Evidence map›Paper›PMID 30567936›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2019

Poly(ADP-Ribose) Polymerases in Host-Pathogen Interactions, Inflammation, and Immunity.

Pamlea N Brady, Anupam Goel, Margaret A Johnson

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Oncology research · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Biomolecules & biomedicine · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Pathogenesis of Dementia.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Pamlea N BradyDepartment of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Anupam GoelCatalent Pharma Solutions, Philadelphia, Pennsylvania, USA.
Margaret A JohnsonDepartment of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA maggiejohnson@uab.edu.ORCID 0000-0002-4422-399X
University of Alabama at Birmingham · USCatalent (United States) · US

Funding

Mentored Experiences in Research, Instruction and Teaching (MERIT) Program - administrative supplementK12GM088010 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHNEIDER, DAVID ALAN · 2009 to 2024
$9.2M
Novel Nucleic Acid-Binding Proteins in Emerging VirusesR35GM119456 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JOHNSON, MARGARET ALICE · 2016 to 2018
$951k
NIGMS NIH HHS K12 GM088010NIGMS NIH HHS R35 GM119456
6 · The paper itself

Abstract

The literature review presented here details recent research involving members of the poly(ADP-ribose) polymerase (PARP) family of proteins. Among the 17 recognized members of the family, the human enzyme PARP1 is the most extensively studied, resulting in a number of known biological and metabolic roles. This review is focused on the roles played by PARP enzymes in host-pathogen interactions and in diseases with an associated inflammatory response. In mammalian cells, several PARPs have specific roles in the antiviral response; this is perhaps best illustrated by PARP13, also termed the zinc finger antiviral protein (ZAP). Plant stress responses and immunity are also regulated by poly(ADP-ribosyl)ation. PARPs promote inflammatory responses by stimulating proinflammatory signal transduction pathways that lead to the expression of cytokines and cell adhesion molecules. Hence, PARP inhibitors show promise in the treatment of inflammatory disorders and conditions with an inflammatory component, such as diabetes, arthritis, and stroke. These functions are correlated with the biophysical characteristics of PARP family enzymes. This work is important in providing a comprehensive understanding of the molecular basis of pathogenesis and host responses, as well as in the identification of inhibitors. This is important because the identification of inhibitors has been shown to be effective in arresting the progression of disease.

Indexed as

AnimalsDisease Models, AnimalHost-Pathogen InteractionsHumansImmunityInflammationPlantsPoly(ADP-ribose) PolymerasesProtein ConformationStress, PhysiologicalPoly(ADP-ribose) PolymerasesADP-ribosylationantiviral responsesautoimmunityenzyme inhibitionhost-pathogen interactionsinflammationpoly(ADP-ribose)poly(ADP-ribose) polymerasesstress granulestranscriptional regulation

Identifiers

PMID30567936
PMCPMC6383445
OpenAlexW2907558119

What Socratic 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 Socratic graph.