Evidence map›Paper›PMID 34241907›Full record

ReviewJournal of neurochemistry2022

Emerging role of PARP-1 and PARthanatos in ischemic stroke.

Shuiqiao Liu, Weibo Luo, Yingfei Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of neurochemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Review
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  5. NADAlzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Non-canonical cell death in neurodegeneration: emerging mechanisms and therapeutic Frontiers.Apoptosis : an international journal on programmed cell death · 2026
    Review
  11. Review
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  13. Article
  14. Article
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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 1 institution in 1 country.

Shuiqiao LiuDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Weibo LuoDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Yingfei WangDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-8723-252X
The University of Texas Southwestern Medical Center · US

Funding

The role of AIF3 in neurodegeneration of Alzheimer's diseaseR01AG066166 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, YINGFEI · 2019 to 2023
$2.8M
PARP-1 Signaling in DNA Damage and Cell DeathR35GM124693 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, YINGFEI · 2017 to 2021
$2.0M
Role of SAP30 in hypoxia inducible factor activation and breast cancer progressionR01CA222393 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI LUO, WEIBO · 2019 to 2023
$1.8M
The role of a novel AIF-associated nuclease PAAN1 in neuronal injuryR00NS078049 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, YINGFEI · 2015 to 2017
$747k
The role of a novel AIF-associated nuclease PAAN1 in neuronal injuryK99NS078049 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WANG, YINGFEI · 2012 to 2013
$190k
NCI NIH HHS R01 CA222393NIA NIH HHS R01 AG066166NIGMS NIH HHS R35 GM124693NINDS NIH HHS K99 NS078049NINDS NIH HHS R00 NS078049
6 · The paper itself

Abstract

Cell death is a key feature of neurological diseases, including stroke and neurodegenerative disorders. Studies in a variety of ischemic/hypoxic mouse models demonstrate that poly(ADP-ribose) polymerase 1 (PARP-1)-dependent cell death, also named PARthanatos, plays a pivotal role in ischemic neuronal cell death and disease progress. PARthanatos has its unique triggers, processors, and executors that convey a highly orchestrated and programmed signaling cascade. In addition to its role in gene transcription, DNA damage repair, and energy homeostasis through PARylation of its various targets, PARP-1 activation in neuron and glia attributes to brain damage following ischemia/reperfusion. Pharmacological inhibition or genetic deletion of PARP-1 reduces infarct volume, eliminates inflammation, and improves recovery of neurological functions in stroke. Here, we reviewed the role of PARP-1 and PARthanatos in stroke and their therapeutic potential.

Indexed as

AnimalsHumansIschemic StrokeParthanatosPoly (ADP-Ribose) Polymerase-1Poly (ADP-Ribose) Polymerase-1NAD+oxidative stressPARP-1PARthanatosstroke

Identifiers

PMID34241907
PMCPMC9010225
OpenAlexW3178001607

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.