Prognostic value of follistatin-like 3 in human invasive breast cancer
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFMG |
Texto Completo: | https://doi.org/10.18632/oncotarget.15026 http://hdl.handle.net/1843/59238 https://orcid.org/0000-0002-0873-8160 https://orcid.org/0000-0002-8442-8797 https://orcid.org/0000-0001-7972-720X https://orcid.org/0000-0003-0275-8686 https://orcid.org/0000-0002-8227-7972 |
Resumo: | Follistatin-like 3 (FSTL3) binds and inactivates activin, a growth factor involved with cell growth and differentiation. We have previously shown FSTL3 overexpression in invasive breast cancers, but its clinical relevance remained unexplored. Here we evaluate FSTL3 as a prognostic tool and its relation with clinical and pathological features of breast cancer. A cohort of 154 women diagnosed with invasive breast cancer between 2008 and 2012 was followed up for 5 years. Tumor samples were processed by immunohistochemistry to detect FSTL3 expression in tumor epithelium. FSTL3 expression was classified semiquantitatively and tested for possible correlation with age, menopause status, stage, tumor histological type and grade, estrogen receptor, progesterone receptor, and HER2 expression. Survival plots with Kaplan-Mayer statistics were used to assess whether FSTL3 expression predicted disease-free survival. Our findings show that FSTL3 staining was unrelated to menopausal status, histological type, disease stage, or receptor profile. However, the intensity of FSTL3 immunostaining correlated inversely with tumor size (r = -0.366, p<0.001) and with nuclear grade (p<0.01). The intensity of FSTL3 expression in the tumoral epithelium was not predictive of the disease-free survival (p = 0.991, log-rank test), even though the follow-up length and the study size were sufficient to detect a significant reduction in disease-free survival among women with stage III-IV compared to stage I-II disease (p<0.001). FSTL3 expression in invasive breast cancer is inversely associated with tumor size and nuclear grade but it does not predict disease relapse in the short term. |
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Prognostic value of follistatin-like 3 in human invasive breast cancerFSTL3FLRGFollistatinActivinBreast cancerCâncer de mamaFollistatin-like 3 (FSTL3) binds and inactivates activin, a growth factor involved with cell growth and differentiation. We have previously shown FSTL3 overexpression in invasive breast cancers, but its clinical relevance remained unexplored. Here we evaluate FSTL3 as a prognostic tool and its relation with clinical and pathological features of breast cancer. A cohort of 154 women diagnosed with invasive breast cancer between 2008 and 2012 was followed up for 5 years. Tumor samples were processed by immunohistochemistry to detect FSTL3 expression in tumor epithelium. FSTL3 expression was classified semiquantitatively and tested for possible correlation with age, menopause status, stage, tumor histological type and grade, estrogen receptor, progesterone receptor, and HER2 expression. Survival plots with Kaplan-Mayer statistics were used to assess whether FSTL3 expression predicted disease-free survival. Our findings show that FSTL3 staining was unrelated to menopausal status, histological type, disease stage, or receptor profile. However, the intensity of FSTL3 immunostaining correlated inversely with tumor size (r = -0.366, p<0.001) and with nuclear grade (p<0.01). The intensity of FSTL3 expression in the tumoral epithelium was not predictive of the disease-free survival (p = 0.991, log-rank test), even though the follow-up length and the study size were sufficient to detect a significant reduction in disease-free survival among women with stage III-IV compared to stage I-II disease (p<0.001). FSTL3 expression in invasive breast cancer is inversely associated with tumor size and nuclear grade but it does not predict disease relapse in the short term.Universidade Federal de Minas GeraisBrasilICB - DEPARTAMENTO DE MORFOLOGIAMED - DEPARTAMENTO DE GINECOLOGIA OBSTETRÍCIAUFMG2023-10-05T23:00:34Z2023-10-05T23:00:34Z2017info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.18632/oncotarget.150261949-2553http://hdl.handle.net/1843/59238https://orcid.org/0000-0002-0873-8160https://orcid.org/0000-0002-8442-8797https://orcid.org/0000-0001-7972-720Xhttps://orcid.org/0000-0003-0275-8686https://orcid.org/0000-0002-8227-7972porOncotargetHenrique CoutoMarcelo BuzelinNivaldo ToppaEnrrico BloiseAlberto WainsteinFernando Marcos Dos Reisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2023-10-05T23:00:34Zoai:repositorio.ufmg.br:1843/59238Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2023-10-05T23:00:34Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
dc.title.none.fl_str_mv |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
title |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
spellingShingle |
Prognostic value of follistatin-like 3 in human invasive breast cancer Henrique Couto FSTL3 FLRG Follistatin Activin Breast cancer Câncer de mama |
title_short |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
title_full |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
title_fullStr |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
title_full_unstemmed |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
title_sort |
Prognostic value of follistatin-like 3 in human invasive breast cancer |
author |
Henrique Couto |
author_facet |
Henrique Couto Marcelo Buzelin Nivaldo Toppa Enrrico Bloise Alberto Wainstein Fernando Marcos Dos Reis |
author_role |
author |
author2 |
Marcelo Buzelin Nivaldo Toppa Enrrico Bloise Alberto Wainstein Fernando Marcos Dos Reis |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Henrique Couto Marcelo Buzelin Nivaldo Toppa Enrrico Bloise Alberto Wainstein Fernando Marcos Dos Reis |
dc.subject.por.fl_str_mv |
FSTL3 FLRG Follistatin Activin Breast cancer Câncer de mama |
topic |
FSTL3 FLRG Follistatin Activin Breast cancer Câncer de mama |
description |
Follistatin-like 3 (FSTL3) binds and inactivates activin, a growth factor involved with cell growth and differentiation. We have previously shown FSTL3 overexpression in invasive breast cancers, but its clinical relevance remained unexplored. Here we evaluate FSTL3 as a prognostic tool and its relation with clinical and pathological features of breast cancer. A cohort of 154 women diagnosed with invasive breast cancer between 2008 and 2012 was followed up for 5 years. Tumor samples were processed by immunohistochemistry to detect FSTL3 expression in tumor epithelium. FSTL3 expression was classified semiquantitatively and tested for possible correlation with age, menopause status, stage, tumor histological type and grade, estrogen receptor, progesterone receptor, and HER2 expression. Survival plots with Kaplan-Mayer statistics were used to assess whether FSTL3 expression predicted disease-free survival. Our findings show that FSTL3 staining was unrelated to menopausal status, histological type, disease stage, or receptor profile. However, the intensity of FSTL3 immunostaining correlated inversely with tumor size (r = -0.366, p<0.001) and with nuclear grade (p<0.01). The intensity of FSTL3 expression in the tumoral epithelium was not predictive of the disease-free survival (p = 0.991, log-rank test), even though the follow-up length and the study size were sufficient to detect a significant reduction in disease-free survival among women with stage III-IV compared to stage I-II disease (p<0.001). FSTL3 expression in invasive breast cancer is inversely associated with tumor size and nuclear grade but it does not predict disease relapse in the short term. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2023-10-05T23:00:34Z 2023-10-05T23:00:34Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.18632/oncotarget.15026 1949-2553 http://hdl.handle.net/1843/59238 https://orcid.org/0000-0002-0873-8160 https://orcid.org/0000-0002-8442-8797 https://orcid.org/0000-0001-7972-720X https://orcid.org/0000-0003-0275-8686 https://orcid.org/0000-0002-8227-7972 |
url |
https://doi.org/10.18632/oncotarget.15026 http://hdl.handle.net/1843/59238 https://orcid.org/0000-0002-0873-8160 https://orcid.org/0000-0002-8442-8797 https://orcid.org/0000-0001-7972-720X https://orcid.org/0000-0003-0275-8686 https://orcid.org/0000-0002-8227-7972 |
identifier_str_mv |
1949-2553 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Oncotarget |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil ICB - DEPARTAMENTO DE MORFOLOGIA MED - DEPARTAMENTO DE GINECOLOGIA OBSTETRÍCIA UFMG |
publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil ICB - DEPARTAMENTO DE MORFOLOGIA MED - DEPARTAMENTO DE GINECOLOGIA OBSTETRÍCIA UFMG |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFMG instname:Universidade Federal de Minas Gerais (UFMG) instacron:UFMG |
instname_str |
Universidade Federal de Minas Gerais (UFMG) |
instacron_str |
UFMG |
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UFMG |
reponame_str |
Repositório Institucional da UFMG |
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Repositório Institucional da UFMG |
repository.name.fl_str_mv |
Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG) |
repository.mail.fl_str_mv |
repositorio@ufmg.br |
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