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Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways
Oncolytic viruses exploit alterations in cancer cells to specifically infect cancer cells but not normal healthy cells. Previous work has shown that oncogenic Ras interferes with interferon (IFN) signaling to promote viral replication. Furthermore, inhibition of the Ras/Raf/MEK/ERK pathway at the le...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535867/ https://www.ncbi.nlm.nih.gov/pubmed/26484185 http://dx.doi.org/10.1016/j.gdata.2015.03.012 |
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author | Komatsu, Y. Hirasawa, K. Christian, S.L. |
author_facet | Komatsu, Y. Hirasawa, K. Christian, S.L. |
author_sort | Komatsu, Y. |
collection | PubMed |
description | Oncolytic viruses exploit alterations in cancer cells to specifically infect cancer cells but not normal healthy cells. Previous work has shown that oncogenic Ras interferes with interferon (IFN) signaling to promote viral replication. Furthermore, inhibition of the Ras/Raf/MEK/ERK pathway at the level of Ras, MEK, or ERK was sufficient to restore IFN signaling. In order to identify genes that were commonly regulated by the inhibition of the Ras pathway and the IFN pathway, we treated NIH/3T3 cells that overexpress oncogenic Ras with the MEK inhibitor, U0126, or IFN-α for 6 h, and performed DNA microarray analysis (Gene Expression Omnibus accession number GSE49469). Here, we also provide additional information on the experimental and functional analysis of the genes responsive to U0126 and IFN. |
format | Online Article Text |
id | pubmed-4535867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45358672015-10-19 Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways Komatsu, Y. Hirasawa, K. Christian, S.L. Genom Data Data in Brief Oncolytic viruses exploit alterations in cancer cells to specifically infect cancer cells but not normal healthy cells. Previous work has shown that oncogenic Ras interferes with interferon (IFN) signaling to promote viral replication. Furthermore, inhibition of the Ras/Raf/MEK/ERK pathway at the level of Ras, MEK, or ERK was sufficient to restore IFN signaling. In order to identify genes that were commonly regulated by the inhibition of the Ras pathway and the IFN pathway, we treated NIH/3T3 cells that overexpress oncogenic Ras with the MEK inhibitor, U0126, or IFN-α for 6 h, and performed DNA microarray analysis (Gene Expression Omnibus accession number GSE49469). Here, we also provide additional information on the experimental and functional analysis of the genes responsive to U0126 and IFN. Elsevier 2015-04-03 /pmc/articles/PMC4535867/ /pubmed/26484185 http://dx.doi.org/10.1016/j.gdata.2015.03.012 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Data in Brief Komatsu, Y. Hirasawa, K. Christian, S.L. Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title | Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title_full | Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title_fullStr | Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title_full_unstemmed | Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title_short | Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways |
title_sort | global gene analysis identifying genes commonly regulated by the ras/raf/mek and type i ifn pathways |
topic | Data in Brief |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535867/ https://www.ncbi.nlm.nih.gov/pubmed/26484185 http://dx.doi.org/10.1016/j.gdata.2015.03.012 |
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