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Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia
Background: Using immunohistochemical stains to target specific breast cancer markers has become indispensable for evaluation of small diagnostic tissue specimens, and therefore novel marker cocktails for specific breast cancers are required. This study was conducted to assess the immunoexpression o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820604/ https://www.ncbi.nlm.nih.gov/pubmed/29527291 http://dx.doi.org/10.12688/f1000research.12671.2 |
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author | Kamarlis, Reno K Lubis, Muhammad ND Hernowo, Bethy S Kar, Azmi S |
author_facet | Kamarlis, Reno K Lubis, Muhammad ND Hernowo, Bethy S Kar, Azmi S |
author_sort | Kamarlis, Reno K |
collection | PubMed |
description | Background: Using immunohistochemical stains to target specific breast cancer markers has become indispensable for evaluation of small diagnostic tissue specimens, and therefore novel marker cocktails for specific breast cancers are required. This study was conducted to assess the immunoexpression of P63 and SOX2 in triple negative breast cancer (TNBC), and to evaluate the predictive diagnostic value of these markers for specific types of TNBC. Methods: Histological slides and paraffin blocks of TNBC cases were collected from Dr. Hasan Sadikin Hospital, Bandung, Indonesia from 5-years period (2011-2015). Each histological slide was subjected to immunohistochemical staining for P63 (nucleus and cytoplasm) and SOX2 (nucleus), with specific primer antibodies. Immunoexpression of P63 and SOX2 was evaluated using immunoreactivity scoring. Associations between P63 and SOX2 immunoexpression and TNBC types were assessed using Mann Whitney tests. In addition, the predictive diagnostic values of these markers were assessed. Results: Forty TNBC histological slides were included, and 23 (57.5%) were Basal-like type TNBC and 17 (42.5%) were Non basal-like type TNBC. Immunoexpression of P63 nucleus and SOX2 was not different between types of TNBC. However, immunoexpression of P63 in the cytoplasm in Basal-like type TNBC was significantly higher than in Non basal-like type TNBC ( p=0.021). Predictor diagnostic value analysis suggested that immunoexpression of P63 in cytoplasm had 56.5% sensitivity and 70.6% specificity for diagnosing Basal-like type TNBC, with area under curve of 0.64. Conclusions: Immunoexpression of P63 in the cytoplasm has a relatively weak diagnostic value to discriminate Basal-like and Non basal-like types of TNBC. |
format | Online Article Text |
id | pubmed-5820604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-58206042018-03-08 Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia Kamarlis, Reno K Lubis, Muhammad ND Hernowo, Bethy S Kar, Azmi S F1000Res Research Article Background: Using immunohistochemical stains to target specific breast cancer markers has become indispensable for evaluation of small diagnostic tissue specimens, and therefore novel marker cocktails for specific breast cancers are required. This study was conducted to assess the immunoexpression of P63 and SOX2 in triple negative breast cancer (TNBC), and to evaluate the predictive diagnostic value of these markers for specific types of TNBC. Methods: Histological slides and paraffin blocks of TNBC cases were collected from Dr. Hasan Sadikin Hospital, Bandung, Indonesia from 5-years period (2011-2015). Each histological slide was subjected to immunohistochemical staining for P63 (nucleus and cytoplasm) and SOX2 (nucleus), with specific primer antibodies. Immunoexpression of P63 and SOX2 was evaluated using immunoreactivity scoring. Associations between P63 and SOX2 immunoexpression and TNBC types were assessed using Mann Whitney tests. In addition, the predictive diagnostic values of these markers were assessed. Results: Forty TNBC histological slides were included, and 23 (57.5%) were Basal-like type TNBC and 17 (42.5%) were Non basal-like type TNBC. Immunoexpression of P63 nucleus and SOX2 was not different between types of TNBC. However, immunoexpression of P63 in the cytoplasm in Basal-like type TNBC was significantly higher than in Non basal-like type TNBC ( p=0.021). Predictor diagnostic value analysis suggested that immunoexpression of P63 in cytoplasm had 56.5% sensitivity and 70.6% specificity for diagnosing Basal-like type TNBC, with area under curve of 0.64. Conclusions: Immunoexpression of P63 in the cytoplasm has a relatively weak diagnostic value to discriminate Basal-like and Non basal-like types of TNBC. F1000 Research Limited 2018-01-08 /pmc/articles/PMC5820604/ /pubmed/29527291 http://dx.doi.org/10.12688/f1000research.12671.2 Text en Copyright: © 2018 Kamarlis RK et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kamarlis, Reno K Lubis, Muhammad ND Hernowo, Bethy S Kar, Azmi S Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title | Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title_full | Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title_fullStr | Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title_full_unstemmed | Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title_short | Immunoexpression of P63 and SOX2 in triple-negative breast cancers, Indonesia |
title_sort | immunoexpression of p63 and sox2 in triple-negative breast cancers, indonesia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820604/ https://www.ncbi.nlm.nih.gov/pubmed/29527291 http://dx.doi.org/10.12688/f1000research.12671.2 |
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