Evidence map›Paper›PMID 40834150›Full record

ArticleEinstein (Sao Paulo, Brazil)2025

Membrane transporter genes predict chemoradiotherapy response in patients with cervical cancer.

Natália Gregório Custódio, Fábio Ribeiro Queiroz, Angelo Borges de Melo Neto, Brenda Martins Cavalcante, Laurence Rodrigues do Amaral, Telma Maria Rossi de Figueiredo Franco, Matheus de Souza Gomes, Vasco Ariston de Carvalho Azevedo, Letícia da Conceição Braga, Paulo Guilherme de Oliveira Salles and 1 more

Abstract read
In one paragraph

Article in Einstein (Sao Paulo, Brazil), 2025. 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

11 authors.

Natália Gregório CustódioLaboratory of Cellular and Molecular Genetics, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0000-0001-7902-4264
Fábio Ribeiro QueirozTranslational Research Laboratory, Research and Teaching Center, Instituto Mário Penna, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0000-0003-0238-5787
Angelo Borges de Melo NetoBioinformatics and Molecular Analysis Laboratory, Universidade Federal de Uberlândia, Patos de Minas, MG, Brazil.ORCID http://orcid.org/0000-0003-0978-2355
Brenda Martins CavalcanteLaboratory of Experimental Pharmacology, Faculdade de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0009-0002-5327-7751
Laurence Rodrigues do AmaralBioinformatics and Molecular Analysis Laboratory, Universidade Federal de Uberlândia, Patos de Minas, MG, Brazil.ORCID http://orcid.org/0000-0003-4681-5451
Telma Maria Rossi de Figueiredo FrancoTranslational Research Laboratory, Research and Teaching Center, Instituto Mário Penna, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0009-0004-4114-9183
Matheus de Souza GomesBioinformatics and Molecular Analysis Laboratory, Universidade Federal de Uberlândia, Patos de Minas, MG, Brazil.ORCID http://orcid.org/0000-0001-7352-3089
Vasco Ariston de Carvalho AzevedoLaboratory of Cellular and Molecular Genetics, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0000-0002-4775-2280
Letícia da Conceição BragaTranslational Research Laboratory, Research and Teaching Center, Instituto Mário Penna, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0000-0002-6181-9410
Paulo Guilherme de Oliveira SallesTranslational Research Laboratory, Research and Teaching Center, Instituto Mário Penna, Belo Horizonte, MG, Brazil.ORCID http://orcid.org/0000-0001-8839-3491
Wander de Jesus JeremiasLaboratory of Experimental Pharmacology, Faculdade de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0001-8204-6712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to explore membrane transporter gene expression as a predictive biomarker of chemoradiotherapy response in cervical cancer. The differential expression of ATP1B3 and SLCO1B3 accurately classified patients as responders or non-responders with 90% accuracy, highlighting their potential for personalized treatment strategies.

backgroundTwo gene groups with contrasting expression profiles were identified.

backgroundThe ATP1B3 and SLCOB3 gene profiles classified patients with 90% accuracy.

backgroundThe ATP1B3 and SLCOB3 gene signature is a potential predictor of treatment response.

introductionCervical cancer is the fourth most common cancer in women worldwide. Resistance to chemoradiotherapy in cervical cancer has been widely associated with membrane transport-related genes, particularly those encoding efflux transport proteins, such as the ATP-binding cassette family members (including P-glycoprotein), which act by expelling chemotherapeutic agents from tumor cells, as well as solute carrier proteins, whose expression impairs the uptake of antineoplastic drugs by cancer cells.

objectiveThis study aimed to identify specific membrane transport-related gene expression profiles as potential biomarkers for predicting chemoradiotherapy response in cervical cancer.

methodsCervical biopsies were collected from 31 patients (21 responders and 10 non-responders) at Hospital Luxemburgo - Instituto Mário Penna. Fluorescence-activated cell sorting was used to separate non-stem cancer cells from cervical cancer biopsies. cDNA libraries from the 21 responders and 10 non-responders were sequenced using the Illumina platform. Expression analysis was performed using R and the DESeq2 package, with differentially expressed genes identified based on log fold change >1 or <-1 and padj ≤0.05. WEKA software and decision tree methods were used to analyze membrane transporters.

resultsThe results revealed two major gene groups with contrasting differentially expressed genes profiles. The first group, comprising SLC35 and ATP13, was overexpressed in non-responders, while the second group, consisting of SLC25 and ATP6, was overexpressed in responders. Decision tree analysis revealed that ATP1B3 and SLCOB3 expression profiles accurately classified patients into responder and non-responder groups with 90% accuracy, indicating that ATP1B3 and SLCOB3 are potential predictors of chemoradiotherapy response.

conclusionOur results strongly suggest the presence of a candidate gene signature comprising ATP1B3 and SLCO1B3 that holds predictive value for chemoradiotherapy response in cervical cancer.

Indexed as

ATP Binding Cassette Transporter, Subfamily BChemoradiotherapyMembrane Transport ProteinsUterine Cervical NeoplasmsAdultAgedBiomarkers, TumorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMiddle AgedPredictive Value of TestsTreatment OutcomeATP Binding Cassette Transporter, Subfamily BBiomarkers, TumorMembrane Transport Proteins

Identifiers

PMID40834150
PMCPMC12539833

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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.