Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer

Detalhes bibliográficos
Autor(a) principal: Calmon, Marilia Freitas
Data de Publicação: 2015
Outros Autores: Jeschke, Jana, Zhang, Wei, Dhir, Mashaal, Siebenkäs, Cornelia, Herrera, Alexander, Tsai, Hsing-Chen, O’Hagan, Heather M., Pappou, Emmanouil P., Hooker, Craig M., Fu, Tao, Schuebel, Kornel E., Gabrielson, Edward, Rahal, Paula, Herman, James G., Baylin, Stephen B., Ahuja, Nita
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1080/15592294.2015.1050173
http://hdl.handle.net/11449/220467
Resumo: Neurofilament heavy polypeptide (NEFH) has recently been identified as a candidate DNA hypermethylated gene within the functional breast cancer hypermethylome. NEFH exists in a complex with neurofilament medium polypeptide (NEFM) and neurofilament light polypeptide (NEFL) to form neurofilaments, which are structural components of the cytoskeleton in mature neurons. Recent studies reported the deregulation of these proteins in several malignancies, suggesting that neurofilaments may have a role in other cell types as well. Using a comprehensive approach, we studied the epigenetic inactivation of neurofilament genes in breast cancer and the functional significance of this event. We report that DNA methylation-associated silencing of NEFH, NEFL, and NEFM in breast cancer is frequent, cancer-specific, and correlates with clinical features of disease progression. DNA methylation-mediated inactivation of these genes occurs also in multiple other cancer histologies including pancreas, gastric, and colon. Restoration of NEFH function, the major subunit of the neurofilament complex, reduces proliferation and growth of breast cancer cells and arrests them in Go/G1 phase of the cell cycle along with a reduction in migration and invasion. These findings suggest that DNA methylation-mediated silencing of the neurofilament genes NEFH, NEFM, and NEFL are frequent events that may contribute to the progression of breast cancer and possibly other malignancies.
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spelling Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancerBreast cancerDNA methylationNEFHNEFLNEFMTCGANeurofilament heavy polypeptide (NEFH) has recently been identified as a candidate DNA hypermethylated gene within the functional breast cancer hypermethylome. NEFH exists in a complex with neurofilament medium polypeptide (NEFM) and neurofilament light polypeptide (NEFL) to form neurofilaments, which are structural components of the cytoskeleton in mature neurons. Recent studies reported the deregulation of these proteins in several malignancies, suggesting that neurofilaments may have a role in other cell types as well. Using a comprehensive approach, we studied the epigenetic inactivation of neurofilament genes in breast cancer and the functional significance of this event. We report that DNA methylation-associated silencing of NEFH, NEFL, and NEFM in breast cancer is frequent, cancer-specific, and correlates with clinical features of disease progression. DNA methylation-mediated inactivation of these genes occurs also in multiple other cancer histologies including pancreas, gastric, and colon. Restoration of NEFH function, the major subunit of the neurofilament complex, reduces proliferation and growth of breast cancer cells and arrests them in Go/G1 phase of the cell cycle along with a reduction in migration and invasion. These findings suggest that DNA methylation-mediated silencing of the neurofilament genes NEFH, NEFM, and NEFL are frequent events that may contribute to the progression of breast cancer and possibly other malignancies.National Institutes of HealthDepartment of Biology University of São Paulo StateDepartment of Surgery Johns Hopkins UniversityDepartment of Oncology Johns Hopkins UniversityLaboratory of Cancer Epigenetics Université Libre de BruxellesDepartment of Pathology Johns Hopkins UniversityDepartment of Urology Johns Hopkins UniversityUniversidade de São Paulo (USP)Johns Hopkins UniversityUniversité Libre de BruxellesCalmon, Marilia FreitasJeschke, JanaZhang, WeiDhir, MashaalSiebenkäs, CorneliaHerrera, AlexanderTsai, Hsing-ChenO’Hagan, Heather M.Pappou, Emmanouil P.Hooker, Craig M.Fu, TaoSchuebel, Kornel E.Gabrielson, EdwardRahal, PaulaHerman, James G.Baylin, Stephen B.Ahuja, Nita2022-04-28T19:01:38Z2022-04-28T19:01:38Z2015-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article622-632http://dx.doi.org/10.1080/15592294.2015.1050173Epigenetics, v. 10, n. 7, p. 622-632, 2015.1559-23081559-2294http://hdl.handle.net/11449/22046710.1080/15592294.2015.10501732-s2.0-84943739682Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengEpigeneticsinfo:eu-repo/semantics/openAccess2022-04-28T19:01:38Zoai:repositorio.unesp.br:11449/220467Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:17:10.865007Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
title Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
spellingShingle Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
Calmon, Marilia Freitas
Breast cancer
DNA methylation
NEFH
NEFL
NEFM
TCGA
title_short Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
title_full Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
title_fullStr Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
title_full_unstemmed Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
title_sort Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
author Calmon, Marilia Freitas
author_facet Calmon, Marilia Freitas
Jeschke, Jana
Zhang, Wei
Dhir, Mashaal
Siebenkäs, Cornelia
Herrera, Alexander
Tsai, Hsing-Chen
O’Hagan, Heather M.
Pappou, Emmanouil P.
Hooker, Craig M.
Fu, Tao
Schuebel, Kornel E.
Gabrielson, Edward
Rahal, Paula
Herman, James G.
Baylin, Stephen B.
Ahuja, Nita
author_role author
author2 Jeschke, Jana
Zhang, Wei
Dhir, Mashaal
Siebenkäs, Cornelia
Herrera, Alexander
Tsai, Hsing-Chen
O’Hagan, Heather M.
Pappou, Emmanouil P.
Hooker, Craig M.
Fu, Tao
Schuebel, Kornel E.
Gabrielson, Edward
Rahal, Paula
Herman, James G.
Baylin, Stephen B.
Ahuja, Nita
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Johns Hopkins University
Université Libre de Bruxelles
dc.contributor.author.fl_str_mv Calmon, Marilia Freitas
Jeschke, Jana
Zhang, Wei
Dhir, Mashaal
Siebenkäs, Cornelia
Herrera, Alexander
Tsai, Hsing-Chen
O’Hagan, Heather M.
Pappou, Emmanouil P.
Hooker, Craig M.
Fu, Tao
Schuebel, Kornel E.
Gabrielson, Edward
Rahal, Paula
Herman, James G.
Baylin, Stephen B.
Ahuja, Nita
dc.subject.por.fl_str_mv Breast cancer
DNA methylation
NEFH
NEFL
NEFM
TCGA
topic Breast cancer
DNA methylation
NEFH
NEFL
NEFM
TCGA
description Neurofilament heavy polypeptide (NEFH) has recently been identified as a candidate DNA hypermethylated gene within the functional breast cancer hypermethylome. NEFH exists in a complex with neurofilament medium polypeptide (NEFM) and neurofilament light polypeptide (NEFL) to form neurofilaments, which are structural components of the cytoskeleton in mature neurons. Recent studies reported the deregulation of these proteins in several malignancies, suggesting that neurofilaments may have a role in other cell types as well. Using a comprehensive approach, we studied the epigenetic inactivation of neurofilament genes in breast cancer and the functional significance of this event. We report that DNA methylation-associated silencing of NEFH, NEFL, and NEFM in breast cancer is frequent, cancer-specific, and correlates with clinical features of disease progression. DNA methylation-mediated inactivation of these genes occurs also in multiple other cancer histologies including pancreas, gastric, and colon. Restoration of NEFH function, the major subunit of the neurofilament complex, reduces proliferation and growth of breast cancer cells and arrests them in Go/G1 phase of the cell cycle along with a reduction in migration and invasion. These findings suggest that DNA methylation-mediated silencing of the neurofilament genes NEFH, NEFM, and NEFL are frequent events that may contribute to the progression of breast cancer and possibly other malignancies.
publishDate 2015
dc.date.none.fl_str_mv 2015-01-01
2022-04-28T19:01:38Z
2022-04-28T19:01:38Z
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/10.1080/15592294.2015.1050173
Epigenetics, v. 10, n. 7, p. 622-632, 2015.
1559-2308
1559-2294
http://hdl.handle.net/11449/220467
10.1080/15592294.2015.1050173
2-s2.0-84943739682
url http://dx.doi.org/10.1080/15592294.2015.1050173
http://hdl.handle.net/11449/220467
identifier_str_mv Epigenetics, v. 10, n. 7, p. 622-632, 2015.
1559-2308
1559-2294
10.1080/15592294.2015.1050173
2-s2.0-84943739682
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Epigenetics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 622-632
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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