Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Marshall, Harvey E, Foster, Matthew W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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
_version_ 1782320325866815488
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