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Gene expression profiling of calcifications in breast cancer

We investigated the gene expression profiles of calcifications in breast cancer. Gene expression analysis of surgical specimen was performed using Affymetrix GeneChip® Human Gene 2.0 ST arrays in 168 breast cancer patients. The mammographic calcifications were reviewed by three radiologists and clas...

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Autores principales: Shin, Sung Ui, Lee, Jeonghoon, Kim, Ju Han, Kim, Won Hwa, Song, Sung Eun, Chu, Ajung, Kim, Hoe Suk, Han, Wonshik, Ryu, Han Suk, Moon, Woo Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595962/
https://www.ncbi.nlm.nih.gov/pubmed/28900139
http://dx.doi.org/10.1038/s41598-017-11331-9
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author Shin, Sung Ui
Lee, Jeonghoon
Kim, Ju Han
Kim, Won Hwa
Song, Sung Eun
Chu, Ajung
Kim, Hoe Suk
Han, Wonshik
Ryu, Han Suk
Moon, Woo Kyung
author_facet Shin, Sung Ui
Lee, Jeonghoon
Kim, Ju Han
Kim, Won Hwa
Song, Sung Eun
Chu, Ajung
Kim, Hoe Suk
Han, Wonshik
Ryu, Han Suk
Moon, Woo Kyung
author_sort Shin, Sung Ui
collection PubMed
description We investigated the gene expression profiles of calcifications in breast cancer. Gene expression analysis of surgical specimen was performed using Affymetrix GeneChip® Human Gene 2.0 ST arrays in 168 breast cancer patients. The mammographic calcifications were reviewed by three radiologists and classified into three groups according to malignancy probability: breast cancers without suspicious calcifications; breast cancers with low-to-intermediate suspicious calcifications; and breast cancers with highly suspicious calcifications. To identify differentially expressed genes (DEGs) between these three groups, a one-way analysis of variance was performed with post hoc comparisons with Tukey’s honest significant difference test. To explore the biological significance of DEGs, we used DAVID for gene ontology analysis and BioLattice for clustering analysis. A total of 2551 genes showed differential expression among the three groups. ERBB2 genes are up-regulated in breast cancers with highly suspicious calcifications (fold change 2.474, p < 0.001). Gene ontology analysis revealed that the immune, defense and inflammatory responses were decreased in breast cancers with highly suspicious calcifications compared to breast cancers without suspicious calcifications (p from 10(−23) to 10(−8)). The clustering analysis also demonstrated that the immune system is associated with mammographic calcifications (p < 0.001). Our study showed calcifications in breast cancers are associated with high levels of mRNA expression of ERBB2 and decreased immune system activity.
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spelling pubmed-55959622017-09-15 Gene expression profiling of calcifications in breast cancer Shin, Sung Ui Lee, Jeonghoon Kim, Ju Han Kim, Won Hwa Song, Sung Eun Chu, Ajung Kim, Hoe Suk Han, Wonshik Ryu, Han Suk Moon, Woo Kyung Sci Rep Article We investigated the gene expression profiles of calcifications in breast cancer. Gene expression analysis of surgical specimen was performed using Affymetrix GeneChip® Human Gene 2.0 ST arrays in 168 breast cancer patients. The mammographic calcifications were reviewed by three radiologists and classified into three groups according to malignancy probability: breast cancers without suspicious calcifications; breast cancers with low-to-intermediate suspicious calcifications; and breast cancers with highly suspicious calcifications. To identify differentially expressed genes (DEGs) between these three groups, a one-way analysis of variance was performed with post hoc comparisons with Tukey’s honest significant difference test. To explore the biological significance of DEGs, we used DAVID for gene ontology analysis and BioLattice for clustering analysis. A total of 2551 genes showed differential expression among the three groups. ERBB2 genes are up-regulated in breast cancers with highly suspicious calcifications (fold change 2.474, p < 0.001). Gene ontology analysis revealed that the immune, defense and inflammatory responses were decreased in breast cancers with highly suspicious calcifications compared to breast cancers without suspicious calcifications (p from 10(−23) to 10(−8)). The clustering analysis also demonstrated that the immune system is associated with mammographic calcifications (p < 0.001). Our study showed calcifications in breast cancers are associated with high levels of mRNA expression of ERBB2 and decreased immune system activity. Nature Publishing Group UK 2017-09-12 /pmc/articles/PMC5595962/ /pubmed/28900139 http://dx.doi.org/10.1038/s41598-017-11331-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shin, Sung Ui
Lee, Jeonghoon
Kim, Ju Han
Kim, Won Hwa
Song, Sung Eun
Chu, Ajung
Kim, Hoe Suk
Han, Wonshik
Ryu, Han Suk
Moon, Woo Kyung
Gene expression profiling of calcifications in breast cancer
title Gene expression profiling of calcifications in breast cancer
title_full Gene expression profiling of calcifications in breast cancer
title_fullStr Gene expression profiling of calcifications in breast cancer
title_full_unstemmed Gene expression profiling of calcifications in breast cancer
title_short Gene expression profiling of calcifications in breast cancer
title_sort gene expression profiling of calcifications in breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595962/
https://www.ncbi.nlm.nih.gov/pubmed/28900139
http://dx.doi.org/10.1038/s41598-017-11331-9
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