Prognostic value of follistatin-like 3 in human invasive breast cancer

Detalhes bibliográficos
Autor(a) principal: Henrique Couto
Data de Publicação: 2017
Outros Autores: Marcelo Buzelin, Nivaldo Toppa, Enrrico Bloise, Alberto Wainstein, Fernando Marcos Dos Reis
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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spelling 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
institution UFMG
reponame_str Repositório Institucional da UFMG
collection 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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