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Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice
This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT(664V-E )mice). The Ingenuity knowledge database was used to characteri...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206718/ https://www.ncbi.nlm.nih.gov/pubmed/17705881 http://dx.doi.org/10.1186/bcr1745 |
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author | Calogero, Raffaele Adolfo Cordero, Francesca Forni, Guido Cavallo, Federica |
author_facet | Calogero, Raffaele Adolfo Cordero, Francesca Forni, Guido Cavallo, Federica |
author_sort | Calogero, Raffaele Adolfo |
collection | PubMed |
description | This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT(664V-E )mice). The Ingenuity knowledge database was used to characterize four functional association networks whose hub genes are directly linked to inflammation (specifically, the genes encoding IL-1β, tumour necrosis factor, interferon-γ, and monocyte chemoattractant protein-1/CC chemokine ligand-2) and are increasingly expressed during such progression. In silico meta-analysis in a human breast cancer dataset suggests that proinflammatory activation in the mammary glands of these mice reflects a general pattern of human breast cancer. |
format | Text |
id | pubmed-2206718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22067182008-01-19 Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice Calogero, Raffaele Adolfo Cordero, Francesca Forni, Guido Cavallo, Federica Breast Cancer Res Review This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT(664V-E )mice). The Ingenuity knowledge database was used to characterize four functional association networks whose hub genes are directly linked to inflammation (specifically, the genes encoding IL-1β, tumour necrosis factor, interferon-γ, and monocyte chemoattractant protein-1/CC chemokine ligand-2) and are increasingly expressed during such progression. In silico meta-analysis in a human breast cancer dataset suggests that proinflammatory activation in the mammary glands of these mice reflects a general pattern of human breast cancer. BioMed Central 2007 2007-08-10 /pmc/articles/PMC2206718/ /pubmed/17705881 http://dx.doi.org/10.1186/bcr1745 Text en Copyright © 2007 BioMed Central Ltd |
spellingShingle | Review Calogero, Raffaele Adolfo Cordero, Francesca Forni, Guido Cavallo, Federica Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title | Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title_full | Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title_fullStr | Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title_full_unstemmed | Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title_short | Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice |
title_sort | inflammation and breast cancer. inflammatory component of mammary carcinogenesis in erbb2 transgenic mice |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206718/ https://www.ncbi.nlm.nih.gov/pubmed/17705881 http://dx.doi.org/10.1186/bcr1745 |
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