Evidence map›Paper›PMID 31302005›Full record

ReviewDNA repair2019

PARP-1 and its associated nucleases in DNA damage response.

Yijie Wang, Weibo Luo, Yingfei Wang

Open access · greenAbstract readReview
In one paragraph

Review in DNA repair, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 2% 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

130 citing papers in PubMed, 2 syntheses or guidelines pooled it, 251 citations in OpenAlex.

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  14. Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics.Apoptosis : an international journal on programmed cell death · 2026
    Review
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70 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

3 authors at 3 institutions in 1 country.

Yijie WangDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, 75390, USA.
Weibo LuoDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX, 75390, USA. Electronic address: Weibo.Luo@UTSouthwestern.edu.
Yingfei WangDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Neurology and Neurotherapeutics, UT Southwestern Medical Center, Dallas, TX, 75390, USA. Electronic address: Yingfei.Wang@UTSouthwestern.edu.
Southwestern Medical CenterSouthwestern Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

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
NCI NIH HHS R01 CA222393NIGMS NIH HHS R35 GM124693NINDS NIH HHS R00 NS078049
6 · The paper itself

Abstract

Poly(ADP-ribose) (PAR) polymerase-1 (PARP-1) acts as a DNA damage sensor. It recognizes DNA damage and facilitates DNA repair by recruiting DNA repair machinery to damage sites. Recent studies reported that PARP-1 also plays an important role in DNA replication by recognizing the unligated Okazaki fragments and controlling the speed of fork elongation. On the other hand, emerging evidence reveals that excessive activation of PARP-1 causes chromatin DNA fragmentation and triggers an intrinsic PARP-1-dependent cell death program designated parthanatos, which can be blocked by genetic deletion or pharmacological inhibition of PARP-1. Therefore, PARP-1 plays an essential role in maintaining genomic stability by either facilitating DNA repair/replication or triggering DNA fragmentation to kill cells. A group of structure-specific nucleases is crucial for executing DNA incision and fragmentation following PARP-1 activation. In this review, we will discuss how PARP-1 coordinates with its associated nucleases to maintain genomic integrity and control the decision of cell life and death.

Indexed as

DNA DamageDNA RepairAnimalsDNADNA ReplicationGenomic InstabilityHumansPoly (ADP-Ribose) Polymerase-1DNAPoly (ADP-Ribose) Polymerase-1Cell deathDNA damageDNA replication/repairNucleasePARP-1

Identifiers

PMID31302005
PMCPMC6764844
OpenAlexW2958031529

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.