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Alterations in cellular expression in EBV infected epithelial cell lines and tumors

The Epstein Barr virus (EBV) is linked to the development of two major epithelial malignancies, gastric carcinoma and nasopharyngeal carcinoma. This study evaluates the effects of EBV on cellular expression in a gastric epithelial cell line infected with or without EBV and a nasopharyngeal carcinoma...

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Autores principales: Edwards, Rachel Hood, Dekroon, Robert, Raab-Traub, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795468/
https://www.ncbi.nlm.nih.gov/pubmed/31584998
http://dx.doi.org/10.1371/journal.ppat.1008071
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author Edwards, Rachel Hood
Dekroon, Robert
Raab-Traub, Nancy
author_facet Edwards, Rachel Hood
Dekroon, Robert
Raab-Traub, Nancy
author_sort Edwards, Rachel Hood
collection PubMed
description The Epstein Barr virus (EBV) is linked to the development of two major epithelial malignancies, gastric carcinoma and nasopharyngeal carcinoma. This study evaluates the effects of EBV on cellular expression in a gastric epithelial cell line infected with or without EBV and a nasopharyngeal carcinoma cell line containing EBV. The cells were grown in vitro and as tumors in vivo. The effects on cellular expression were determined using both 2D DIGE proteomics and high throughput RNA sequencing. The data identify multiple pathways that were uniquely activated in vitro. RNA sequences mapping to the mouse genome were identified in both the EBV positive and negative tumor samples in vivo, although, differences between the EBV positive and negative cells were not apparent. However, the tumors appeared to be grossly distinct. The majority of the identified canonical pathways based on two fold changes in expression had decreased activity within the tumors in vivo. Identification of the predicted upstream regulating factors revealed that in vitro the regulating factors were primarily protein transcriptional regulators. In contrast, in vivo the predicted regulators were frequently noncoding RNAs. Hierarchical clustering distinguished the cell lines and tumors, the EBV positive tumors from the EBV negative tumors, and the NPC tumors from the gastric tumors and cell lines. The delineating genes were changed greater than 4 fold and were frequently regulated by protein transcription factors. These data suggest that EBV distinctly affects cellular expression in gastric tumors and NPC and that growth in vivo requires activation of fewer cellular signaling pathways. It is likely that the broad changes in cellular expression that occur at low levels are controlled by regulatory viral and cellular RNAs while major changes are affected by induced protein regulators.
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spelling pubmed-67954682019-10-19 Alterations in cellular expression in EBV infected epithelial cell lines and tumors Edwards, Rachel Hood Dekroon, Robert Raab-Traub, Nancy PLoS Pathog Research Article The Epstein Barr virus (EBV) is linked to the development of two major epithelial malignancies, gastric carcinoma and nasopharyngeal carcinoma. This study evaluates the effects of EBV on cellular expression in a gastric epithelial cell line infected with or without EBV and a nasopharyngeal carcinoma cell line containing EBV. The cells were grown in vitro and as tumors in vivo. The effects on cellular expression were determined using both 2D DIGE proteomics and high throughput RNA sequencing. The data identify multiple pathways that were uniquely activated in vitro. RNA sequences mapping to the mouse genome were identified in both the EBV positive and negative tumor samples in vivo, although, differences between the EBV positive and negative cells were not apparent. However, the tumors appeared to be grossly distinct. The majority of the identified canonical pathways based on two fold changes in expression had decreased activity within the tumors in vivo. Identification of the predicted upstream regulating factors revealed that in vitro the regulating factors were primarily protein transcriptional regulators. In contrast, in vivo the predicted regulators were frequently noncoding RNAs. Hierarchical clustering distinguished the cell lines and tumors, the EBV positive tumors from the EBV negative tumors, and the NPC tumors from the gastric tumors and cell lines. The delineating genes were changed greater than 4 fold and were frequently regulated by protein transcription factors. These data suggest that EBV distinctly affects cellular expression in gastric tumors and NPC and that growth in vivo requires activation of fewer cellular signaling pathways. It is likely that the broad changes in cellular expression that occur at low levels are controlled by regulatory viral and cellular RNAs while major changes are affected by induced protein regulators. Public Library of Science 2019-10-04 /pmc/articles/PMC6795468/ /pubmed/31584998 http://dx.doi.org/10.1371/journal.ppat.1008071 Text en © 2019 Edwards et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Edwards, Rachel Hood
Dekroon, Robert
Raab-Traub, Nancy
Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title_full Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title_fullStr Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title_full_unstemmed Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title_short Alterations in cellular expression in EBV infected epithelial cell lines and tumors
title_sort alterations in cellular expression in ebv infected epithelial cell lines and tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795468/
https://www.ncbi.nlm.nih.gov/pubmed/31584998
http://dx.doi.org/10.1371/journal.ppat.1008071
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