Ferroptosis: The Greasy Side of Cell Death.

Abstract:

:Ferroptosis is a form of cell death that requires phospholipid peroxidation and has attracted increased attention, both as a means to eradicate tumors resistant to standard chemotherapy and for its potential contribution to tissue damage such as in ischemia/reperfusion. The center stage taken by phospholipid peroxidation in ferroptosis is highlighted by recent discoveries that demonstrate an intricate regulation of both the metabolism of polyunsaturated fatty acids as well as mechanisms leading to their oxidation. These metabolic steps converge at the point of ferroptosis execution through mechanisms that are now only starting to be understood. In this short review, we provide an appraisal of some of the recent advances in the understanding of the ferroptosis process and also provide some perspectives of where this knowledge could take us.

journal_name

Chem Res Toxicol

authors

Friedmann Angeli JP,Miyamoto S,Schulze A

doi

10.1021/acs.chemrestox.8b00349

subject

Has Abstract

pub_date

2019-03-18 00:00:00

pages

362-369

issue

3

eissn

0893-228X

issn

1520-5010

journal_volume

32

pub_type

杂志文章,评审
  • Reaction of CO2 with ONOO-: One Molecule of CO2 Is Not Enough.

    abstract::With CO2 present in excess, ONOO- reacts to form an adduct in solution and in the solid state, most likely ONOOCO2-. In solution, the adduct appears within 2 ms and absorbs at 300 with an extinction coefficient, which is either 50% or 100% (preferred) of that of ONOO-, 1.70 × 103 M-1 cm-1, and at 685 nm with an extinc...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.8b00068

    authors: Serrano-Luginbuehl S,Kissner R,Koppenol WH

    更新日期:2018-08-20 00:00:00

  • Intracellular activation of cytotoxic agents: kinetic models for methylnitrosoureas and N-methyl-N'-nitro-N-nitrosoguanidine in cell culture.

    abstract::The cytotoxic activity of N-methyl-N-nitrosourea (MNU), streptozotocin, and N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) was determined in cell culture by using a P388 cell growth rate inhibition assay. These agents appear to have very different activities when inhibition is related to the agent concentration in the cu...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00009a006

    authors: Weinkam RJ,Dolan ME

    更新日期:1989-05-01 00:00:00

  • Oncometabolites d- and l-2-Hydroxyglutarate Inhibit the AlkB Family DNA Repair Enzymes under Physiological Conditions.

    abstract::Cancer-associated mutations often lead to perturbed cellular energy metabolism and accumulation of potentially harmful oncometabolites. One example is the chiral molecule 2-hydroxyglutarate (2HG); its two stereoisomers (d- and l-2HG) have been found at abnormally high concentrations in tumors featuring anomalous metab...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.7b00009

    authors: Chen F,Bian K,Tang Q,Fedeles BI,Singh V,Humulock ZT,Essigmann JM,Li D

    更新日期:2017-04-17 00:00:00

  • Molecular recognition between oligopeptides and nucleic acids: DNA binding specificity of a series of bis netropsin analogues deduced from footprinting analysis.

    abstract::A series of tether-linked bis netropsins have been synthesized in order to assess the phasing problem, which arises because of the lack of dimensional correspondence between oligopeptides and oligonucleotides in DNA binding characteristics. The consequences of incorporating variable-length flexible and rigid tethers [...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00014a013

    authors: Kissinger KL,Dabrowiak JC,Lown JW

    更新日期:1990-03-01 00:00:00

  • Arsenic-induced carcinogenesis--oxidative stress as a possible mode of action and future research needs for more biologically based risk assessment.

    abstract::Exposure to inorganic arsenic (iAs) induces cancer in human lungs, urinary bladder, skin, kidney, and liver, with the majority of deaths from lung and bladder cancer. To date, cancer risk assessments for iAs have not relied on mechanistic data, as we have lacked sufficient understanding of arsenic's pharmacokinetics a...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx900343d

    authors: Kitchin KT,Conolly R

    更新日期:2010-02-15 00:00:00

  • Large-scale synthesis of the catechol metabolites of diethylstilbestrol and hexestrol.

    abstract::Diethylstilbestrol (DES) and hexestrol (HES) are carcinogenic synthetic estrogens. The major metabolites of these compounds are their catechol derivatives, 3'-OH-DES and 3'-OH-HES. Oxidation of these metabolites leads to the electrophilic quinones, which are presumably involved in the tumor-initiating process. A synth...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx970140v

    authors: Jan ST,Rogan EG,Cavalieri EL

    更新日期:1998-05-01 00:00:00

  • Leveraging the Value of CDISC SEND Data Sets for Cross-Study Analysis: Incidence of Microscopic Findings in Control Animals.

    abstract::Implementation of the Clinical Data Interchange Standards Consortium (CDISC)'s Standard for Exchange of Nonclinical Data (SEND) by the United States Food and Drug Administration Center for Drug Evaluation and Research (US FDA CDER) has created large quantities of SEND data sets and a tremendous opportunity to apply la...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.0c00317

    authors: Carfagna MA,Anderson J,Eley C,Fukushima T,Horvath J,Houser W,Larsen B,Page T,Russo D,Sloan C,Snyder K,Thompson R,Ullmann G,Whittaker M

    更新日期:2020-12-16 00:00:00

  • Genotoxicity-related chemistry of human metabolites of benzo[ghi]perylene (B[ghi]P) investigated using electro-optical arrays and DNA/microsome biocolloid reactors with LC-MS/MS.

    abstract::There is limited and sometimes contradictory information about the genotoxicity of the polycyclic aromatic hydrocarbon benzo[ghi]perylene (B[ghi]P). Using recently developed metabolic toxicity screening arrays and a biocolloid reactor-LC-MS/MS approach, both featuring films of DNA and human metabolic enzymes, we demon...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx400147c

    authors: Pan S,Li D,Zhao L,Schenkman JB,Rusling JF

    更新日期:2013-08-19 00:00:00

  • Adenine adducts with diepoxybutane: isolation and analysis in exposed calf thymus DNA.

    abstract::1,3-Butadiene (BD) is a high-volume industrial chemical and a common environmental pollutant. Although BD is classified as a "probable human carcinogen", only limited evidence is available for its tumorigenic effects in occupationally exposed populations. Animal studies show a surprisingly high sensitivity of mice to ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx9700681

    authors: Tretyakova N,Sangaiah R,Yen TY,Gold A,Swenberg JA

    更新日期:1997-10-01 00:00:00

  • Aortic Binding of AZD5248: Mechanistic Insight and Reactivity Assays To Support Lead Optimzation.

    abstract::The oral dipeptidyl peptidase 1 (DPP1) inhibitor AZD5248 showed aortic binding in a rat quantitative whole-body autoradiography (QWBA) study, and its development was terminated prior to human dosing. A mechanistic hypothesis for this finding was established invoking reactivity with aldehydes involved in the cross-link...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.5b00236

    authors: Bragg RA,Brocklehurst S,Gustafsson F,Goodman J,Hickling K,MacFaul PA,Swallow S,Tugwood J

    更新日期:2015-10-19 00:00:00

  • Allergic contact dermatitis--formation, structural requirements, and reactivity of skin sensitizers.

    abstract::Contact allergy is caused by a wide range of chemicals after skin contact. Its clinical manifestation, allergic contact dermatitis (ACD), is developed upon repeated contact with the allergen. This perspective focuses on two areas that have yielded new useful information during the last 20 years: (i) structure-activity...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx7002239

    authors: Karlberg AT,Bergström MA,Börje A,Luthman K,Nilsson JL

    更新日期:2008-01-01 00:00:00

  • N-Glycosylation of pig flavin-containing monooxygenase form 1: determination of the site of protein modification by mass spectrometry.

    abstract::By using a combination of biochemical methods (i.e., endoglycosidase H digestion and immunoblot and plant lectin binding studies), it was verified that pig flavin-containing monooxygenase (FMO1) was N-glycosylated. By using mass spectrometry approaches [i.e., peptide mapping, gas chromatography/mass spectrometry, micr...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx980117p

    authors: Korsmeyer KK,Guan S,Yang ZC,Falick AM,Ziegler DM,Cashman JR

    更新日期:1998-10-01 00:00:00

  • Ring addition of the alpha-amino group of glutathione increases the reactivity of benzoquinone thioethers.

    abstract::2-(Glutathion-S-yl)-1,4-benzoquinone was found to be remarkably unstable in phosphate buffer (pH 7.4) even in the absence of oxygen. Intramolecular addition of the alpha-amino group of the glutamate residue to the quinone ring yielded ultimately 2,3-(glutathion-N, S-yl)-1,4-benzoquinone and 2,6-(glutathion-N,S-yl)-1,4...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx9800699

    authors: Alt C,Eyer P

    更新日期:1998-10-01 00:00:00

  • Drug metabolite-specific lymphocyte responses in sulfamethoxazole allergic patients with cystic fibrosis.

    abstract::Sulfamethoxazole (SMX) is an important antibiotic in the management of patients with cystic fibrosis, but allergic reactions may develop thus restricting therapy. The aim of this study was to utilize drug (metabolite) antigens to diagnose SMX-mediated allergic reactions in patients with cystic fibrosis. Lymphocytes fr...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx100151v

    authors: Lavergne SN,Whitaker P,Peckham D,Conway S,Park BK,Naisbitt DJ

    更新日期:2010-06-21 00:00:00

  • Measurement of oxidative DNA damage by catechol estrogens and analogues in vitro.

    abstract::The growth-promoting effects of estrogens in hormone-dependent tumor tissues involve receptor-mediated pathways that are well-recognized; however, the role of estrogens in tumor initiation remains controversial. Estrogen metabolites, primarily the catechol estrogens (CE's), have been implicated in tumor initiation via...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx980128i

    authors: Mobley JA,Bhat AS,Brueggemeier RW

    更新日期:1999-03-01 00:00:00

  • Detection and identification of metabolites of microcystins formed in vivo in mouse and rat livers.

    abstract::The hepatic metabolism of microcystins (MCs), potent cyclic peptide hepatotoxins produced by cyanobacteria, was studied by i.p. injection in mice and rats. An immunoaffinity purification method using an anti-MC-LR monoclonal antibody showed a remarkable effect on the removal of contaminants in the hepatic cytosol and ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx960085a

    authors: Kondo F,Matsumoto H,Yamada S,Ishikawa N,Ito E,Nagata S,Ueno Y,Suzuki M,Harada K

    更新日期:1996-12-01 00:00:00

  • Trans Lipid Library: Synthesis of Docosahexaenoic Acid (DHA) Monotrans Isomers and Regioisomer Identification in DHA-Containing Supplements.

    abstract::Docosahexaenoic acid (DHA) is a semiessential polyunsaturated fatty acid (PUFA) for eukaryotic cells that is found in natural sources such as fish and algal oils and widely used as an ingredient for omega-3 containing foods or supplements. DHA effects are connected to its natural structure with six cis double bonds, b...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.8b00021

    authors: Menounou G,Giacometti G,Scanferlato R,Dambruoso P,Sansone A,Tueros I,Amézaga J,Chatgilialoglu C,Ferreri C

    更新日期:2018-03-19 00:00:00

  • Surface modification of quartz inhibits toxicity, particle uptake, and oxidative DNA damage in human lung epithelial cells.

    abstract::Quartz (crystalline silica) is not consistently carcinogenic across different industries where similar quartz exposure occurs. In addition, there are reports that surface modification of quartz affects its cytotoxicity, inflammogenicity, and fibrogenicity. Taken together, these data suggest that the carcinogenicity of...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx025558u

    authors: Schins RP,Duffin R,Höhr D,Knaapen AM,Shi T,Weishaupt C,Stone V,Donaldson K,Borm PJ

    更新日期:2002-09-01 00:00:00

  • Use of Zebrafish in Drug Discovery Toxicology.

    abstract::Unpredicted human safety events in clinical trials for new drugs are costly in terms of human health and money. The drug discovery industry attempts to minimize those events with diligent preclinical safety testing. Current standard practices are good at preventing toxic compounds from being tested in the clinic; howe...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/acs.chemrestox.9b00335

    authors: Cassar S,Adatto I,Freeman JL,Gamse JT,Iturria I,Lawrence C,Muriana A,Peterson RT,Van Cruchten S,Zon LI

    更新日期:2020-01-21 00:00:00

  • Chemical Interaction of Protein Cysteine Residues with Reactive Metabolites of Methyleugenol.

    abstract::Methyleugenol (ME), an alkenylbenzene compound, is a natural ingredient of several herbs and is used as flavoring agent in foodstuffs and fragrance in cosmetics. The hepatotoxicity, cytotoxicity, and carcinogenesis of ME have been well documented, and metabolic activation has been suggested to involve in ME-induced to...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.6b00290

    authors: Feng Y,Wang H,Wang Q,Huang W,Peng Y,Zheng J

    更新日期:2017-02-20 00:00:00

  • Identification of tamoxifen-DNA adducts formed by alpha-sulfate tamoxifen and alpha-acetoxytamoxifen.

    abstract::alpha-Sulfate trans-tamoxifen and alpha-sulfate cis-tamoxifen were synthesized as proposed active metabolites of tamoxifen that react with DNA. alpha-Acetoxytamoxifen was prepared as a model-activated form to produce a reactive carbocation. Calf thymus DNA was reacted with alpha-hydroxytamoxifen or the activated forms...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx960114h

    authors: Dasaradhi L,Shibutani S

    更新日期:1997-02-01 00:00:00

  • Preclinical strategy to reduce clinical hepatotoxicity using in vitro bioactivation data for >200 compounds.

    abstract::Drug-induced liver injury is the most common cause of market withdrawal of pharmaceuticals, and thus, there is considerable need for better prediction models for DILI early in drug discovery. We present a study involving 223 marketed drugs (51% associated with clinical hepatotoxicity; 49% non-hepatotoxic) to assess th...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300075j

    authors: Sakatis MZ,Reese MJ,Harrell AW,Taylor MA,Baines IA,Chen L,Bloomer JC,Yang EY,Ellens HM,Ambroso JL,Lovatt CA,Ayrton AD,Clarke SE

    更新日期:2012-10-15 00:00:00

  • Endocrine disruption screening by protein and gene expression of vitellogenin in freshly isolated and cryopreserved rainbow trout hepatocytes.

    abstract::Xenobiotics may activate the estrogen receptor, resulting in alteration of normal endocrine functions in animals and humans. Consequently, this necessitates development of assay end points capable of identifying estrogenic xenobiotics. In the present study, we screened the potential estrogenicity of chemicals via thei...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx5002089

    authors: Markell LK,Mingoia RT,Peterson HM,Yao J,Waters SM,Finn JP,Nabb DL,Han X

    更新日期:2014-08-18 00:00:00

  • Identification and characterization of deoxyguanosine adducts of methyl vinyl ketone and ethyl vinyl ketone. Genotoxicity of the ketones in the SOS Chromotest.

    abstract::The reaction of the alpha, beta-unsaturated ketones methyl vinyl ketone (MVK) and ethyl vinyl ketone (EVK) with nucleosides and 5'-mononucleotides was studied. The genotoxic activity of MVK and EVK in the SOS Chromotest was investigated. Three different types of adducts with deoxyguanosine were found and their structu...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00019a007

    authors: Eder E,Hoffman C,Deininger C

    更新日期:1991-01-01 00:00:00

  • Highly galloylated tannin fractions from witch hazel (Hamamelis virginiana) bark: electron transfer capacity, in vitro antioxidant activity, and effects on skin-related cells.

    abstract::Witch hazel ( Hammamelis virginiana) bark is a rich source of both condensed and hydrolizable oligomeric tannins. From a polyphenolic extract soluble in both ethyl acetate and water, we have generated fractions rich in pyrogallol-containing polyphenols (proanthocyanidins, gallotannins, and gallates). The mixtures were...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700425n

    authors: Touriño S,Lizárraga D,Carreras A,Lorenzo S,Ugartondo V,Mitjans M,Vinardell MP,Juliá L,Cascante M,Torres JL

    更新日期:2008-03-01 00:00:00

  • Investigations on the effect of O(6)-benzylguanine on the formation of dG-dC interstrand cross-links induced by chloroethylnitrosoureas in human glioma cells using stable isotope dilution high-performance liquid chromatography electrospray ionization tand

    abstract::Chloroethylnitrosoureas (CENUs) are bifunctional alkylating agents widely used for the clinical treatment of cancer. They exert anticancer activity by inducing DNA interstrand cross-links (ICLs) within GC base pairs to form dG-dC cross-links. This lesion inhibits DNA double strand separation during replication and tra...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500143b

    authors: Sun G,Zhao L,Fan T,Li S,Zhong R

    更新日期:2014-07-21 00:00:00

  • Protein modification by acrolein: formation and stability of cysteine adducts.

    abstract::The toxicity of the ubiquitous pollutant and endogenous metabolite, acrolein, is due in part to covalent protein modifications. Acrolein reacts readily with protein nucleophiles via Michael addition and Schiff base formation. Potential acrolein targets in protein include the nucleophilic side chains of cysteine, histi...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx800465m

    authors: Cai J,Bhatnagar A,Pierce WM Jr

    更新日期:2009-04-01 00:00:00

  • 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol) inhibits peroxynitrite-mediated phenol nitration.

    abstract::Peroxynitrite (PN), a very reactive oxidant formed by the combination of superoxide and nitric oxide, appears to play a role in producing tissue damage in a number of inflammatory conditions. Pharmacological scavenging and decomposition of PN within these areas has therapeutic value in several tissue injury models. Re...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx990159t

    authors: Carroll RT,Galatsis P,Borosky S,Kopec KK,Kumar V,Althaus JS,Hall ED

    更新日期:2000-04-01 00:00:00

  • Atrazine Triggers the Extrinsic Apoptosis Pathway in Lymphocytes of the Frog Pelophylax nigromaculata in Vivo.

    abstract::Atrazine (ATR) is extensively used worldwide as an herbicide, with a global ecological influence. The widespread distribution of herbicides may be one of the possible reasons for the decline in the global amphibian population. The acute toxicity and potential toxicological mechanisms of ATR on the immune system of fro...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.5b00238

    authors: Jia X,Wang D,Gao N,Cao H,Zhang H

    更新日期:2015-10-19 00:00:00

  • Synthesis and characterization of bay region halohydrins derived from Benzo[a]pyrene diol epoxide and their role as intermediates in halide-catalyzed cis adduct formation.

    abstract::The bay region epoxide of benzo[a]pyrene (anti-BPDE) alkylates DNA to form adducts with >98% trans stereochemistry. Halide ions catalyze this reaction; however, this pathway is characterized by the formation of adducts with altered cis stereochemistry. Bay region halohydrins are possible intermediates in these reactio...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx980056v

    authors: Song Q,Negrete GR,Wolfe AR,Wang K,Meehan T

    更新日期:1998-09-01 00:00:00