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S-nitrosylation of Ras in breast cancer
Elevated expression of nitric oxide synthase 2 has been recently shown to correlate with poor survival in estrogen receptor-negative breast cancer. In an article in Breast Cancer Research, Switzer and colleagues identify the transcription factor Ets-1 as a critical mediator of nitric oxide-dependent...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053123/ https://www.ncbi.nlm.nih.gov/pubmed/23167903 http://dx.doi.org/10.1186/bcr3331 |
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author | Marshall, Harvey E Foster, Matthew W |
author_facet | Marshall, Harvey E Foster, Matthew W |
author_sort | Marshall, Harvey E |
collection | PubMed |
description | Elevated expression of nitric oxide synthase 2 has been recently shown to correlate with poor survival in estrogen receptor-negative breast cancer. In an article in Breast Cancer Research, Switzer and colleagues identify the transcription factor Ets-1 as a critical mediator of nitric oxide-dependent oncogenic gene expression in basal-like breast cancer. This pathway is driven by S-nitrosylation of wild-type Ras, which leads to mitogen-activated protein kinase-dependent phosphorylation and activation of Ets-1. These results establish a new role for S-nitrosylation in mediating an aggressive breast cancer phenotype. |
format | Online Article Text |
id | pubmed-4053123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40531232014-06-12 S-nitrosylation of Ras in breast cancer Marshall, Harvey E Foster, Matthew W Breast Cancer Res Editorial Elevated expression of nitric oxide synthase 2 has been recently shown to correlate with poor survival in estrogen receptor-negative breast cancer. In an article in Breast Cancer Research, Switzer and colleagues identify the transcription factor Ets-1 as a critical mediator of nitric oxide-dependent oncogenic gene expression in basal-like breast cancer. This pathway is driven by S-nitrosylation of wild-type Ras, which leads to mitogen-activated protein kinase-dependent phosphorylation and activation of Ets-1. These results establish a new role for S-nitrosylation in mediating an aggressive breast cancer phenotype. BioMed Central 2012 2012-11-12 /pmc/articles/PMC4053123/ /pubmed/23167903 http://dx.doi.org/10.1186/bcr3331 Text en Copyright © 2012 BioMed Central Ltd. |
spellingShingle | Editorial Marshall, Harvey E Foster, Matthew W S-nitrosylation of Ras in breast cancer |
title | S-nitrosylation of Ras in breast cancer |
title_full | S-nitrosylation of Ras in breast cancer |
title_fullStr | S-nitrosylation of Ras in breast cancer |
title_full_unstemmed | S-nitrosylation of Ras in breast cancer |
title_short | S-nitrosylation of Ras in breast cancer |
title_sort | s-nitrosylation of ras in breast cancer |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053123/ https://www.ncbi.nlm.nih.gov/pubmed/23167903 http://dx.doi.org/10.1186/bcr3331 |
work_keys_str_mv | AT marshallharveye snitrosylationofrasinbreastcancer AT fostermattheww snitrosylationofrasinbreastcancer |