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Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population

Protein expression of Distal-less homeobox 4 (DLX4) was analyzed in inflammatory breast cancer (IBC) cases from an African-American (AA) population to determine if a) DLX4 gene over expression exists in this cohort and b) if the overexpression is associated with breast cancer clinicopathological cha...

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Autores principales: Jeong, Jaehong, Naab, Tammey J., Fernandez, Aileen I., Ongkeko, Martin S., Makambi, Kepher H., Blancato, Jan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101289/
https://www.ncbi.nlm.nih.gov/pubmed/30131852
http://dx.doi.org/10.18632/oncotarget.25790
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author Jeong, Jaehong
Naab, Tammey J.
Fernandez, Aileen I.
Ongkeko, Martin S.
Makambi, Kepher H.
Blancato, Jan K.
author_facet Jeong, Jaehong
Naab, Tammey J.
Fernandez, Aileen I.
Ongkeko, Martin S.
Makambi, Kepher H.
Blancato, Jan K.
author_sort Jeong, Jaehong
collection PubMed
description Protein expression of Distal-less homeobox 4 (DLX4) was analyzed in inflammatory breast cancer (IBC) cases from an African-American (AA) population to determine if a) DLX4 gene over expression exists in this cohort and b) if the overexpression is associated with breast cancer clinicopathological characteristics (ER, PR, HER2, triple-negative). Twenty-nine blocks of formalin-fixed paraffin-embedded (FFPE) tissue from well-characterized human IBC cases were used for immunohistochemical staining (IHC). IHC results were assigned an intensity and percentage score. Percentage scores were assigned as 0, 1, 2, 3, or 4 and intensity scores were assigned 0, 1+, 2+ or 3+. For the analysis of the IHC, a percentage score of 3 or 4 and an intensity score of 2+ or 3+ were categorized as high. Chi-square or Fisher's exact tests were used to compare the high and low groups. In this cohort, 89.7% (26 out of 29) of IBC cases showed high percentages of positive cells staining for the DLX4 protein, while 40.0% (12 out of 30) of normal breast tissue from reduction mammoplasty cases demonstrated DLX4 expression (p < 0.01). In IBC patients, 65.5% of cases showed a high level of staining intensity, compared to 20.0% of normal breast tissues (test, p = 0.001). Intensity to DLX4 was higher in the HER2 negative status (78.3%) than the HER2 positive status (16.7%) (test, p = 0.011). DLX4 expression is higher in the IBC cases in this study of an urban AA population than in normal breast tissue cases. HER2 negative status is positively associated with high intensity of DLX4.
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spelling pubmed-61012892018-08-21 Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population Jeong, Jaehong Naab, Tammey J. Fernandez, Aileen I. Ongkeko, Martin S. Makambi, Kepher H. Blancato, Jan K. Oncotarget Research Paper Protein expression of Distal-less homeobox 4 (DLX4) was analyzed in inflammatory breast cancer (IBC) cases from an African-American (AA) population to determine if a) DLX4 gene over expression exists in this cohort and b) if the overexpression is associated with breast cancer clinicopathological characteristics (ER, PR, HER2, triple-negative). Twenty-nine blocks of formalin-fixed paraffin-embedded (FFPE) tissue from well-characterized human IBC cases were used for immunohistochemical staining (IHC). IHC results were assigned an intensity and percentage score. Percentage scores were assigned as 0, 1, 2, 3, or 4 and intensity scores were assigned 0, 1+, 2+ or 3+. For the analysis of the IHC, a percentage score of 3 or 4 and an intensity score of 2+ or 3+ were categorized as high. Chi-square or Fisher's exact tests were used to compare the high and low groups. In this cohort, 89.7% (26 out of 29) of IBC cases showed high percentages of positive cells staining for the DLX4 protein, while 40.0% (12 out of 30) of normal breast tissue from reduction mammoplasty cases demonstrated DLX4 expression (p < 0.01). In IBC patients, 65.5% of cases showed a high level of staining intensity, compared to 20.0% of normal breast tissues (test, p = 0.001). Intensity to DLX4 was higher in the HER2 negative status (78.3%) than the HER2 positive status (16.7%) (test, p = 0.011). DLX4 expression is higher in the IBC cases in this study of an urban AA population than in normal breast tissue cases. HER2 negative status is positively associated with high intensity of DLX4. Impact Journals LLC 2018-07-27 /pmc/articles/PMC6101289/ /pubmed/30131852 http://dx.doi.org/10.18632/oncotarget.25790 Text en Copyright: © 2018 Jeong et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Jeong, Jaehong
Naab, Tammey J.
Fernandez, Aileen I.
Ongkeko, Martin S.
Makambi, Kepher H.
Blancato, Jan K.
Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title_full Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title_fullStr Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title_full_unstemmed Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title_short Homeoprotein DLX4 expression is increased in inflammatory breast cancer cases from an urban African-American population
title_sort homeoprotein dlx4 expression is increased in inflammatory breast cancer cases from an urban african-american population
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101289/
https://www.ncbi.nlm.nih.gov/pubmed/30131852
http://dx.doi.org/10.18632/oncotarget.25790
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