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Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma

AIMS: Fos-related antigen 1 (Fra-1) is a member of the activator protein 1 (AP-1) transcription factor family. Our objective was to evaluate the role of Fra-1 expression in breast carcinoma progression and prognosis. METHODS AND RESULTS: Fra-1 expression was investigated by immunohistochemistry in t...

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Autores principales: Logullo, Angela Flavia, Stiepcich, Mônica Maria Ágata, de Toledo Osório, Cintia Aparecida Bueno, Nonogaki, Sueli, Pasini, Fátima Solange, Rocha, Rafael Malagoli, Soares, Fernando Augusto, Brentani, Maria M
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085077/
https://www.ncbi.nlm.nih.gov/pubmed/21371080
http://dx.doi.org/10.1111/j.1365-2559.2011.03785.x
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author Logullo, Angela Flavia
Stiepcich, Mônica Maria Ágata
de Toledo Osório, Cintia Aparecida Bueno
Nonogaki, Sueli
Pasini, Fátima Solange
Rocha, Rafael Malagoli
Soares, Fernando Augusto
Brentani, Maria M
author_facet Logullo, Angela Flavia
Stiepcich, Mônica Maria Ágata
de Toledo Osório, Cintia Aparecida Bueno
Nonogaki, Sueli
Pasini, Fátima Solange
Rocha, Rafael Malagoli
Soares, Fernando Augusto
Brentani, Maria M
author_sort Logullo, Angela Flavia
collection PubMed
description AIMS: Fos-related antigen 1 (Fra-1) is a member of the activator protein 1 (AP-1) transcription factor family. Our objective was to evaluate the role of Fra-1 expression in breast carcinoma progression and prognosis. METHODS AND RESULTS: Fra-1 expression was investigated by immunohistochemistry in two tissue microarrays containing, respectively, 85 ductal carcinoma in situ (DCIS) and 771 invasive ductal carcinoma (IDC) samples. Staining was observed in the nucleus and cytoplasm of the carcinomas, but only nuclear staining was considered to be positive. Fibroblasts associated with IDC were also Fra-1-positive. The frequency of Fra-1 positivity in IDC (22.8%) was lower than that in DCIS (42.2%). No association was found between Fra-1 and clinico-pathological variables in DCIS. In IDC, Fra-1 expression correlated with aggressive phenotype markers, including: high grade, oestrogen receptor negativity and human epidermal growth factor receptor 2 (HER-2) positivity (P = 0.001, 0.015 and 0.004, respectively), and marginally with the presence of metastasis (P = 0.07). Fra-1 was more frequently positive in basal-like (34%) and in HER-2-positive (38.5%) subtypes than in luminal subtypes. Fra-1 presence did not correlate with survival. CONCLUSIONS: A high frequency of Fra-1 in DCIS tumours may be associated with early events in breast carcinogenesis. Although Fra-1 expression correlated with features of a more aggressive phenotype in IDC, no relationship with overall survival was found.
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spelling pubmed-30850772011-05-13 Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma Logullo, Angela Flavia Stiepcich, Mônica Maria Ágata de Toledo Osório, Cintia Aparecida Bueno Nonogaki, Sueli Pasini, Fátima Solange Rocha, Rafael Malagoli Soares, Fernando Augusto Brentani, Maria M Histopathology Original Articles AIMS: Fos-related antigen 1 (Fra-1) is a member of the activator protein 1 (AP-1) transcription factor family. Our objective was to evaluate the role of Fra-1 expression in breast carcinoma progression and prognosis. METHODS AND RESULTS: Fra-1 expression was investigated by immunohistochemistry in two tissue microarrays containing, respectively, 85 ductal carcinoma in situ (DCIS) and 771 invasive ductal carcinoma (IDC) samples. Staining was observed in the nucleus and cytoplasm of the carcinomas, but only nuclear staining was considered to be positive. Fibroblasts associated with IDC were also Fra-1-positive. The frequency of Fra-1 positivity in IDC (22.8%) was lower than that in DCIS (42.2%). No association was found between Fra-1 and clinico-pathological variables in DCIS. In IDC, Fra-1 expression correlated with aggressive phenotype markers, including: high grade, oestrogen receptor negativity and human epidermal growth factor receptor 2 (HER-2) positivity (P = 0.001, 0.015 and 0.004, respectively), and marginally with the presence of metastasis (P = 0.07). Fra-1 was more frequently positive in basal-like (34%) and in HER-2-positive (38.5%) subtypes than in luminal subtypes. Fra-1 presence did not correlate with survival. CONCLUSIONS: A high frequency of Fra-1 in DCIS tumours may be associated with early events in breast carcinogenesis. Although Fra-1 expression correlated with features of a more aggressive phenotype in IDC, no relationship with overall survival was found. Blackwell Publishing Ltd 2011-03 /pmc/articles/PMC3085077/ /pubmed/21371080 http://dx.doi.org/10.1111/j.1365-2559.2011.03785.x Text en Copyright © 2011 Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Logullo, Angela Flavia
Stiepcich, Mônica Maria Ágata
de Toledo Osório, Cintia Aparecida Bueno
Nonogaki, Sueli
Pasini, Fátima Solange
Rocha, Rafael Malagoli
Soares, Fernando Augusto
Brentani, Maria M
Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title_full Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title_fullStr Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title_full_unstemmed Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title_short Role of Fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
title_sort role of fos-related antigen 1 in the progression and prognosis of ductal breast carcinoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085077/
https://www.ncbi.nlm.nih.gov/pubmed/21371080
http://dx.doi.org/10.1111/j.1365-2559.2011.03785.x
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