Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas

Detalhes bibliográficos
Autor(a) principal: Brunhara, Bruno B.
Data de Publicação: 2021
Outros Autores: Becker, Aline P., Neder, Luciano, Gonçalves, Paola G. [UNESP], de Oliveira, Cristiane [UNESP], Clara, Carlos A., Reis, Rui M., Bidinotto, Lucas T. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1111/neup.12698
http://hdl.handle.net/11449/206887
Resumo: Pilocytic astrocytoma (PA) is the most frequent solid neoplasm in childhood. It has a good 5-year overall survival (90% in childhood and 52% in adults). However, up to 20% of patients experience residual tumor growth, recurrence, and death. Although the main genetic alteration of PAs, including KIAA1549:BRAF fusion, involves chromosome 7q34, we previously found frequent loss in chr9q34.3 locus in a small subset of these tumors. Among the genes present in this locus, EGFL7 is related to poor prognosis in several tumor types. In this study, we aimed to assess EGFL7 expression through immunohistochemistry, and to evaluate its prognostic value in a series of 64 clinically and molecularly well-characterized pilocytic astrocytomas. We found high expression of EGFL7 in 71.9% of patients. Low EGFL7 expression was associated with older patients, the mean age mainly older than 11 years (P = 0.027). EGFL7 expression was not associated with presence of KIAA1549:BRAF fusion, BRAF mutation, FGFR1 mutation, nor FGFR1 duplication. Moreover, high EGFL7 expression was associated with high FGFR1 (P = 0.037) and 5′-deoxy-5′-methyltioadenosine phosphorylase (MTAP) (P = 0.005) expression, and with unfavorable outcome of patients (P = 0.047). Multivariate analysis revealed low EGFL7 expression related to older patients and high EGFL7 expression related to retained expression of MTAP. In addition, we found a borderline significance of unfavorable outcome and high EGFL7 expression. Finally, EGFL7 expression was not associated with overall or event-free survival of PA patients. Our findings point to EGFL7 expression as a novel candidate prognostic marker in PA, which should be further investigated.
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spelling Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomasEGFL7FGFR1immunohistochemistryMTAPpilocytic astrocytomaPilocytic astrocytoma (PA) is the most frequent solid neoplasm in childhood. It has a good 5-year overall survival (90% in childhood and 52% in adults). However, up to 20% of patients experience residual tumor growth, recurrence, and death. Although the main genetic alteration of PAs, including KIAA1549:BRAF fusion, involves chromosome 7q34, we previously found frequent loss in chr9q34.3 locus in a small subset of these tumors. Among the genes present in this locus, EGFL7 is related to poor prognosis in several tumor types. In this study, we aimed to assess EGFL7 expression through immunohistochemistry, and to evaluate its prognostic value in a series of 64 clinically and molecularly well-characterized pilocytic astrocytomas. We found high expression of EGFL7 in 71.9% of patients. Low EGFL7 expression was associated with older patients, the mean age mainly older than 11 years (P = 0.027). EGFL7 expression was not associated with presence of KIAA1549:BRAF fusion, BRAF mutation, FGFR1 mutation, nor FGFR1 duplication. Moreover, high EGFL7 expression was associated with high FGFR1 (P = 0.037) and 5′-deoxy-5′-methyltioadenosine phosphorylase (MTAP) (P = 0.005) expression, and with unfavorable outcome of patients (P = 0.047). Multivariate analysis revealed low EGFL7 expression related to older patients and high EGFL7 expression related to retained expression of MTAP. In addition, we found a borderline significance of unfavorable outcome and high EGFL7 expression. Finally, EGFL7 expression was not associated with overall or event-free survival of PA patients. Our findings point to EGFL7 expression as a novel candidate prognostic marker in PA, which should be further investigated.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Molecular Oncology Research Center Barretos Cancer HospitalBarretos School of Health Sciences Dr. Paulo Prata – FACISBDepartment of Radiation Oncology The Ohio State UniversityDepartment of Pathology Botucatu Medical School São Paulo State University-UNESPDepartment of Neurosurgery Barretos Cancer HospitalLife and Health Sciences Research Institute (ICVS) School of Medicine University of MinhoICVS/3B's – PT Government Associate LaboratoryDepartment of Pathology Botucatu Medical School São Paulo State University-UNESPFAPESP: 2012/19590-0FAPESP: 2016/21727-4FAPESP: 2016/23919-8FAPESP: 2017/09749-5CNPq: 472447/2013-0Barretos Cancer HospitalDr. Paulo Prata – FACISBThe Ohio State UniversityUniversidade Estadual Paulista (Unesp)University of MinhoICVS/3B's – PT Government Associate LaboratoryBrunhara, Bruno B.Becker, Aline P.Neder, LucianoGonçalves, Paola G. [UNESP]de Oliveira, Cristiane [UNESP]Clara, Carlos A.Reis, Rui M.Bidinotto, Lucas T. [UNESP]2021-06-25T10:45:30Z2021-06-25T10:45:30Z2021-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article21-28http://dx.doi.org/10.1111/neup.12698Neuropathology, v. 41, n. 1, p. 21-28, 2021.1440-17890919-6544http://hdl.handle.net/11449/20688710.1111/neup.126982-s2.0-85096770608Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengNeuropathologyinfo:eu-repo/semantics/openAccess2021-10-23T15:33:58Zoai:repositorio.unesp.br:11449/206887Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T15:33:58Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
title Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
spellingShingle Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
Brunhara, Bruno B.
EGFL7
FGFR1
immunohistochemistry
MTAP
pilocytic astrocytoma
title_short Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
title_full Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
title_fullStr Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
title_full_unstemmed Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
title_sort Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas
author Brunhara, Bruno B.
author_facet Brunhara, Bruno B.
Becker, Aline P.
Neder, Luciano
Gonçalves, Paola G. [UNESP]
de Oliveira, Cristiane [UNESP]
Clara, Carlos A.
Reis, Rui M.
Bidinotto, Lucas T. [UNESP]
author_role author
author2 Becker, Aline P.
Neder, Luciano
Gonçalves, Paola G. [UNESP]
de Oliveira, Cristiane [UNESP]
Clara, Carlos A.
Reis, Rui M.
Bidinotto, Lucas T. [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Barretos Cancer Hospital
Dr. Paulo Prata – FACISB
The Ohio State University
Universidade Estadual Paulista (Unesp)
University of Minho
ICVS/3B's – PT Government Associate Laboratory
dc.contributor.author.fl_str_mv Brunhara, Bruno B.
Becker, Aline P.
Neder, Luciano
Gonçalves, Paola G. [UNESP]
de Oliveira, Cristiane [UNESP]
Clara, Carlos A.
Reis, Rui M.
Bidinotto, Lucas T. [UNESP]
dc.subject.por.fl_str_mv EGFL7
FGFR1
immunohistochemistry
MTAP
pilocytic astrocytoma
topic EGFL7
FGFR1
immunohistochemistry
MTAP
pilocytic astrocytoma
description Pilocytic astrocytoma (PA) is the most frequent solid neoplasm in childhood. It has a good 5-year overall survival (90% in childhood and 52% in adults). However, up to 20% of patients experience residual tumor growth, recurrence, and death. Although the main genetic alteration of PAs, including KIAA1549:BRAF fusion, involves chromosome 7q34, we previously found frequent loss in chr9q34.3 locus in a small subset of these tumors. Among the genes present in this locus, EGFL7 is related to poor prognosis in several tumor types. In this study, we aimed to assess EGFL7 expression through immunohistochemistry, and to evaluate its prognostic value in a series of 64 clinically and molecularly well-characterized pilocytic astrocytomas. We found high expression of EGFL7 in 71.9% of patients. Low EGFL7 expression was associated with older patients, the mean age mainly older than 11 years (P = 0.027). EGFL7 expression was not associated with presence of KIAA1549:BRAF fusion, BRAF mutation, FGFR1 mutation, nor FGFR1 duplication. Moreover, high EGFL7 expression was associated with high FGFR1 (P = 0.037) and 5′-deoxy-5′-methyltioadenosine phosphorylase (MTAP) (P = 0.005) expression, and with unfavorable outcome of patients (P = 0.047). Multivariate analysis revealed low EGFL7 expression related to older patients and high EGFL7 expression related to retained expression of MTAP. In addition, we found a borderline significance of unfavorable outcome and high EGFL7 expression. Finally, EGFL7 expression was not associated with overall or event-free survival of PA patients. Our findings point to EGFL7 expression as a novel candidate prognostic marker in PA, which should be further investigated.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:45:30Z
2021-06-25T10:45:30Z
2021-02-01
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/10.1111/neup.12698
Neuropathology, v. 41, n. 1, p. 21-28, 2021.
1440-1789
0919-6544
http://hdl.handle.net/11449/206887
10.1111/neup.12698
2-s2.0-85096770608
url http://dx.doi.org/10.1111/neup.12698
http://hdl.handle.net/11449/206887
identifier_str_mv Neuropathology, v. 41, n. 1, p. 21-28, 2021.
1440-1789
0919-6544
10.1111/neup.12698
2-s2.0-85096770608
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Neuropathology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 21-28
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
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