Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps

Detalhes bibliográficos
Autor(a) principal: Abrão, Féres
Data de Publicação: 2018
Outros Autores: Modotti, Waldir Pereira [UNESP], Spadoto-Dias, Daniel [UNESP], Bueloni-Dias, Flávia Neves [UNESP], Leite, Nilton José [UNESP], Peres, Gustavo Filipov [UNESP], Elias, Leonardo Vieira [UNESP], Custódio Domingues, Maria Aparecida [UNESP], Dias, Rogério [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1097/MD.0000000000012304
http://hdl.handle.net/11449/188159
Resumo: The aim of this retrospective cross-sectional study was to assess the usefulness of phosphase and tensin homolog deleted on chromosome 10 (PTEN) and p53 protein immunoexpression in predicting the risk of malignancy in endometrial polyps. The study was conducted at tertiary public hospital, university teaching center, and private practice clinic. A total of 159 patients with endometrial polyps who underwent hysteroscopic polypectomy between January 2010 to December 2014 were included. p53 and PTEN immunoexpression were assessed in histologic endometrial polyp samples. Patients were allocated into 2 groups: group A, endometrial polyps without atypia (120), and group B, endometrial polyps with atypia (39), which were subdivided into A1 (80) and B1 (21) = p53-/PTEN+ immunostaining; A2 (20) and B2 (11) = p53+/PTEN+; A3 (14) and B3 (4) = p53+/PTEN-; A4 (6) and B4 (3) = p53-/PTEN-. There was no significant difference between groups regarding clinical and epidemiologic parameters, except for age. Neoplasia incidence within groups was higher when at least 1 marker was abnormally stained (in group A, P=.0089, odds ratio [OR]=13.94 [1.62; 120.27]; in group B, P=.0255, OR 12.73 [1.38; 117.27]). Overall neoplasia incidence was higher in group B than in group A (20.5% vs 5.8%; P=.0113). Malignant neoplasia was found more frequently in patients with p53+ (P=.0006, OR=7.67 [2.30; 25.54]) and PTEN- (P=.0043; OR=5.43 [1.77; 16.61]). Immunohistochemical analysis using p53 and PTEN as markers, either alone or concomitantly, can be useful to predict malignant transformation in cases of endometrial polyps.
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spelling Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polypsHysteroscopyImmunohistochemistryPolypsPTEN phosphohydrolaseTumor suppressor p53 proteinThe aim of this retrospective cross-sectional study was to assess the usefulness of phosphase and tensin homolog deleted on chromosome 10 (PTEN) and p53 protein immunoexpression in predicting the risk of malignancy in endometrial polyps. The study was conducted at tertiary public hospital, university teaching center, and private practice clinic. A total of 159 patients with endometrial polyps who underwent hysteroscopic polypectomy between January 2010 to December 2014 were included. p53 and PTEN immunoexpression were assessed in histologic endometrial polyp samples. Patients were allocated into 2 groups: group A, endometrial polyps without atypia (120), and group B, endometrial polyps with atypia (39), which were subdivided into A1 (80) and B1 (21) = p53-/PTEN+ immunostaining; A2 (20) and B2 (11) = p53+/PTEN+; A3 (14) and B3 (4) = p53+/PTEN-; A4 (6) and B4 (3) = p53-/PTEN-. There was no significant difference between groups regarding clinical and epidemiologic parameters, except for age. Neoplasia incidence within groups was higher when at least 1 marker was abnormally stained (in group A, P=.0089, odds ratio [OR]=13.94 [1.62; 120.27]; in group B, P=.0255, OR 12.73 [1.38; 117.27]). Overall neoplasia incidence was higher in group B than in group A (20.5% vs 5.8%; P=.0113). Malignant neoplasia was found more frequently in patients with p53+ (P=.0006, OR=7.67 [2.30; 25.54]) and PTEN- (P=.0043; OR=5.43 [1.77; 16.61]). Immunohistochemical analysis using p53 and PTEN as markers, either alone or concomitantly, can be useful to predict malignant transformation in cases of endometrial polyps.Department of Gynecology and Obstetrics of Hospital Beneficente Unimar - HBU University of Marília UNIMAR Medical SchoolMedical Assistance Institute - IAMDepartment of Gynecology and Obstetrics Botucatu Medical School São Paulo State University/UNESPDepartment of Pathological Anatomy Botucatu Medical School São Paulo State University/UNESPDepartment of Gynecology and Obstetrics Botucatu Medical School São Paulo State University/UNESPDepartment of Pathological Anatomy Botucatu Medical School São Paulo State University/UNESPUNIMAR Medical SchoolMedical Assistance Institute - IAMUniversidade Estadual Paulista (Unesp)Abrão, FéresModotti, Waldir Pereira [UNESP]Spadoto-Dias, Daniel [UNESP]Bueloni-Dias, Flávia Neves [UNESP]Leite, Nilton José [UNESP]Peres, Gustavo Filipov [UNESP]Elias, Leonardo Vieira [UNESP]Custódio Domingues, Maria Aparecida [UNESP]Dias, Rogério [UNESP]2019-10-06T15:59:12Z2019-10-06T15:59:12Z2018-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1097/MD.0000000000012304Medicine (United States), v. 97, n. 38, 2018.1536-59640025-7974http://hdl.handle.net/11449/18815910.1097/MD.00000000000123042-s2.0-85054443591Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMedicine (United States)info:eu-repo/semantics/openAccess2024-09-03T13:14:43Zoai:repositorio.unesp.br:11449/188159Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:14:43Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
title Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
spellingShingle Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
Abrão, Féres
Hysteroscopy
Immunohistochemistry
Polyps
PTEN phosphohydrolase
Tumor suppressor p53 protein
title_short Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
title_full Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
title_fullStr Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
title_full_unstemmed Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
title_sort Concomitant p53 and PTEN immunoexpression to predict the risk of malignancy in endometrial polyps
author Abrão, Féres
author_facet Abrão, Féres
Modotti, Waldir Pereira [UNESP]
Spadoto-Dias, Daniel [UNESP]
Bueloni-Dias, Flávia Neves [UNESP]
Leite, Nilton José [UNESP]
Peres, Gustavo Filipov [UNESP]
Elias, Leonardo Vieira [UNESP]
Custódio Domingues, Maria Aparecida [UNESP]
Dias, Rogério [UNESP]
author_role author
author2 Modotti, Waldir Pereira [UNESP]
Spadoto-Dias, Daniel [UNESP]
Bueloni-Dias, Flávia Neves [UNESP]
Leite, Nilton José [UNESP]
Peres, Gustavo Filipov [UNESP]
Elias, Leonardo Vieira [UNESP]
Custódio Domingues, Maria Aparecida [UNESP]
Dias, Rogério [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv UNIMAR Medical School
Medical Assistance Institute - IAM
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Abrão, Féres
Modotti, Waldir Pereira [UNESP]
Spadoto-Dias, Daniel [UNESP]
Bueloni-Dias, Flávia Neves [UNESP]
Leite, Nilton José [UNESP]
Peres, Gustavo Filipov [UNESP]
Elias, Leonardo Vieira [UNESP]
Custódio Domingues, Maria Aparecida [UNESP]
Dias, Rogério [UNESP]
dc.subject.por.fl_str_mv Hysteroscopy
Immunohistochemistry
Polyps
PTEN phosphohydrolase
Tumor suppressor p53 protein
topic Hysteroscopy
Immunohistochemistry
Polyps
PTEN phosphohydrolase
Tumor suppressor p53 protein
description The aim of this retrospective cross-sectional study was to assess the usefulness of phosphase and tensin homolog deleted on chromosome 10 (PTEN) and p53 protein immunoexpression in predicting the risk of malignancy in endometrial polyps. The study was conducted at tertiary public hospital, university teaching center, and private practice clinic. A total of 159 patients with endometrial polyps who underwent hysteroscopic polypectomy between January 2010 to December 2014 were included. p53 and PTEN immunoexpression were assessed in histologic endometrial polyp samples. Patients were allocated into 2 groups: group A, endometrial polyps without atypia (120), and group B, endometrial polyps with atypia (39), which were subdivided into A1 (80) and B1 (21) = p53-/PTEN+ immunostaining; A2 (20) and B2 (11) = p53+/PTEN+; A3 (14) and B3 (4) = p53+/PTEN-; A4 (6) and B4 (3) = p53-/PTEN-. There was no significant difference between groups regarding clinical and epidemiologic parameters, except for age. Neoplasia incidence within groups was higher when at least 1 marker was abnormally stained (in group A, P=.0089, odds ratio [OR]=13.94 [1.62; 120.27]; in group B, P=.0255, OR 12.73 [1.38; 117.27]). Overall neoplasia incidence was higher in group B than in group A (20.5% vs 5.8%; P=.0113). Malignant neoplasia was found more frequently in patients with p53+ (P=.0006, OR=7.67 [2.30; 25.54]) and PTEN- (P=.0043; OR=5.43 [1.77; 16.61]). Immunohistochemical analysis using p53 and PTEN as markers, either alone or concomitantly, can be useful to predict malignant transformation in cases of endometrial polyps.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-01
2019-10-06T15:59:12Z
2019-10-06T15:59:12Z
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 http://dx.doi.org/10.1097/MD.0000000000012304
Medicine (United States), v. 97, n. 38, 2018.
1536-5964
0025-7974
http://hdl.handle.net/11449/188159
10.1097/MD.0000000000012304
2-s2.0-85054443591
url http://dx.doi.org/10.1097/MD.0000000000012304
http://hdl.handle.net/11449/188159
identifier_str_mv Medicine (United States), v. 97, n. 38, 2018.
1536-5964
0025-7974
10.1097/MD.0000000000012304
2-s2.0-85054443591
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Medicine (United States)
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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