Evidence map›Paper›PMID 30991935›Full record

ReviewOpen biology2019

ADP-ribosylation signalling and human disease.

Luca Palazzo, Petra Mikolčević, Andreja Mikoč, Ivan Ahel

Open access · goldAbstract readReview
In one paragraph

Review in Open biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.6field-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

63 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Biomolecular NMR assignments · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Poly-ADP-ribosylation dynamics, signaling, and analysis.Environmental and molecular mutagenesis · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Decoding Ubiquitin Modifications by Mass Spectrometry.Advances in experimental medicine and biology · 2024
    Review
  20. A ribose-functionalized NADChemical communications (Cambridge, England) · 2023
    Article

3 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 3 countries.

Luca Palazzo1 Institute of Protein Biochemistry, National Research Council , Via Pietro Castellino 111, 80131 Naples , Italy.
Petra Mikolčević2 Division of Molecular Biology, Ruđer Bošković Institute , Bijenička cesta 54, 10000 Zagreb , Croatia.
Andreja Mikoč2 Division of Molecular Biology, Ruđer Bošković Institute , Bijenička cesta 54, 10000 Zagreb , Croatia.
Ivan Ahel3 Sir William Dunn School of Pathology, University of Oxford , South Parks Road, OX1 3RE Oxford , UK.
Ruđer Bošković Institute · HRInstitute of Protein Biochemistry · ITUniversity of Oxford · GB

Funding

Cancer Research UK 22284Cancer Research UK C35050/A22284Wellcome Trust 101794Wellcome Trust 210634
6 · The paper itself

Abstract

ADP-ribosylation (ADPr) is a reversible post-translational modification of proteins, which controls major cellular and biological processes, including DNA damage repair, cell proliferation and differentiation, metabolism, stress and immune responses. In order to maintain the cellular homeostasis, diverse ADP-ribosyl transferases and hydrolases are involved in the fine-tuning of ADPr systems. The control of ADPr network is vital, and dysregulation of enzymes involved in the regulation of ADPr signalling has been linked to a number of inherited and acquired human diseases, such as several neurological disorders and in cancer. Conversely, the therapeutic manipulation of ADPr has been shown to ameliorate several disorders in both human and animal models. These include cardiovascular, inflammatory, autoimmune and neurological disorders. Herein, we summarize the recent findings in the field of ADPr, which support the impact of this modification in human pathophysiology and highlight the curative potential of targeting ADPr for translational and molecular medicine.

Indexed as

ADP-RibosylationDNA RepairSignal TransductionADP Ribose TransferasesHumansModels, BiologicalNeoplasmsNervous System DiseasesProtein Processing, Post-TranslationalProteinsADP Ribose TransferasesProteinsADP-ribosylationsignallingtranslational medicine

Identifiers

PMID30991935
PMCPMC6501648
OpenAlexW2937494368

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.