Evidence map›Paper›PMID 30595401›Full record

ReviewTrends in genetics : TIG2019

Multiple Roles for Mono- and Poly(ADP-Ribose) in Regulating Stress Responses.

Hongyun Qi, Brendan D Price, Tovah A Day

Open access · greenAbstract readReview
In one paragraph

Review in Trends in genetics : TIG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Prospects for PARG inhibitors in cancer therapy.Journal of molecular cell biology · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Large-scale proteomic analysis ofFrontiers in parasitology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. 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

3 authors at 2 institutions in 1 country.

Hongyun QiDepartment of Radiation Oncology, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA 02215, USA.
Brendan D PriceDepartment of Radiation Oncology, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA 02215, USA.
Tovah A DayDepartment of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA 02215, USA; Department of Biology, Clark University, 15 Maywood Street, Worcester, MA 01610, USA. Electronic address: tovah_day@dfci.harvard.edu.
Dana-Farber Cancer Institute · USClark University · US

Funding

RADIATION MODULATION OF THE P53 GENER01CA064585 · NCI · DANA-FARBER CANCER INSTITUTE · PI PRICE, BRENDAN D · 1995 to 2016
$4.6M
Nucleosome Dynamics and the Repair of DNA DamageR01CA177884 · NCI · DANA-FARBER CANCER INST · PI PRICE, BRENDAN D · 2013 to 2017
$1.8M
The Role of PARP3 in Telomere RegulationK01AG056554 · NIA · NORTHEASTERN UNIVERSITY · PI DAY, TOVAH · 2018 to 2022
$617k
NCI NIH HHS R01 CA064585NCI NIH HHS R01 CA177884NIA NIH HHS K01 AG056554
6 · The paper itself

Abstract

Although stress-induced synthesis of mono(ADP-ribose) (mADPr) and poly(ADP-ribose) (pADPr) conjugates by pADPr polymerase (PARP) enzymes has been studied extensively, the removal and degradation of pADPr, as well as the fate of ADPr metabolites, have received less attention. The observations that stress-induced pADPr undergoes rapid turnover, and that deficiencies in ADPr degradation phenocopy loss of pADPr synthesis, suggest that ADPr degradation is fundamentally important to the cellular stress response. Recent work has identified several distinct families of pADPr hydrolases that can degrade pADPr to release pADPr or mADPr into the cytoplasm. Further, many stress-response proteins contain ADPr-binding domains that can interact with these metabolites. We discuss how pADPr metabolites generated during pADPr degradation can function as signaling intermediates in processes such as inflammation, apoptosis, and DNA damage responses. These studies highlight that the full cycle of ADPr metabolism, including both synthesis and degradation, is necessary for responses to genotoxic stress.

Indexed as

ADP-RibosylationDNA DamagePoly Adenosine Diphosphate RiboseProtein DomainsProtein Processing, Post-TranslationalProteinsSignal TransductionStress, PhysiologicalPoly Adenosine Diphosphate RiboseProteins

Identifiers

PMID30595401
PMCPMC6338491
OpenAlexW2907934853

What OpenQuestion holds

Textmetadata
LicenceTDM
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.