Evidence map›Paper›PMID 41748761›Full record

ArticleArchives of toxicology2026

PEGylated liposomal fluopsin C triggers cuproptosis and ferroptosis pathways and suppresses 3D tumor spheroid growth in NCI-H460 cells.

Luan Vitor Alves de Lima, Matheus Felipe da Silva, Liana Martins de Oliveira, Maria Claudia Terkelli de Assis, Isabella Cristina Oliveira Carvalho, Isaura Maria Fuzinatto, Simone Cristine Semprebon, Renan Vinícius de Oliveira Nocetti, Danielle Lazarin-Bidoia, Celso Vataru Nakamura and 7 more

Abstract read
In one paragraph

Article in Archives of toxicology, 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.

Luan Vitor Alves de LimaLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil. luan.vitorlima@uel.br.ORCID 0000-0002-0360-2889
Matheus Felipe da SilvaLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Liana Martins de OliveiraLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Maria Claudia Terkelli de AssisLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Isabella Cristina Oliveira CarvalhoLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Isaura Maria FuzinattoLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Simone Cristine SemprebonLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Renan Vinícius de Oliveira NocettiLaboratory of Technological Innovation in Drug and Cosmetic Development, Department of Basic Health Sciences, Maringá State University, Maringá, Paraná, Brazil.
Danielle Lazarin-BidoiaLaboratory of Technological Innovation in Drug and Cosmetic Development, Department of Basic Health Sciences, Maringá State University, Maringá, Paraná, Brazil.
Celso Vataru NakamuraLaboratory of Technological Innovation in Drug and Cosmetic Development, Department of Basic Health Sciences, Maringá State University, Maringá, Paraná, Brazil.
Ingrid FelicidadeLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Sandra Regina LepriLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Phelipe Oliveira FavaronLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Mickely Liuti DealisLaboratory of Microbial Ecology, Department of Microbiology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Luis Fernando CabeçaChemistry Laboratory, Federal Technological University of Paraná, Londrina, Paraná, Brazil.
Galdino Andrade FilhoLaboratory of Microbial Ecology, Department of Microbiology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Mário Sérgio MantovaniLaboratory of Toxicological Genetics, Department of General Biology, Center for Biological Sciences, State University of Londrina, Londrina, Paraná, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copper-based metallodrugs are promising anticancer agents, but their toxicity limits clinical translation. This study evaluated the toxicological and molecular effects of PEGylated Fluopsin C (PEG-FlpC) in in vitro human non-small-cell lung carcinoma (NCI-H460) cells cultured as 2D monolayer and 3D spheroids. Cells were exposed to PEG-FlpC at its IC50 (1.0 µM) for 24 h. Flow cytometry revealed G₁-phase arrest and non-apoptotic cell death. PEG-FlpC markedly suppressed spheroid growth, with 2 × IC50-treated spheroids growing only 58.1% compared to 131.6% in the control. Ultrastructural analyses showed mitochondrial clustering and swelling, ER dilation, and cytoplasmic vacuolization. Gene profiling demonstrated downregulation of TP53 and BECN1, with upregulation of TP73 and SQSTM1, consistent with autophagy blockade and stress activation. PEG-FlpC modulated ferroptosis-related (GPX4, SLC7A11, and TFRC) and cuproptosis-related (ATP7B, MTF1, DLAT, and CDKN2A) genes. Pharmacological inhibition confirmed a predominantly copper-mediated mechanism, as TTM (10 µM) restored 77.7% of metabolic activity. Combined inhibition with TTM and Fer-1 (1 µM) further increased viability to 89.4%, indicating that PEG-FlpC induces non-apoptotic regulated cell death through an interconnected cuproptosis–ferroptosis mechanism associated with mitochondrial dysfunction.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungCuproptosisFerroptosisLung NeoplasmsSpheroids, CellularAmino Acid Transport System y+Beclin-1Cell Line, TumorHumansLiposomesPolyethylene GlycolsSequestosome-1 ProteinTumor Protein p73Tumor Suppressor Protein p53Amino Acid Transport System y+Antineoplastic AgentsBeclin-1BECN1 protein, humanLiposomesPolyethylene GlycolsSequestosome-1 ProteinSLC7A11 protein, humanSQSTM1 protein, humanTP53 protein, humanTP73 protein, humanTumor Protein p73Tumor Suppressor Protein p53MetallodrugNatural productsNon-apoptotic cell deathRegulated cell deathTargeted drug delivery

Identifiers

PMID41748761
PMCPMC13086880

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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.