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Gene expression profiling of peripheral blood cells for early detection of breast cancer

INTRODUCTION: Early detection of breast cancer is key to successful treatment and patient survival. We have previously reported the potential use of gene expression profiling of peripheral blood cells for early detection of breast cancer. The aim of the present study was to refine these findings usi...

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Autores principales: Aarøe, Jørgen, Lindahl, Torbjørn, Dumeaux, Vanessa, Sæbø, Solve, Tobin, Derek, Hagen, Nina, Skaane, Per, Lönneborg, Anders, Sharma, Praveen, Børresen-Dale, Anne-Lise
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880427/
https://www.ncbi.nlm.nih.gov/pubmed/20078854
http://dx.doi.org/10.1186/bcr2472
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author Aarøe, Jørgen
Lindahl, Torbjørn
Dumeaux, Vanessa
Sæbø, Solve
Tobin, Derek
Hagen, Nina
Skaane, Per
Lönneborg, Anders
Sharma, Praveen
Børresen-Dale, Anne-Lise
author_facet Aarøe, Jørgen
Lindahl, Torbjørn
Dumeaux, Vanessa
Sæbø, Solve
Tobin, Derek
Hagen, Nina
Skaane, Per
Lönneborg, Anders
Sharma, Praveen
Børresen-Dale, Anne-Lise
author_sort Aarøe, Jørgen
collection PubMed
description INTRODUCTION: Early detection of breast cancer is key to successful treatment and patient survival. We have previously reported the potential use of gene expression profiling of peripheral blood cells for early detection of breast cancer. The aim of the present study was to refine these findings using a larger sample size and a commercially available microarray platform. METHODS: Blood samples were collected from 121 females referred for diagnostic mammography following an initial suspicious screening mammogram. Diagnostic work-up revealed that 67 of these women had breast cancer while 54 had no malignant disease. Additionally, nine samples from six healthy female controls were included. Gene expression analyses were conducted using high density oligonucleotide microarrays. Partial Least Squares Regression (PLSR) was used for model building while a leave-one-out (LOO) double cross validation approach was used to identify predictors and estimate their prediction efficiency. RESULTS: A set of 738 probes that discriminated breast cancer and non-breast cancer samples was identified. By cross validation we achieved an estimated prediction accuracy of 79.5% with a sensitivity of 80.6% and a specificity of 78.3%. The genes deregulated in blood of breast cancer patients are related to functional processes such as defense response, translation, and various metabolic processes, such as lipid- and steroid metabolism. CONCLUSIONS: We have identified a gene signature in whole blood that classifies breast cancer patients and healthy women with good accuracy supporting our previous findings.
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spelling pubmed-28804272010-06-04 Gene expression profiling of peripheral blood cells for early detection of breast cancer Aarøe, Jørgen Lindahl, Torbjørn Dumeaux, Vanessa Sæbø, Solve Tobin, Derek Hagen, Nina Skaane, Per Lönneborg, Anders Sharma, Praveen Børresen-Dale, Anne-Lise Breast Cancer Res Research article INTRODUCTION: Early detection of breast cancer is key to successful treatment and patient survival. We have previously reported the potential use of gene expression profiling of peripheral blood cells for early detection of breast cancer. The aim of the present study was to refine these findings using a larger sample size and a commercially available microarray platform. METHODS: Blood samples were collected from 121 females referred for diagnostic mammography following an initial suspicious screening mammogram. Diagnostic work-up revealed that 67 of these women had breast cancer while 54 had no malignant disease. Additionally, nine samples from six healthy female controls were included. Gene expression analyses were conducted using high density oligonucleotide microarrays. Partial Least Squares Regression (PLSR) was used for model building while a leave-one-out (LOO) double cross validation approach was used to identify predictors and estimate their prediction efficiency. RESULTS: A set of 738 probes that discriminated breast cancer and non-breast cancer samples was identified. By cross validation we achieved an estimated prediction accuracy of 79.5% with a sensitivity of 80.6% and a specificity of 78.3%. The genes deregulated in blood of breast cancer patients are related to functional processes such as defense response, translation, and various metabolic processes, such as lipid- and steroid metabolism. CONCLUSIONS: We have identified a gene signature in whole blood that classifies breast cancer patients and healthy women with good accuracy supporting our previous findings. BioMed Central 2010 2010-01-15 /pmc/articles/PMC2880427/ /pubmed/20078854 http://dx.doi.org/10.1186/bcr2472 Text en Copyright ©2010 Aarøe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Research article
Aarøe, Jørgen
Lindahl, Torbjørn
Dumeaux, Vanessa
Sæbø, Solve
Tobin, Derek
Hagen, Nina
Skaane, Per
Lönneborg, Anders
Sharma, Praveen
Børresen-Dale, Anne-Lise
Gene expression profiling of peripheral blood cells for early detection of breast cancer
title Gene expression profiling of peripheral blood cells for early detection of breast cancer
title_full Gene expression profiling of peripheral blood cells for early detection of breast cancer
title_fullStr Gene expression profiling of peripheral blood cells for early detection of breast cancer
title_full_unstemmed Gene expression profiling of peripheral blood cells for early detection of breast cancer
title_short Gene expression profiling of peripheral blood cells for early detection of breast cancer
title_sort gene expression profiling of peripheral blood cells for early detection of breast cancer
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880427/
https://www.ncbi.nlm.nih.gov/pubmed/20078854
http://dx.doi.org/10.1186/bcr2472
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