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Uncovering Metabolic Alterations in HCT-116 Colon Cancer Cells upon Exposure to Bamboo Leaf Extract Obtained from Guadua incana Londoño

dc.contributor.authorChitiva, Luis Carlos [UNESP]
dc.contributor.authorSantamaría-Torres, Mary Andrea
dc.contributor.authorRezende-Teixeira, Paula
dc.contributor.authorBorlot, Jessica Rodrigues Pereira de Oliveira
dc.contributor.authorRomagna, Rodrigo de Almeida
dc.contributor.authorLondoño, Ximena
dc.contributor.authorKitagawa, Rodrigo Rezende
dc.contributor.authorCosta-Lotufo, Leticia V.
dc.contributor.authorPrieto-Rodríguez, Juliet A.
dc.contributor.authorCastro-Gamboa, Ian [UNESP]
dc.contributor.authorCosta, Geison Modesti
dc.contributor.institutionPontificia Universidad Javeriana
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidad de los Andes
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionFederal University of Espírito Santo (UFES)
dc.contributor.institutionUniversidad Nacional de Colombia
dc.date.accessioned2025-04-29T18:38:05Z
dc.date.issued2024-07-01
dc.description.abstractMetabolic alterations are increasingly recognized as important aspects of colorectal cancer (CRC), offering potential avenues for identifying therapeutic targets. Previous studies have demonstrated the cytotoxic potential of bamboo leaf extract obtained from Guadua incana (BLEGI) against HCT-116 colon cancer cells. However, the altered metabolic pathways in these tumor cells remain unknown. Therefore, this study aimed to employ an untargeted metabolomic approach to reveal the metabolic alterations of the endometabolome and exometabolome of HCT-116 cells upon exposure to BLEGI treatment. First, a chemical characterization of the BLEGI was conducted through liquid chromatography coupled with mass spectrometry (LC-MS). Next, we assessed cell viability via MTT and morphological analysis using an immunofluorescence assay against colon cancer cells, and anti-inflammatory activity using an LPS-stimulated macrophage model. Subsequently, we employed LC-MS and proton nuclear magnetic resonance (1H-NMR) to investigate intra- and extracellular changes. Chemical characterization primarily revealed the presence of compounds with a flavone glycoside scaffold. Immunofluorescence analysis showed condensed chromatin and subsequent formation of apoptotic bodies, suggesting cell death by apoptosis. The results of the metabolomic analysis showed 98 differential metabolites, involved in glutathione, tricarboxylic acid cycle, and lipoic acid metabolism, among others. Additionally, BLEGI demonstrated significant nitric oxide (NO) inhibitory capacity in macrophage cells. This study enhances our understanding of BLEGI’s possible mechanism of action and provides fresh insights into therapeutic targets for treating this disease.en
dc.description.affiliationGrupo de Investigación Fitoquímica Universidad Javeriana (GIFUJ) Department of Chemistry Faculty of Sciences Pontificia Universidad Javeriana
dc.description.affiliationNúcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais (NuBBE) Institute of Chemistry São Paulo State University (UNESP)
dc.description.affiliationUniversidad de los Andes
dc.description.affiliationLaboratório de Farmacologia de Produtos Naturais Marinhos Institute of Biomedical Sciences University of São Paulo
dc.description.affiliationLaboratório de Triagem Biológica de Produtos Naturais Department of Pharmaceutical Sciences Federal University of Espírito Santo (UFES)
dc.description.affiliationFaculty of Agricultural Sciences Universidad Nacional de Colombia
dc.description.affiliationUnespNúcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais (NuBBE) Institute of Chemistry São Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.3390/molecules29132985
dc.identifier.citationMolecules, v. 29, n. 13, 2024.
dc.identifier.doi10.3390/molecules29132985
dc.identifier.issn1420-3049
dc.identifier.scopus2-s2.0-85198487016
dc.identifier.urihttps://hdl.handle.net/11449/298750
dc.language.isoeng
dc.relation.ispartofMolecules
dc.sourceScopus
dc.subjectanti-inflammatory activity
dc.subjectbamboo leaf extract
dc.subjectcytotoxic activity
dc.subjectendometabolome
dc.subjectexometabolome
dc.subjectGuadua incana
dc.subjectHCT-116 cells
dc.subjectmetabolomics
dc.titleUncovering Metabolic Alterations in HCT-116 Colon Cancer Cells upon Exposure to Bamboo Leaf Extract Obtained from Guadua incana Londoñoen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0003-1422-5545[1]
unesp.author.orcid0009-0004-9294-7871[5]
unesp.author.orcid0000-0002-1577-1356[6]
unesp.author.orcid0000-0003-1861-5153[8]
unesp.author.orcid0000-0002-7064-2389[9]
unesp.author.orcid0000-0002-2353-0181[10]
unesp.author.orcid0000-0003-2449-1986[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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