Evidence map›Paper›PMID 41184494›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2025

Exploring the potential relationship between serum biomarkers in obese individuals and cancer using FTIR, metabolomics, and lipidomics.

Maria Eduarda Marques, Natália Ferreira Silva, Fernanda Naves Araújo do Prado Mascarenhas, Tatiana Carla Tomiosso, Robson José de Oliveira Júnior, Ricardo Rodrigues, Hebreia Oliveira Almeida-Souza, Mário Machado Martins, Luciana Machado Bastos, Arlene Bispo Dos Santos Nossol and 6 more

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In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

16 authors.

Maria Eduarda Marques *Institute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0009-0005-8359-2199
Natália Ferreira Silva *Institute of Biomedical Science, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0001-6277-0367
Fernanda Naves Araújo do Prado MascarenhasInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-3799-5844
Tatiana Carla TomiossoInstitute of Biomedical Science, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0001-8518-1688
Robson José de Oliveira JúniorInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0001-8453-3194
Ricardo RodriguesMedicine Faculty, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-7093-3848
Hebreia Oliveira Almeida-SouzaInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0009-0007-6319-2598
Mário Machado MartinsInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0001-7381-2788
Luciana Machado BastosInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-6637-0149
Arlene Bispo Dos Santos NossolInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0001-6524-3343
Tiara da Costa SilvaInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-0370-8405
Camila Moreira de AndradeInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-4164-2283
Marco Fidel Guevara-VegaInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0003-2332-0886
Robinson Sabino-SilvaInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-2104-5780
Carlos Ueira-VieiraInstitute of Biotecnology, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil.ORCID http://orcid.org/0000-0002-8369-9069
Renata Graciele ZanonInstitute of Biomedical Science, Federal University of Uberlandia, UFU, Uberlândia, MG, Brazil. rezanon@ufu.br.ORCID http://orcid.org/0000-0001-5930-3821

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 403193/2022-2Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-01483-22Fundação de Amparo à Pesquisa do Estado de Minas Gerais CBB-APQ-03613-17
6 · The paper itself

Abstract

introductionRobust evidence endorsed by the International Agency for Research on Cancer demonstrates that excess body fat represents a risk for the development of at least 13 types of cancer.

objectiveWe investigated the serum of individuals with obesity who had no history of cancer (either personal or familial) to identify biomarkers.

methods45 individuals were included in this study; they did not show significant differences regarding age, sex, or physical activity. A quality-of-life questionnaire was administered to all participants, revealing that the obese group self-reported difficulties in functional capacity and a greater association with comorbidities, notably hypertension. FTIR, metabolomic, and lipidomic analyses were performed to identify spectral peaks, metabolic, and lipids differentiating between the NO (non-obese) and OB (obese) groups.

resultsThe identified peaks are predominantly associated with profiles of lipids, carbohydrates, and nitrogenous compounds. A total of six metabolites and lipids were identified at different levels in the serum of the OB group that have a direct relationship with the development or metabolism of cancer cells (three metabolites and three lipids). Among these, some suggest a reduced likelihood of cancer development, while others indicate an increased potential for cancer development. In this context, we can highlight two substances: the metabolite 4-Hydroxyphenylglyoxylate, which is reduced in the serum of individuals with obesity, and the lipid Glycidyl palmitate, which is elevated in individuals with obesity.

conclusion4-Hydroxyphenylglyoxylate and Glycidyl palmitate can be used as biomarkers for cancer and obesity correlation. New experiments manipulating these substances may contribute to a better understanding of their interactions with cancer cells.

Indexed as

BiomarkersBiomarkers, TumorLipidomicsMetabolomicsNeoplasmsObesityAdultAgedFemaleHumansLipidsMaleMiddle AgedSpectroscopy, Fourier Transform InfraredBiomarkersBiomarkers, TumorLipidsCancerMetabolomicsNeoplasiaObesityOverweight

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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.