Evidence map›Paper›PMID 34935305›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Therapeutic Potentials of Poly (ADP-Ribose) Polymerase 1 (PARP1) Inhibition in Multiple Sclerosis and Animal Models: Concept Revisiting.

Yan Wang, David Pleasure, Wenbin Deng, Fuzheng Guo

Open access · goldAbstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. 18β-Glycyrrhetinic Acid AttenuatesAnimals : an open access journal from MDPI · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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  10. Oligodendrocyte Maturation Alters the Cell Death Mechanisms That Cause Demyelination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Review
  12. SPOP Mutations Target STING1 Signaling in Prostate Cancer and Create Therapeutic Vulnerabilities to PARP Inhibitor-Induced Growth Suppression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  13. Review
  14. In Silico Drug Repurposing in Multiple Sclerosis Using scRNA-Seq Data.International journal of molecular sciences · 2023
    Article
  15. 18β-Glycyrrhetinic Acid AlleviatesInfection and drug resistance · 2023
    Article
  16. Review
  17. 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

4 authors at 2 institutions in 2 countries.

Yan WangDepartment of Neurology, School of Medicine, University of California, Davis, CA, 95817, USA.
David PleasureDepartment of Neurology, School of Medicine, University of California, Davis, CA, 95817, USA.
Wenbin DengSchool of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Guangzhou, 510006, China.
Fuzheng GuoDepartment of Neurology, School of Medicine, University of California, Davis, CA, 95817, USA.ORCID 0000-0003-3410-8389
Shriners Hospitals for Children - Erie · USSun Yat-sen University · CN

Funding

Glial HIFa: mechanisms and implications in hypoxia/ischemia-induced oligodendroglial pathologyR01NS123080 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GUO, FUZHENG · 2021 to 2025
$2.3M
The Wnt-independent role of TCF7l2 in CNS myelin formation and repairR01NS094559 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GUO, FUZHENG · 2016 to 2020
$1.4M
A paradigm shift in our understanding of oligodendroglial HIFa-regulated CNS angiogenesisR21NS109790 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GUO, FUZHENG · 2018 to 2019
$432k
Manipulating N-acetyl-L-aspartate to reverse Canavan leukodystrophyR21NS117386 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PLEASURE, DAVID E. · 2020 to 2020
$432k
Manipulating N-acetyl-L-aspartate transport to treat Canavan leukodystrophyR21NS126173 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PLEASURE, DAVID E. · 2022 to 2023
$432k
CANAVAN DISEASE: SUPPRESSING THE PHENOTYPE BY INHIBITING NAA SYNTHESISR21NS096004 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PLEASURE, DAVID E. · 2015 to 2016
$431k
NINDS NIH HHS R01 NS094559NINDS NIH HHS R01 NS123080NINDS NIH HHS R21 NS109790NINDS NIH HHS R21 NS117386NINDS NIH HHS R21 NS126173
6 · The paper itself

Abstract

Poly (ADP-ribose) polymerase 1 (PARP1) plays a fundamental role in DNA repair and gene expression. Excessive PARP1 hyperactivation, however, has been associated with cell death. PARP1 and/or its activity are dysregulated in the immune and central nervous system of multiple sclerosis (MS) patients and animal models. Pharmacological PARP1 inhibition is shown to be protective against immune activation and disease severity in MS animal models while genetic PARP1 deficiency studies reported discrepant results. The inconsistency suggests that the function of PARP1 and PARP1-mediated PARylation may be complex and context-dependent. The article reviews PARP1 functions, discusses experimental findings and possible interpretations of PARP1 in inflammation, neuronal/axonal degeneration, and oligodendrogliopathy, three major pathological components cooperatively determining MS disease course and neurological progression, and points out future research directions. Cell type specific PARP1 manipulations are necessary for revisiting the role of PARP1 in the three pathological components prior to moving PARP1 inhibition into clinical trials for MS therapy.

Indexed as

Multiple SclerosisPoly (ADP-Ribose) Polymerase-1AnimalsDNA RepairHumansPoly ADP RibosylationPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1demyelinationinflammatory demyelinating diseasemultiple sclerosisneuroinflammationneuronal/axonal degenerationPARP1poly-ADP ribosylation

Identifiers

PMID34935305
PMCPMC8844485
OpenAlexW4200018435

What OpenQuestion holds

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LicenceCC BY
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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.