Evidence map›Paper›PMID 41654145›Full record

ArticleFree radical biology & medicine2026

What lies beyond thioredoxin reductase? Cyclometallated gold compounds reveal Sec selectivity in glutathione peroxidases.

Ioannis Kanavos, Douglas H Nakahata, Madeleine S Barrett, Ancély F Dos Santos, Maria Zubiria-Ulacia, German E Pieslinger, Ana Beatriz da Silva Teixeira, Isadora Medeiros, Clarissa Ribeiro Reily Rocha, Jonas Eberle and 7 more

Abstract read
In one paragraph

Article in Free radical biology & medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Ioannis KanavosUniversité de Pau et des Pays de l'Adour, E2S UPPA, CNRS, IPREM UMR 5254, 2 Av. du Presidnet Pierre Angotcedex 09, 64053, Pau, France.
Douglas H NakahataDonostia International Physics Center - DIPC, Paseo de Manuel Lardizabal 4, Euskadi, 20018, Donostia, Gipuzkoa, Spain.
Madeleine S BarrettDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE, 171 77, Stockholm, Sweden; Early Translation Branch, National Center for Advancing Translational Sciences, National Institute of Health, 9800 Medical Center Drive, Rockville, MD, 20850, United States.
Ancély F Dos SantosRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany.
Maria Zubiria-UlaciaDonostia International Physics Center - DIPC, Paseo de Manuel Lardizabal 4, Euskadi, 20018, Donostia, Gipuzkoa, Spain; Polimero eta Material Aurreratuak: Fisika, Kimika eta Teknologia, Kimika Fakultatea, Euskal Herriko Unibertsitatea UPV/EHU, Paseo Manuel de Lardizabal 3, Euskadi, 20018, Donostia, Gipuzkoa, Spain.
German E PieslingerDonostia International Physics Center - DIPC, Paseo de Manuel Lardizabal 4, Euskadi, 20018, Donostia, Gipuzkoa, Spain; CONICET-Universidad de Buenos Aires, Instituto de Química y Fisicoquímica Biológicas (IQUIFIB), Buenos Aires, C1113AAD, Argentina.
Ana Beatriz da Silva TeixeiraRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany; Universidade Federal de São Paulo (UNIFESP), Departamento de Oncologia Clínica e Experimental, São Paulo, 04037-003, Brazil.
Isadora MedeirosRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany; Departamento de Bioquímica, Instituto de Química (IQUSP), Universidade de São Paulo, São Paulo, 05508-000, Brazil.
Clarissa Ribeiro Reily RochaRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany; Universidade Federal de São Paulo (UNIFESP), Departamento de Oncologia Clínica e Experimental, São Paulo, 04037-003, Brazil.
Jonas EberleRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany.
Ryszard LobinskiUniversité de Pau et des Pays de l'Adour, E2S UPPA, CNRS, IPREM UMR 5254, 2 Av. du Presidnet Pierre Angotcedex 09, 64053, Pau, France; Chair of Analytical Chemistry, Warsaw University of Technology, 00-664, Warsaw, Poland.
Jon Mattin MatxainDonostia International Physics Center - DIPC, Paseo de Manuel Lardizabal 4, Euskadi, 20018, Donostia, Gipuzkoa, Spain; Polimero eta Material Aurreratuak: Fisika, Kimika eta Teknologia, Kimika Fakultatea, Euskal Herriko Unibertsitatea UPV/EHU, Paseo Manuel de Lardizabal 3, Euskadi, 20018, Donostia, Gipuzkoa, Spain.
Matthew D HallEarly Translation Branch, National Center for Advancing Translational Sciences, National Institute of Health, 9800 Medical Center Drive, Rockville, MD, 20850, United States.
José P Friedmann AngeliRudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Würzburg, Germany.
Elias S J ArnérDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE, 171 77, Stockholm, Sweden; Department of Selenoprotein Research and the National Tumor Biology Laboratory, National Institute of Oncology, 1122, Budapest, Hungary.
Luisa RongaUniversité de Pau et des Pays de l'Adour, E2S UPPA, CNRS, IPREM UMR 5254, 2 Av. du Presidnet Pierre Angotcedex 09, 64053, Pau, France. Electronic address: luisa.ronga@univ-pau.fr.
Raphael E F de PaivaDonostia International Physics Center - DIPC, Paseo de Manuel Lardizabal 4, Euskadi, 20018, Donostia, Gipuzkoa, Spain. Electronic address: raphael.depaiva@dipc.org.

Funding

Intramural NIH HHS Z99 TR999999
6 · The paper itself

Abstract

Cyclometallated gold(III) compounds were evaluated for their chemoselective capability to promote C-Se coupling reactions under biocompatible conditions. Competitive reactions with selenium and sulfur substrates highlighted the preference for selenium, and this selectivity was further confirmed in selenopeptide models mimicking the GPx active site. Given that thioredoxin reductase (TXNRD1) is a canonical target for gold compounds, we confirmed that our complexes also inhibit this enzyme, with the two six-membered metallacycles exhibiting a higher potency than auranofin. Expanding beyond TXNRD1, the compounds were further investigated as inhibitors of other selenoenzymes, specifically glutathione peroxidase isoenzymes (GPx1, GPx4). The metallacycles were potent inhibitors of GPx1, while in vitro GPx4 inhibition was overall less pronounced, with LC/MS studies identifying selenocysteine (Sec51) as the primary arylation site on GPx1. We demonstrated that this chemoselectivity could be translated to an intracellular setting. The selectivity towards Sec over Cys was further explored using A375 GPx4 WT and A375 GPx4 U46C mutant cell lines, where proliferation assays showed a greater effect in the GPx4 WT cells. By integrating structural and functional insights across selenoenzyme families, this study reveals glutathione peroxidases as pivotal molecular targets of cyclometallated gold(III) compounds and lays the groundwork for designing selective Sec-targeting metallodrugs, an approach with untapped potential in anticancer therapy.

Indexed as

Enzyme InhibitorsGlutathione PeroxidaseGold CompoundsSelenocysteineThioredoxin-Disulfide ReductaseAuranofinCatalytic DomainCell Line, TumorGlutathione Peroxidase GPX1HumansSeleniumAuranofinEnzyme InhibitorsGlutathione PeroxidaseGlutathione Peroxidase GPX1Gold CompoundsSeleniumSelenocysteineThioredoxin-Disulfide Reductase

Identifiers

PMID41654145
PMCPMC13078601

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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.