Evidence map›Paper›PMID 31201850›Full record

ReviewFree radical biology & medicine2019

Interrogating Parkinson's disease associated redox targets: Potential application of CRISPR editing.

M A Artyukhova, Y Y Tyurina, C T Chu, T M Zharikova, H Bayır, V E Kagan, P S Timashev

Abstract readReview
In one paragraph

Review in Free radical biology & medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
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  11. SARS-CoV2 infectivity is potentially modulated by host redox status.Computational and structural biotechnology journal · 2020
    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

7 authors.

M A ArtyukhovaDepartment of Advanced Biomaterials, Institute for Regenerative Medicine, I.M. Sechenov First Moscow State Medical University, Russian Federation.
Y Y TyurinaCenter for Free Radical and Antioxidant Health, Department of Environmental Health, University of Pittsburgh, USA.
C T ChuDepartment of Pathology, Division of Neuropathology, University of Pittsburgh School of Medicine, Pittsburgh, USA.
T M ZharikovaDepartment of Advanced Biomaterials, Institute for Regenerative Medicine, I.M. Sechenov First Moscow State Medical University, Russian Federation; Institute for Urology and Reproductive Health, I.M. Sechenov First Moscow State Medical University, Russian Federation.
H BayırCenter for Free Radical and Antioxidant Health, Department of Environmental Health, University of Pittsburgh, USA; Department of Critical Care Medicine, University of Pittsburgh, USA.
V E KaganCenter for Free Radical and Antioxidant Health, Department of Environmental Health, University of Pittsburgh, USA; Laboratory of Navigational Redox Lipidomics and Department of Human Pathology, I.M. Sechenov Moscow State Medical University, Russian Federation; Department of Chemistry, University of Pittsburgh, USA; Department of Pharmacology and Chemical Biology, University of Pittsburgh, USA; Department of Radiation Oncology, University of Pittsburgh, USA. Electronic address: kagan@pitt.edu.
P S TimashevDepartment of Advanced Biomaterials, Institute for Regenerative Medicine, I.M. Sechenov First Moscow State Medical University, Russian Federation; Department of Polymers and Composites, N.N.Semenov Institute of Chemical Physics, Russian Federation; Institute of Photonic Technologies, Research Center "Crystallography and Photonics", Russian Academy of Sciences, Russian Federation.

Funding

Training and EducationU19AI068021 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GREENBERGER, JOEL S · 2005 to 2019
$44.4M
Regulation of Cardiolin Byosynthesis in Epithelial InjuryP01HL114453 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MALLAMPALLI, RAMA K · 2014 to 2023
$21.3M
Mapping Lipid Oxidation in Traumatic Brain Injury by Mass Spectrometric ImagingR01NS076511 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Hülya Bayir, Valerian E Kagan · 2012 to 2026
$6.8M
Regulation of Autophagy & Mitochondrial Recycling in Neuronal Cell Death- SupplementR01AG026389 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, CHARLEEN T · 2007 to 2024
$6.0M
Dendrite regulation by the mitochondrial kinase PINK1: Implications for PD/LBD Diversity SupplementR01NS101628 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Charleen T Chu, Zachary P Wills · 2017 to 2026
$4.0M
Lipids and Myeloid Cell Function in CancerR01CA165065 · NCI · WISTAR INSTITUTE · PI KAGAN, VALERIAN E, MONTANER, LUIS J · 2012 to 2022
$3.8M
Oxidative Lipidomics in Pediatric Traumatic Brain InjuryR01NS061817 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAYIR, HÜLYA · 2008 to 2018
$3.3M
LR-IL-22 for Mitigation and Management of Radiation InjuriesU01AI172885 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOEL S GREENBERGER · 2023 to 2026
$2.4M
Oxidative Lipidomics in Pediatric Traumatic Brain InjuryR37NS061817 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Hülya Bayir · 2021 to 2026
$2.2M
The molecular basis of cardiolipin-protein interactions implicated in intrinsic apoptosisR01GM113908 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAGAN, VALERIAN E · 2016 to 2019
$1.5M
NCI NIH HHS R01 CA165065NHLBI NIH HHS P01 HL114453NIAID NIH HHS U01 AI172885NIAID NIH HHS U19 AI068021NIA NIH HHS R01 AG026389NIGMS NIH HHS R01 GM113908NINDS NIH HHS R01 NS061817NINDS NIH HHS R01 NS076511NINDS NIH HHS R01 NS101628NINDS NIH HHS R37 NS061817
6 · The paper itself

Abstract

Loss of dopaminergic neurons in the substantia nigra is one of the pathogenic hallmarks of Parkinson's disease, yet the underlying molecular mechanisms remain enigmatic. While aberrant redox metabolism strongly associated with iron dysregulation and accumulation of dysfunctional mitochondria is considered as one of the major contributors to neurodegeneration and death of dopaminergic cells, the specific anomalies in the molecular machinery and pathways leading to the PD development and progression have not been identified. The high efficiency and relative simplicity of a new genome editing tool, CRISPR/Cas9, make its applications attractive for deciphering molecular changes driving PD-related impairments of redox metabolism and lipid peroxidation in relation to mishandling of iron, aggregation and oligomerization of alpha-synuclein and mitochondrial injury as well as in mechanisms of mitophagy and programs of regulated cell death (apoptosis and ferroptosis). These insights into the mechanisms of PD pathology may be used for the identification of new targets for therapeutic interventions and innovative approaches to genome editing, including CRISPR/Cas9.

Indexed as

CRISPR-Cas Systemsalpha-SynucleinCardiolipinsCRISPR-Associated Protein 9Dopaminergic NeuronsFerroptosisGene EditingHumansIronLipid PeroxidationMitochondriaMitophagyMutationOxidation-ReductionParkinson DiseaseReactive Oxygen Speciesalpha-SynucleinCardiolipinsCRISPR-Associated Protein 9IronReactive Oxygen SpeciesSNCA protein, humanCRISPR/Cas9FerroptosisIronIron homeostasisLipid peroxidationMitochondrial dysfunctionMitophagyParkinson's diseaseReactive oxygen species (ROS)

Identifiers

PMID31201850
PMCPMC6832799

What OpenQuestion holds

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Registered trials

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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.