Evidence map›Paper›PMID 19644500›Full record

ArticleEMBO reports2009

ARF stimulates XPC to trigger nucleotide excision repair by regulating the repressor complex of E2F4.

Carmen Dominguez-Brauer, Yi-Ju Chen, Patrick M Brauer, Julia Pimkina, Pradip Raychaudhuri

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. SIRT7 promotes lung cancer progression by destabilizing the tumor suppressor ARF.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  2. Review
  3. Review
  4. Review
  5. GSK-3 promotes S-phase entry and progression inDevelopment (Cambridge, England) · 2018
    Article
  6. Article
  7. Review
  8. Review
  9. Article
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  11. Review
  12. Article
  13. Article
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  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Regulation of global genome nucleotide excision repair by SIRT1 through xeroderma pigmentosum C.Proceedings of the National Academy of Sciences of the United States of America · 2010
    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 1 country.

Carmen Dominguez-BrauerDepartment of Biochemistry and Molecular Genetics, University of Illinois, College of Medicine, M/C 669, 900 S. Ashland Avenue, Chicago, Illinois 60607, USA.
Yi-Ju Chen
Patrick M Brauer
Julia Pimkina
Pradip Raychaudhuri
University of Illinois Chicago · USFox Chase Cancer Center · US

Funding

Role of DDB in Checkpoint Control and CarcinogenesisR01CA077637 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 1999 to 2014
$3.6M
Mechanisms of Tumor Suppression by ARFR01CA100035 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 2004 to 2009
$1.5M
DNA damage response and DDBR01AG024138 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 2005 to 2009
$1.4M
NCI NIH HHS CA100035NCI NIH HHS CA100035SNCI NIH HHS CA 77637NCI NIH HHS R01 CA077637NCI NIH HHS R01 CA100035NIA NIH HHS AG 024138NIA NIH HHS R01 AG024138
6 · The paper itself

Abstract

The tumour suppressor ARF (alternative reading frame), which is mutated or silenced in various tumours, has a crucial role in tumour surveillance to suppress unwarranted cell growth and proliferation. ARF has also been linked to the DNA-damage-induced response of p53 because of its ability to inhibit murine double minute 2 (MDM2). Here, however, we provide genetic evidence for a role of ARF in nucleotide excision repair (NER) that is independent of p53. Cells lacking ARF are deficient in NER. Expression of ARF restores the repair activity, which coincides with increased expression of the damaged-DNA recognition protein xeroderma pigmentosum, complementation group C (XPC). We provide evidence that, by disrupting the interaction between E2F transcription factor 4 (E2F4) and DRTF polypeptide 1 (DP1), ARF reduces the interaction of the E2F4-p130 repressor complex with the promoter of XPC to ensure high-level expression of XPC. Together, our results point to an important 'care-taker'-type tumour-suppression function for ARF in NER through the increased expression of XPC.

Indexed as

DNA RepairAnimalsBase SequenceCell LineCyclin-Dependent Kinase Inhibitor p16DNADNA-Binding ProteinsE2F4 Transcription FactorGene Expression RegulationMiceMice, KnockoutProtein BindingProto-Oncogene Proteins c-mdm2Pyrimidine DimersTumor Suppressor Protein p53Cdkn2a protein, mouseCyclin-Dependent Kinase Inhibitor p16DNADNA-Binding ProteinsE2f4 protein, mouseE2F4 Transcription FactorMdm2 protein, mouseProto-Oncogene Proteins c-mdm2Pyrimidine DimersTumor Suppressor Protein p53Xpc protein, mouse

Identifiers

PMID19644500
PMCPMC2750060
OpenAlexW2053354529

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.