Evidence map›Paper›PMID 40595283›Full record

ArticleBritish journal of cancer2025

Chemotherapy-induced neuropathy in monomethyl Auristatin E treatment: prevention by lithium.

Matheus F Itaborahy, Isadora Z L F Feng, Uri F Vieira-Machado, Izabela B da Silveira, Thalita M Valverde, Guilherme M J Costa, Jennifer D S Guimarães, Daniela Laet-Souza, Carlos Malamut, M Alessandra F Martins and 13 more

Abstract read
In one paragraph

Article in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

23 authors.

Matheus F Itaborahy *Departamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Isadora Z L F Feng *Departamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Uri F Vieira-Machado *Departamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Izabela B da SilveiraDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Thalita M ValverdeDepartmento de Morfologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Guilherme M J CostaDepartmento de Morfologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Jennifer D S GuimarãesDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Daniela Laet-SouzaDepartmento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Carlos MalamutCentro de Desenvolvimento de Tecnologia Nuclear (CDTN/CNEN), Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
M Alessandra F MartinsDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Júlia M MarquesDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Julia Rezende-RibeiroDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Vladimir GorshkovDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
Frank KjeldsenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
Maria Eduarda S FavalessaDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Izabella F AcipresteDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Thiago Verano-BragaDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Hernandes F CarvalhoDepartmento de Biologia Estrutural e Funcional, Universidade Estadual de Campinas, Campinas, SP, Brazil.ORCID http://orcid.org/0000-0002-3080-9447
André G OliveiraDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Marlon Lemos DiasCentro de Pesquisa de Medicina de Precisão, Instituto de Biofísica Carlos Chagas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-9354-7280
Alfredo M GoesDepartmento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Barbara E EhrlichDepartment of Pharmacology, Yale University School of Medicine, New Haven, CT, USA. barbara.ehrlich@yale.edu.
M Fatima LeiteDepartamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil. leitemd@ufmg.br.ORCID http://orcid.org/0000-0001-9709-8865

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing number of cancer survivors, thanks to improved cancer treatments, has escalated the prevalence of adverse effects, especially chemotherapy-induced peripheral neuropathy (CIPN) and chemotherapy-induced cognitive impairment (CICI). New drug classes, including antibody-drug conjugates (ADCs), are being developed to target cancer cells and avoid noxious effects. Despite the efforts, ADCs present a high prevalence of neuropathy. A drug often employed in approved ADCs is Monomethyl Auristatin E (MMAE), a microtubule-based agent. The aim of this study was to investigate the sensory and cognitive effects of MMAE in a mouse model and test the potential use of lithium to alleviate MMAE-induced neuropathy.

methodsWe developed a model of MMAE-induced CIPN and CICI and used behavior and sensory tests to analyze these conditions. We also evaluated calcium signaling and protein levels in neuropathic tissues and tumor progression upon treatments with lithium and MMAE.

resultsMMAE administration leads to loss of peripheral sensitivity and cognitive impairment and lithium prevents both central and peripheral neuropathies induced by chemotherapy, without affecting the antitumor activity of MMAE.

conclusionThis study shows that strategies including lithium pretreatment can prevent both central and peripheral neuropathies induced by chemotherapy to improve quality of life of cancer survivors.

Indexed as

Antineoplastic AgentsChemotherapy-Related Cognitive ImpairmentLithiumOligopeptidesPeripheral Nervous System DiseasesAnimalsDisease Models, AnimalFemaleHumansImmunoconjugatesMaleMiceAntineoplastic AgentsImmunoconjugatesLithiummonomethyl auristatin EOligopeptides

Identifiers

PMID40595283
PMCPMC12405523

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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.