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Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways
BACKGROUND: Cervical carcinoma (CC) is a leading cause of death among women worldwide. Human papilloma virus (HPV) is a major etiological factor in CC and HPV 16 is the more frequent viral type present. Our aim was to characterize metabolic pathways altered in HPV 16 tumor samples by means of transc...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034543/ https://www.ncbi.nlm.nih.gov/pubmed/17822553 http://dx.doi.org/10.1186/1750-9378-2-16 |
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author | Pérez-Plasencia, Carlos Vázquez-Ortiz, Guelaguetza López-Romero, Ricardo Piña-Sanchez, Patricia Moreno, José Salcedo, Mauricio |
author_facet | Pérez-Plasencia, Carlos Vázquez-Ortiz, Guelaguetza López-Romero, Ricardo Piña-Sanchez, Patricia Moreno, José Salcedo, Mauricio |
author_sort | Pérez-Plasencia, Carlos |
collection | PubMed |
description | BACKGROUND: Cervical carcinoma (CC) is a leading cause of death among women worldwide. Human papilloma virus (HPV) is a major etiological factor in CC and HPV 16 is the more frequent viral type present. Our aim was to characterize metabolic pathways altered in HPV 16 tumor samples by means of transcriptome wide analysis and bioinformatics tools for visualizing expression data in the context of KEGG biological pathways. RESULTS: We found 2,067 genes significantly up or down-modulated (at least 2-fold) in tumor clinical samples compared to normal tissues, representing ~3.7% of analyzed genes. Cervical carcinoma was associated with an important up-regulation of Wnt signaling pathway, which was validated by in situ hybridization in clinical samples. Other up-regulated pathways were those of calcium signaling and MAPK signaling, as well as cell cycle-related genes. There was down-regulation of focal adhesion, TGF-β signaling, among other metabolic pathways. CONCLUSION: This analysis of HPV 16 tumors transcriptome could be useful for the identification of genes and molecular pathways involved in the pathogenesis of cervical carcinoma. Understanding the possible role of these proteins in the pathogenesis of CC deserves further studies. |
format | Text |
id | pubmed-2034543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20345432007-10-19 Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways Pérez-Plasencia, Carlos Vázquez-Ortiz, Guelaguetza López-Romero, Ricardo Piña-Sanchez, Patricia Moreno, José Salcedo, Mauricio Infect Agent Cancer Research Article BACKGROUND: Cervical carcinoma (CC) is a leading cause of death among women worldwide. Human papilloma virus (HPV) is a major etiological factor in CC and HPV 16 is the more frequent viral type present. Our aim was to characterize metabolic pathways altered in HPV 16 tumor samples by means of transcriptome wide analysis and bioinformatics tools for visualizing expression data in the context of KEGG biological pathways. RESULTS: We found 2,067 genes significantly up or down-modulated (at least 2-fold) in tumor clinical samples compared to normal tissues, representing ~3.7% of analyzed genes. Cervical carcinoma was associated with an important up-regulation of Wnt signaling pathway, which was validated by in situ hybridization in clinical samples. Other up-regulated pathways were those of calcium signaling and MAPK signaling, as well as cell cycle-related genes. There was down-regulation of focal adhesion, TGF-β signaling, among other metabolic pathways. CONCLUSION: This analysis of HPV 16 tumors transcriptome could be useful for the identification of genes and molecular pathways involved in the pathogenesis of cervical carcinoma. Understanding the possible role of these proteins in the pathogenesis of CC deserves further studies. BioMed Central 2007-09-06 /pmc/articles/PMC2034543/ /pubmed/17822553 http://dx.doi.org/10.1186/1750-9378-2-16 Text en Copyright © 2007 Pérez-Plasencia et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pérez-Plasencia, Carlos Vázquez-Ortiz, Guelaguetza López-Romero, Ricardo Piña-Sanchez, Patricia Moreno, José Salcedo, Mauricio Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title | Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title_full | Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title_fullStr | Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title_full_unstemmed | Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title_short | Genome wide expression analysis in HPV16 Cervical Cancer: identification of altered metabolic pathways |
title_sort | genome wide expression analysis in hpv16 cervical cancer: identification of altered metabolic pathways |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034543/ https://www.ncbi.nlm.nih.gov/pubmed/17822553 http://dx.doi.org/10.1186/1750-9378-2-16 |
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