Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/26044
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dc.contributor.authorDERVEAUX, Elien-
dc.contributor.authorLOUIS, Evelyne-
dc.contributor.authorVANHOVE, Karolien-
dc.contributor.authorBERVOETS, Liene-
dc.contributor.authorMESOTTEN, Liesbet-
dc.contributor.authorTHOMEER, Michiel-
dc.contributor.authorADRIAENSENS, Peter-
dc.date.accessioned2018-06-18T08:27:43Z-
dc.date.available2018-06-18T08:27:43Z-
dc.date.issued2018-
dc.identifier.citationCosta Torres, Alba Fabiola (ed.). Lung Cancer: Latest Strategies for Diagnosis and Treatment, IntechOpen, p. 79-94-
dc.identifier.isbn9781789843491-
dc.identifier.urihttp://hdl.handle.net/1942/26044-
dc.description.abstractThe reprogrammed metabolism of cancer cells reflects itself in an alteration of metabolite concentrations, which in turn can be used to define a specific metabolic phenotype or fingerprint for cancer. In this contribution, a metabolism-based discrimination between lung cancer patients and healthy controls, derived from an analysis of human blood plasma by proton nuclear magnetic resonance (1H-NMR) spectroscopy, is described. This technique is becoming widely used in the field of metabolomics because of its ability to provide a highly informative spectrum, representing the relative metabolite concentrations. Cancer types are characterized by decreased or increased levels of specific plasma metabolites, such as glucose or lactate, compared to controls. Data analysis by multivariate statistics provides a classification model with high levels of sensitivity and specificity. Nuclear magnetic resonance (NMR) metabolomics might not only contribute to the diagnosis of lung cancer but also shows potential for treatment follow-up as well as for paving the way to a better understanding of disease-related diverting biochemical pathways.-
dc.description.sponsorshipThis study is part of the Limburg Clinical Research Program (LCRP) UHasselt-ZOL-Jessa and supported by Kom op tegen Kanker (Stand up to Cancer), the Flemish Cancer Society. The authors like to thank Prof. Dr. Eric de Jonge and Prof. Dr. Philip Caenepeel for their support in sample recruitment.-
dc.language.isoen-
dc.publisherIntechOpen-
dc.rights© 2018 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.subject.otherMetabolomics; human blood plasma; metabolic phenotype; 1H-NMR spectroscopy; metabolite spiking; multivariate OPLS-DA statistics; lung cancer; cancer cell metabolism; biomarker-
dc.titleDiagnosis of lung cancer: what metabolomics can contribute-
dc.typeBook Section-
dc.relation.edition1-
local.bibliographicCitation.authorsCosta Torres, Alba Fabiola-
dc.identifier.epage94-
dc.identifier.spage79-
local.bibliographicCitation.jcatB2-
local.publisher.placeLondon-
local.type.refereedRefereed-
local.type.specifiedBook Section-
dc.identifier.doi10.5772/intechopen.79258-
local.bibliographicCitation.btitleLung Cancer: Latest Strategies for Diagnosis and Treatment-
item.validationvabb 2020-
item.contributorDERVEAUX, Elien-
item.contributorLOUIS, Evelyne-
item.contributorVANHOVE, Karolien-
item.contributorBERVOETS, Liene-
item.contributorMESOTTEN, Liesbet-
item.contributorTHOMEER, Michiel-
item.contributorADRIAENSENS, Peter-
item.accessRightsOpen Access-
item.fullcitationDERVEAUX, Elien; LOUIS, Evelyne; VANHOVE, Karolien; BERVOETS, Liene; MESOTTEN, Liesbet; THOMEER, Michiel & ADRIAENSENS, Peter (2018) Diagnosis of lung cancer: what metabolomics can contribute. In: Costa Torres, Alba Fabiola (ed.). Lung Cancer: Latest Strategies for Diagnosis and Treatment, IntechOpen, p. 79-94.-
item.fulltextWith Fulltext-
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