Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis

<p>Abstract</p> <p>Breast cancer tumours among African Americans are usually more aggressive than those found in Caucasian populations. African-American patients with breast cancer also have higher mortality rates than Caucasian women. A better understanding of the disease aetiolog...

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Main Authors: Pang Herbert, Ebisu Keita, Watanabe Emi, Sue Laura Y, Tong Tiejun
Format: Article
Language:English
Published: BMC 2010-10-01
Series:Human Genomics
Subjects:
Online Access:http://www.humgenomics.com/content/5/1/5
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author Pang Herbert
Ebisu Keita
Watanabe Emi
Sue Laura Y
Tong Tiejun
author_facet Pang Herbert
Ebisu Keita
Watanabe Emi
Sue Laura Y
Tong Tiejun
author_sort Pang Herbert
collection DOAJ
description <p>Abstract</p> <p>Breast cancer tumours among African Americans are usually more aggressive than those found in Caucasian populations. African-American patients with breast cancer also have higher mortality rates than Caucasian women. A better understanding of the disease aetiology of these breast cancers can help to improve and develop new methods for cancer prevention, diagnosis and treatment. The main goal of this project was to identify genes that help differentiate between oestrogen receptor-positive and -negative samples among a small group of African-American patients with breast cancer. Breast cancer microarrays from one of the largest genomic consortiums were analysed using 13 African-American and 201 Caucasian samples with oestrogen receptor status. We used a shrinkage-based classification method to identify genes that were informative in discriminating between oestrogen receptor-positive and -negative samples. Subset analysis and permutation were performed to obtain a set of genes unique to the African-American population. We identified a set of 156 probe sets, which gave a misclassification rate of 0.16 in distinguishing between oestrogen receptor-positive and -negative patients. The biological relevance of our findings was explored through literature-mining techniques and pathway mapping. An independent dataset was used to validate our findings and we found that the top ten genes mapped onto this dataset gave a misclassification rate of 0.15. The described method allows us best to utilise the information available from small sample size microarray data in the context of ethnic minorities.</p>
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spelling doaj.art-1cd0b73e7a5d47c3ab8321e03ed5b4482022-12-22T03:59:53ZengBMCHuman Genomics1479-73642010-10-015151610.1186/1479-7364-5-1-5Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysisPang HerbertEbisu KeitaWatanabe EmiSue Laura YTong Tiejun<p>Abstract</p> <p>Breast cancer tumours among African Americans are usually more aggressive than those found in Caucasian populations. African-American patients with breast cancer also have higher mortality rates than Caucasian women. A better understanding of the disease aetiology of these breast cancers can help to improve and develop new methods for cancer prevention, diagnosis and treatment. The main goal of this project was to identify genes that help differentiate between oestrogen receptor-positive and -negative samples among a small group of African-American patients with breast cancer. Breast cancer microarrays from one of the largest genomic consortiums were analysed using 13 African-American and 201 Caucasian samples with oestrogen receptor status. We used a shrinkage-based classification method to identify genes that were informative in discriminating between oestrogen receptor-positive and -negative samples. Subset analysis and permutation were performed to obtain a set of genes unique to the African-American population. We identified a set of 156 probe sets, which gave a misclassification rate of 0.16 in distinguishing between oestrogen receptor-positive and -negative patients. The biological relevance of our findings was explored through literature-mining techniques and pathway mapping. An independent dataset was used to validate our findings and we found that the top ten genes mapped onto this dataset gave a misclassification rate of 0.15. The described method allows us best to utilise the information available from small sample size microarray data in the context of ethnic minorities.</p>http://www.humgenomics.com/content/5/1/5African Americansbreast cancerdiscriminant analysisoestrogen receptorhealth disparitiesmicroarrays
spellingShingle Pang Herbert
Ebisu Keita
Watanabe Emi
Sue Laura Y
Tong Tiejun
Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
Human Genomics
African Americans
breast cancer
discriminant analysis
oestrogen receptor
health disparities
microarrays
title Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
title_full Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
title_fullStr Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
title_full_unstemmed Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
title_short Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
title_sort analysing breast cancer microarrays from african americans using shrinkage based discriminant analysis
topic African Americans
breast cancer
discriminant analysis
oestrogen receptor
health disparities
microarrays
url http://www.humgenomics.com/content/5/1/5
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AT watanabeemi analysingbreastcancermicroarraysfromafricanamericansusingshrinkagebaseddiscriminantanalysis
AT suelauray analysingbreastcancermicroarraysfromafricanamericansusingshrinkagebaseddiscriminantanalysis
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