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Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas

BACKGROUND: Gene expression is widely used for the characterisation of breast cancers. Variability due to tissue heterogeneity or measurement error or systematic change due to peri-surgical procedures can affect measurements but is poorly documented. We studied the variability of global gene express...

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Autores principales: López-Knowles, Elena, Gao, Qiong, Cheang, Maggie Chon U., Morden, James, Parker, Joel, Martin, Lesley-Ann, Pinhel, Isabel, McNeill, Fiona, Hills, Margaret, Detre, Simone, Afentakis, Maria, Zabaglo, Lila, Dodson, Andrew, Skene, Anthony, Holcombe, Chris, Robertson, John, Smith, Ian, Bliss, Judith M., Dowsett, Mitch
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818440/
https://www.ncbi.nlm.nih.gov/pubmed/27036195
http://dx.doi.org/10.1186/s13058-016-0696-2
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author López-Knowles, Elena
Gao, Qiong
Cheang, Maggie Chon U.
Morden, James
Parker, Joel
Martin, Lesley-Ann
Pinhel, Isabel
McNeill, Fiona
Hills, Margaret
Detre, Simone
Afentakis, Maria
Zabaglo, Lila
Dodson, Andrew
Skene, Anthony
Holcombe, Chris
Robertson, John
Smith, Ian
Bliss, Judith M.
Dowsett, Mitch
author_facet López-Knowles, Elena
Gao, Qiong
Cheang, Maggie Chon U.
Morden, James
Parker, Joel
Martin, Lesley-Ann
Pinhel, Isabel
McNeill, Fiona
Hills, Margaret
Detre, Simone
Afentakis, Maria
Zabaglo, Lila
Dodson, Andrew
Skene, Anthony
Holcombe, Chris
Robertson, John
Smith, Ian
Bliss, Judith M.
Dowsett, Mitch
author_sort López-Knowles, Elena
collection PubMed
description BACKGROUND: Gene expression is widely used for the characterisation of breast cancers. Variability due to tissue heterogeneity or measurement error or systematic change due to peri-surgical procedures can affect measurements but is poorly documented. We studied the variability of global gene expression between core-cuts of primary ER+ breast cancers and the impact of delays to tissue stabilisation due to sample X-ray and of diagnostic core cutting. METHODS: Twenty-six paired core-cuts were taken immediately after tumour excision and up to 90 minutes delay due to sample X-ray; 57 paired core-cuts were taken at diagnosis and 2 weeks later at surgical excision. Whole genome expression analysis was conducted on extracted RNA. Correlations and differences were assessed between the expression of individual genes, gene sets/signatures and intrinsic subtypes. RESULTS: Twenty-three and 56 sample pairs, respectively, were suitable for analysis. The range of correlations for both sample sets were similar with the majority being >0.97 in both. Correlations between pairs for 18 commonly studied genes were also similar between the studies and mainly with Pearson correlation coefficients >0.6 except for a small number of genes, which had a narrow-dynamic range (e.g. MKI67, SNAI2). There was no systematic difference in intrinsic subtyping between the first and second sample of either set but there was c.15 % discordance between the subtype assignments between the pairs, mainly where the subtyping of individual samples was less certain. Increases in the expression of several stress/early-response genes (e.g. FOS, FOSB, JUN) were found in both studies and confirmed findings in earlier smaller studies. Increased expression of IL6, IGFBP2 and MYC (by 17 %, 14 % and 44 %, respectively) occurred between the samples taken 2 weeks apart and again confirmed findings from an earlier study. CONCLUSIONS: There is generally good correlation in gene expression between pairs of core-cuts except where genes have a narrow dynamic range. Similar correlation coefficients to the average gene expression profiles of intrinsic subtype, particularly LumA and LumB, can lead to discordances between assigned subtypes. Substantial changes in expression of early-response genes occur within an hour after surgery and in IL6, IGFB2 and MYC as a result of diagnostic core-cut biopsy. TRIAL REGISTRATION: Trial number CRUK/07/015. Study start date September 2008. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0696-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-48184402016-04-03 Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas López-Knowles, Elena Gao, Qiong Cheang, Maggie Chon U. Morden, James Parker, Joel Martin, Lesley-Ann Pinhel, Isabel McNeill, Fiona Hills, Margaret Detre, Simone Afentakis, Maria Zabaglo, Lila Dodson, Andrew Skene, Anthony Holcombe, Chris Robertson, John Smith, Ian Bliss, Judith M. Dowsett, Mitch Breast Cancer Res Research Article BACKGROUND: Gene expression is widely used for the characterisation of breast cancers. Variability due to tissue heterogeneity or measurement error or systematic change due to peri-surgical procedures can affect measurements but is poorly documented. We studied the variability of global gene expression between core-cuts of primary ER+ breast cancers and the impact of delays to tissue stabilisation due to sample X-ray and of diagnostic core cutting. METHODS: Twenty-six paired core-cuts were taken immediately after tumour excision and up to 90 minutes delay due to sample X-ray; 57 paired core-cuts were taken at diagnosis and 2 weeks later at surgical excision. Whole genome expression analysis was conducted on extracted RNA. Correlations and differences were assessed between the expression of individual genes, gene sets/signatures and intrinsic subtypes. RESULTS: Twenty-three and 56 sample pairs, respectively, were suitable for analysis. The range of correlations for both sample sets were similar with the majority being >0.97 in both. Correlations between pairs for 18 commonly studied genes were also similar between the studies and mainly with Pearson correlation coefficients >0.6 except for a small number of genes, which had a narrow-dynamic range (e.g. MKI67, SNAI2). There was no systematic difference in intrinsic subtyping between the first and second sample of either set but there was c.15 % discordance between the subtype assignments between the pairs, mainly where the subtyping of individual samples was less certain. Increases in the expression of several stress/early-response genes (e.g. FOS, FOSB, JUN) were found in both studies and confirmed findings in earlier smaller studies. Increased expression of IL6, IGFBP2 and MYC (by 17 %, 14 % and 44 %, respectively) occurred between the samples taken 2 weeks apart and again confirmed findings from an earlier study. CONCLUSIONS: There is generally good correlation in gene expression between pairs of core-cuts except where genes have a narrow dynamic range. Similar correlation coefficients to the average gene expression profiles of intrinsic subtype, particularly LumA and LumB, can lead to discordances between assigned subtypes. Substantial changes in expression of early-response genes occur within an hour after surgery and in IL6, IGFB2 and MYC as a result of diagnostic core-cut biopsy. TRIAL REGISTRATION: Trial number CRUK/07/015. Study start date September 2008. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0696-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-01 2016 /pmc/articles/PMC4818440/ /pubmed/27036195 http://dx.doi.org/10.1186/s13058-016-0696-2 Text en © López-Knowles et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
López-Knowles, Elena
Gao, Qiong
Cheang, Maggie Chon U.
Morden, James
Parker, Joel
Martin, Lesley-Ann
Pinhel, Isabel
McNeill, Fiona
Hills, Margaret
Detre, Simone
Afentakis, Maria
Zabaglo, Lila
Dodson, Andrew
Skene, Anthony
Holcombe, Chris
Robertson, John
Smith, Ian
Bliss, Judith M.
Dowsett, Mitch
Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title_full Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title_fullStr Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title_full_unstemmed Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title_short Heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary ER-positive breast carcinomas
title_sort heterogeneity in global gene expression profiles between biopsy specimens taken peri-surgically from primary er-positive breast carcinomas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818440/
https://www.ncbi.nlm.nih.gov/pubmed/27036195
http://dx.doi.org/10.1186/s13058-016-0696-2
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