Evidence map›Paper›PMID 35727353›Full record

ReviewArchives of toxicology2022

Ferroptosis as a mechanism of non-ferrous metal toxicity.

Michael Aschner, Anatoly V Skalny, Airton C Martins, Anton I Sinitskii, Marcelo Farina, Rongzhu Lu, Fernando Barbosa, Yordanka G Gluhcheva, Abel Santamaria, Alexey A Tinkov

Abstract readReview
PubMed Publisher
In one paragraph

Review in Archives of toxicology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 87 citations in OpenAlex.

  1. Salidroside in heavy metal toxicity: a mechanistic review of antioxidant, anti-inflammatory, and anti-apoptotic pathways.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
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  13. Metallic nanomedicine in cancer immunotherapy.Acta pharmaceutica Sinica. B · 2025
    Review
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  15. Article
  16. Ferroptosis in Toxicology: Present and Future.International journal of molecular sciences · 2025
    Review
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  18. Review
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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

10 authors at 8 institutions in 6 countries.

Michael Aschner *Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA. michael.aschner@einsteinmed.edu.ORCID 0000-0002-2619-1656
Anatoly V SkalnyWorld-Class Research Center "Digital Biodesign and Personalized Healthcare", IM Sechenov First Moscow State Medical University (Sechenov University), 119435, Moscow, Russia.
Airton C MartinsDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Anton I SinitskiiDepartment of Biochemistry, South Ural State Medical University, 453092, Chelyabinsk, Russia.
Marcelo FarinaDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, 88040-900, Brazil.
Rongzhu LuDepartment of Preventive Medicine and Public Health Laboratory Science, School of Medicine, Jiangsu University, 212013, Zhenjiang, Jiangsu, People's Republic of China.
Fernando BarbosaDepartment of Clinical Analyses, Toxicology and Food Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo-USP, Ribeirão Preto, Brazil.
Yordanka G GluhchevaDepartment of Experimental Morphology, Institute of Experimental Morphology, Pathology and Anthropology with Museum, Bulgarian Academy of Sciences, 1113, Sofia, Bulgaria.
Abel SantamariaLaboratorio de Aminoácidos Excitadores/Laboratorio de Neurofarmacología Molecular y Nanotecnología, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico.
Alexey A Tinkov *Laboratory of Molecular Dietetics, IM Sechenov First Moscow State Medical University (Sechenov University), 119435, Moscow, Russia.
Albert Einstein College of Medicine · USSechenov University · RUBulgarian Academy of Sciences · BGChelyabinsk State Medical Academy · RUInstituto Nacional de Neurología y Neurocirugía · MXJiangsu University · CNUniversidade de Ribeirão Preto · BRUniversidade Federal de Santa Catarina · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/24069-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/08139-4Russian Ministry of Science and Higher Education 0856-2020-0008
6 · The paper itself

Abstract

Ferroptosis is a recently discovered form of regulated cell death, implicated in multiple pathologies. Given that the toxicity elicited by some metals is linked to alterations in iron metabolism and induction of oxidative stress and lipid peroxidation, ferroptosis might be involved in such toxicity. Although direct evidence is insufficient, certain pioneering studies have demonstrated a crosstalk between metal toxicity and ferroptosis. Specifically, the mechanisms underlying metal-induced ferroptosis include induction of ferritinophagy, increased DMT-1 and TfR cellular iron uptake, mitochondrial dysfunction and mitochondrial reactive oxygen species (mitoROS) generation, inhibition of Xc-system and glutathione peroxidase 4 (GPX4) activity, altogether resulting in oxidative stress and lipid peroxidation. In addition, there is direct evidence of the role of ferroptosis in the toxicity of arsenic, cadmium, zinc, manganese, copper, and aluminum exposure. In contrast, findings on the impact of cobalt and nickel on ferroptosis are scant and nearly lacking altogether for mercury and especially lead. Other gaps in the field include limited studies on the role of metal speciation in ferroptosis and the critical cellular targets. Although further detailed studies are required, it seems reasonable to propose even at this early stage that ferroptosis may play a significant role in metal toxicity, and its modulation may be considered as a potential therapeutic tool for the amelioration of metal toxicity.

Indexed as

FerroptosisAntioxidantsIronLipid PeroxidationOxidative StressReactive Oxygen SpeciesAntioxidantsIronReactive Oxygen SpeciesArsenicCadmiumCopperFerroptosisManganeseSelenium, toxicityZinc

Identifiers

PMID35727353
OpenAlexW4283217049

What Socratic holds

Textmetadata
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 Socratic graph.