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Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors

Purpose. The incidence of liver neoplasms is rising in USA. The purpose of this study was to determine metabolic profiles of liver tissue during early cancer development. Methods. We used the rabbit VX2 model of liver tumors (LT) and a control group consisting of sham animals implanted with Gelfoam...

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Autores principales: Ibarra, R., Dazard, J-E., Sandlers, Y., Rehman, F., Abbas, R., Kombu, R., Zhang, G-F., Brunengraber, H., Sanabria, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958765/
https://www.ncbi.nlm.nih.gov/pubmed/24723740
http://dx.doi.org/10.1155/2014/310372
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author Ibarra, R.
Dazard, J-E.
Sandlers, Y.
Rehman, F.
Abbas, R.
Kombu, R.
Zhang, G-F.
Brunengraber, H.
Sanabria, J.
author_facet Ibarra, R.
Dazard, J-E.
Sandlers, Y.
Rehman, F.
Abbas, R.
Kombu, R.
Zhang, G-F.
Brunengraber, H.
Sanabria, J.
author_sort Ibarra, R.
collection PubMed
description Purpose. The incidence of liver neoplasms is rising in USA. The purpose of this study was to determine metabolic profiles of liver tissue during early cancer development. Methods. We used the rabbit VX2 model of liver tumors (LT) and a control group consisting of sham animals implanted with Gelfoam into their livers (LG). After two weeks from implantation, liver tissue from lobes with and without tumor was obtained from experimental animals (LT+/LT−) as well as liver tissue from controls (LG+/LG−). Peaks obtained by Gas Chromatography-Mass Spectrometry were subjected to identification. 56 metabolites were identified and their profiles compared between groups using principal component analysis (PCA) and a mixed-effect two-way ANOVA model. Results. Animals recovered from surgery uneventfully. Analyses identified a metabolite profile that significantly differs in experimental conditions after controlling the False Discovery Rate (FDR). 16 metabolites concentrations differed significantly when comparing samples from (LT+/LT−) to samples from (LG+/LG−) livers. A significant difference was also shown in 20 metabolites when comparing samples from (LT+) liver lobes to samples from (LT−) liver lobes. Conclusion. Normal liver tissue harboring malignancy had a distinct metabolic signature. The role of metabolic profiles on liver biopsies for the detection of early liver cancer remains to be determined.
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spelling pubmed-39587652014-04-10 Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors Ibarra, R. Dazard, J-E. Sandlers, Y. Rehman, F. Abbas, R. Kombu, R. Zhang, G-F. Brunengraber, H. Sanabria, J. HPB Surg Research Article Purpose. The incidence of liver neoplasms is rising in USA. The purpose of this study was to determine metabolic profiles of liver tissue during early cancer development. Methods. We used the rabbit VX2 model of liver tumors (LT) and a control group consisting of sham animals implanted with Gelfoam into their livers (LG). After two weeks from implantation, liver tissue from lobes with and without tumor was obtained from experimental animals (LT+/LT−) as well as liver tissue from controls (LG+/LG−). Peaks obtained by Gas Chromatography-Mass Spectrometry were subjected to identification. 56 metabolites were identified and their profiles compared between groups using principal component analysis (PCA) and a mixed-effect two-way ANOVA model. Results. Animals recovered from surgery uneventfully. Analyses identified a metabolite profile that significantly differs in experimental conditions after controlling the False Discovery Rate (FDR). 16 metabolites concentrations differed significantly when comparing samples from (LT+/LT−) to samples from (LG+/LG−) livers. A significant difference was also shown in 20 metabolites when comparing samples from (LT+) liver lobes to samples from (LT−) liver lobes. Conclusion. Normal liver tissue harboring malignancy had a distinct metabolic signature. The role of metabolic profiles on liver biopsies for the detection of early liver cancer remains to be determined. Hindawi Publishing Corporation 2014 2014-03-02 /pmc/articles/PMC3958765/ /pubmed/24723740 http://dx.doi.org/10.1155/2014/310372 Text en Copyright © 2014 R. Ibarra et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ibarra, R.
Dazard, J-E.
Sandlers, Y.
Rehman, F.
Abbas, R.
Kombu, R.
Zhang, G-F.
Brunengraber, H.
Sanabria, J.
Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title_full Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title_fullStr Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title_full_unstemmed Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title_short Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors
title_sort metabolomic analysis of liver tissue from the vx2 rabbit model of secondary liver tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958765/
https://www.ncbi.nlm.nih.gov/pubmed/24723740
http://dx.doi.org/10.1155/2014/310372
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