidation and DNA repair inhibition by 6-thioguanine and UVA radiation.

Quentin Gueranger, Feng Li, Matthew Peacock, Annabel Larnicol-Fery, Reto Brem, Peter Macpherson, Jean-Marc Egly, Peter Karran

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Influence of the Photodegradation of Azathioprine on DNA and Cells.International journal of molecular sciences · 2022
    Article
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  5. Review
  6. Article
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  10. Article
  11. Review
  12. Autophagy in UV Damage Response.Photochemistry and photobiology · 2017
    Review
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  15. Article
  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Quentin GuerangerCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.
Feng LiCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.
Matthew PeacockCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.
Annabel Larnicol-FeryInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/Inserm/ULP, BP163, Strasbourg, France.
Reto BremCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.
Peter MacphersonCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK.
Jean-Marc EglyInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/Inserm/ULP, BP163, Strasbourg, France.
Peter KarranCancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Herts, UK. Electronic address: peter.karran@cancer.org.uk.
Cancer Research UK · GBCentre National de la Recherche Scientifique · FRInserm · FR

Funding

Cancer Research UK 11584
6 · The paper itself

Abstract

Damage to skin DNA by solar UV is largely unavoidable, and an optimal cellular response to it requires the coordinated operation of proteins in numerous pathways. A fully functional DNA repair proteome for removing harmful DNA lesions is a prerequisite for an appropriate DNA damage response. Genetically determined failure to repair UV-induced DNA damage is associated with skin photosensitivity and increased skin cancer risk. Patients treated with immunosuppressant/anti-inflammatory thiopurines are also photosensitive and have high rates of sun-related skin cancer. Their DNA contains the base analog 6-thioguanine (6-TG), which acts as a UVA photosensitizer to generate reactive oxygen species (ROS), predominantly singlet oxygen ((1)O2). ROS damage both DNA and proteins. Here we show that UVA irradiation of cultured human cells containing DNA 6-TG causes significant protein oxidation and damages components of the DNA repair proteome, including the Ku, OGG-1, MYH, and RPA proteins. Assays of DNA repair in intact cells or in cell extracts indicate that this protein damage compromises DNA break rejoining and base and nucleotide excision repair. As these experimental conditions simulate those in the skin of patients taking thiopurines, our findings suggest a mechanism whereby UVA in sunlight may contribute to skin carcinogenesis in immunosuppressed patients.

Indexed as

AnimalsAnti-Inflammatory AgentsAntimetabolites, AntineoplasticCricetinaeDNA End-Joining RepairDNA GlycosylasesDNA HelicasesDNA RepairFibroblastsHeLa CellsHumansImmunosuppressive AgentsKu AutoantigenLeukemiaOxidation-ReductionPhotosensitivity DisordersAnti-Inflammatory AgentsAntimetabolites, AntineoplasticDNA GlycosylasesDNA HelicasesImmunosuppressive AgentsKu Autoantigenoxoguanine glycosylase 1, humanProteomeThioguanineXRCC5 protein, human

Identifiers

PMID24284422
OpenAlexW1989210919

What OpenQuestion holds

Textmetadata
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.