Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , , , , , , , , |
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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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 |
|
_version_ |
1808129184364494848 |