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GC-MS-based endometabolome analysis differentiates prostate cancer from normal prostate cells

dc.contributor.authorLima, Ana
dc.contributor.authorAraújo, Ana
dc.contributor.authorPinto, Joana
dc.contributor.authorJerónimo, Carmen
dc.contributor.authorHenrique, Rui
dc.contributor.authorBastos, Maria
dc.contributor.authorCarvalho, Márcia
dc.contributor.authorGuedes de Pinho, Paula
dc.date.accessioned2019-10-01T12:29:39Z
dc.date.available2019-10-01T12:29:39Z
dc.date.issued2018-03
dc.description.abstractProstate cancer (PCa) is an important health problem worldwide. Diagnosis and management of PCa is very complex because the detection of serum prostate specific antigen (PSA) has several drawbacks. Metabolomics brings promise for cancer biomarker discovery and for better understanding PCa biochemistry. In this study, a gas chromatography-mass spectrometry (GC-MS) based metabolomic profiling of PCa cell lines was performed. The cell lines include 22RV1 and LNCaP from PCa with androgen receptor (AR) expression, DU145 and PC3 (which lack AR expression), and one normal prostate cell line (PNT2). Regarding the metastatic potential, PC3 is from an adenocarcinoma grade IV with high metastatic potential, DU145 has a moderate metastatic potential, and LNCaP has a low metastatic potential. Using multivariate analysis, alterations in levels of several intracellular metabolites were detected, disclosing the capability of the endometabolome to discriminate all PCa cell lines from the normal prostate cell line. Discriminant metabolites included amino acids, fatty acids, steroids, and sugars. Six stood out for the separation of all the studied PCa cell lines from the normal prostate cell line: ethanolamine, lactic acid, β-Alanine, L-valine, L-leucine, and L-tyrosine.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.3390/metabo8010023pt_PT
dc.identifier.issn2218-1989
dc.identifier.issn2218-1989
dc.identifier.urihttp://hdl.handle.net/10284/8088
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationFEDER funds POCI/01/0145/FEDER/07728pt_PT
dc.relationNational funds (FCT/MEC, Fundação para a Ciência e a Tecnologia and Ministério da Educação e Ciência) under the Partnership Agreement PT2020 UID/MULTI/04378/2013pt_PT
dc.relationUFP Energy, Environment and Health Research Unit
dc.relation.publisherversionhttps://www.mdpi.com/2218-1989/8/1/23pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectProstate cancerpt_PT
dc.subjectCancer metabolomicspt_PT
dc.subjectCell linespt_PT
dc.subjectMetabolomicspt_PT
dc.subjectEndometabolomept_PT
dc.subjectGC-MSpt_PT
dc.titleGC-MS-based endometabolome analysis differentiates prostate cancer from normal prostate cellspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleUFP Energy, Environment and Health Research Unit
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FMulti%2F04546%2F2013/PT
oaire.citation.issue1pt_PT
oaire.citation.startPage23pt_PT
oaire.citation.titleMetabolitespt_PT
oaire.citation.volume8pt_PT
oaire.fundingStream6817 - DCRRNI ID
person.familyNameCarvalho
person.givenNameMarcia
person.identifier2017111
person.identifier.ciencia-id8B10-171E-E63E
person.identifier.orcid0000-0001-9884-4751
person.identifier.ridD-5999-2013
person.identifier.scopus-author-id7201413997
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication3837b828-ba57-47f7-a811-cce65e4922c6
relation.isAuthorOfPublication.latestForDiscovery3837b828-ba57-47f7-a811-cce65e4922c6
relation.isProjectOfPublicationcec3999e-2653-4788-916f-d2b5061d5728
relation.isProjectOfPublication.latestForDiscoverycec3999e-2653-4788-916f-d2b5061d5728

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