Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability

Autores
Mascaró, Marilina; Alonso, Exequiel G.; Schweitzer, Karen; Rabassa, Martín Enrique; Carballido, Jessica Andrea; Ibarra, Agustina; Alonso, Eliana N.; Bermúdez, Vicente; Fernández Chavez, Lucía; Coló, Georgina P.; Ferronato, María Julia; Pichel, Pamela; Recio, Sergio; Clemente, Valentina; Fermento, María Eugenia; Facchinetti, María Marta; Curino, Alejandro C.
Año de publicación
2022
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Head and neck squamous cell carcinoma (HNSCC) is a remarkably heterogeneous disease with around 50% mortality, a fact that has prompted researchers to try new approaches to improve patient survival. Hemoxygenase-1 (HO-1) is the rate-limiting step for heme degradation into carbon monoxide, free iron and biliverdin. We have previously reported that HO-1 protein is upregulated in human HNSCC samples and that it is localized in the cytoplasmic and nuclear compartments; additionally, we have demonstrated that HO-1 nuclear localization is associated with malignant progression. In this work, by using pharmacological and genetic experimental approaches, we begin to elucidate the mechanisms through which HO-1 plays a role in HNSCC. We found that high HO-1 mRNA was associated with decreased patient survival in early stages of HNSCC. In vitro experiments have shown that full-length HO-1 localizes in the cytoplasm, and that, depending on its enzymatic activity, it increases cell viability and promotes cell cycle progression. Instead, HO-1 does not alter migration capacity. Furthermore, we show that C-terminal truncated HO-1 localizes into the nucleus, increases cell viability and promotes cell cycle progression. In conclusion, we herein demonstrate that HO-1 displays protumor activities in HNSCC that depend, at least in part, on the nuclear localization of HO-1.
Centro de Investigaciones Inmunológicas Básicas y Aplicadas
Materia
Medicina
Biología
hemoxygenase-1
nucleus
cancer
head and neck
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/155707

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network_name_str SEDICI (UNLP)
spelling Hemoxygenase-1 Promotes Head and Neck Cancer Cell ViabilityMascaró, MarilinaAlonso, Exequiel G.Schweitzer, KarenRabassa, Martín EnriqueCarballido, Jessica AndreaIbarra, AgustinaAlonso, Eliana N.Bermúdez, VicenteFernández Chavez, LucíaColó, Georgina P.Ferronato, María JuliaPichel, PamelaRecio, SergioClemente, ValentinaFermento, María EugeniaFacchinetti, María MartaCurino, Alejandro C.MedicinaBiologíahemoxygenase-1nucleuscancerhead and neckHead and neck squamous cell carcinoma (HNSCC) is a remarkably heterogeneous disease with around 50% mortality, a fact that has prompted researchers to try new approaches to improve patient survival. Hemoxygenase-1 (HO-1) is the rate-limiting step for heme degradation into carbon monoxide, free iron and biliverdin. We have previously reported that HO-1 protein is upregulated in human HNSCC samples and that it is localized in the cytoplasmic and nuclear compartments; additionally, we have demonstrated that HO-1 nuclear localization is associated with malignant progression. In this work, by using pharmacological and genetic experimental approaches, we begin to elucidate the mechanisms through which HO-1 plays a role in HNSCC. We found that high HO-1 mRNA was associated with decreased patient survival in early stages of HNSCC. In vitro experiments have shown that full-length HO-1 localizes in the cytoplasm, and that, depending on its enzymatic activity, it increases cell viability and promotes cell cycle progression. Instead, HO-1 does not alter migration capacity. Furthermore, we show that C-terminal truncated HO-1 localizes into the nucleus, increases cell viability and promotes cell cycle progression. In conclusion, we herein demonstrate that HO-1 displays protumor activities in HNSCC that depend, at least in part, on the nuclear localization of HO-1.Centro de Investigaciones Inmunológicas Básicas y Aplicadas2022-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/155707enginfo:eu-repo/semantics/altIdentifier/issn/2076-3921info:eu-repo/semantics/altIdentifier/doi/10.3390/antiox11102077info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:40:26Zoai:sedici.unlp.edu.ar:10915/155707Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:40:26.913SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
title Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
spellingShingle Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
Mascaró, Marilina
Medicina
Biología
hemoxygenase-1
nucleus
cancer
head and neck
title_short Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
title_full Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
title_fullStr Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
title_full_unstemmed Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
title_sort Hemoxygenase-1 Promotes Head and Neck Cancer Cell Viability
dc.creator.none.fl_str_mv Mascaró, Marilina
Alonso, Exequiel G.
Schweitzer, Karen
Rabassa, Martín Enrique
Carballido, Jessica Andrea
Ibarra, Agustina
Alonso, Eliana N.
Bermúdez, Vicente
Fernández Chavez, Lucía
Coló, Georgina P.
Ferronato, María Julia
Pichel, Pamela
Recio, Sergio
Clemente, Valentina
Fermento, María Eugenia
Facchinetti, María Marta
Curino, Alejandro C.
author Mascaró, Marilina
author_facet Mascaró, Marilina
Alonso, Exequiel G.
Schweitzer, Karen
Rabassa, Martín Enrique
Carballido, Jessica Andrea
Ibarra, Agustina
Alonso, Eliana N.
Bermúdez, Vicente
Fernández Chavez, Lucía
Coló, Georgina P.
Ferronato, María Julia
Pichel, Pamela
Recio, Sergio
Clemente, Valentina
Fermento, María Eugenia
Facchinetti, María Marta
Curino, Alejandro C.
author_role author
author2 Alonso, Exequiel G.
Schweitzer, Karen
Rabassa, Martín Enrique
Carballido, Jessica Andrea
Ibarra, Agustina
Alonso, Eliana N.
Bermúdez, Vicente
Fernández Chavez, Lucía
Coló, Georgina P.
Ferronato, María Julia
Pichel, Pamela
Recio, Sergio
Clemente, Valentina
Fermento, María Eugenia
Facchinetti, María Marta
Curino, Alejandro C.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Medicina
Biología
hemoxygenase-1
nucleus
cancer
head and neck
topic Medicina
Biología
hemoxygenase-1
nucleus
cancer
head and neck
dc.description.none.fl_txt_mv Head and neck squamous cell carcinoma (HNSCC) is a remarkably heterogeneous disease with around 50% mortality, a fact that has prompted researchers to try new approaches to improve patient survival. Hemoxygenase-1 (HO-1) is the rate-limiting step for heme degradation into carbon monoxide, free iron and biliverdin. We have previously reported that HO-1 protein is upregulated in human HNSCC samples and that it is localized in the cytoplasmic and nuclear compartments; additionally, we have demonstrated that HO-1 nuclear localization is associated with malignant progression. In this work, by using pharmacological and genetic experimental approaches, we begin to elucidate the mechanisms through which HO-1 plays a role in HNSCC. We found that high HO-1 mRNA was associated with decreased patient survival in early stages of HNSCC. In vitro experiments have shown that full-length HO-1 localizes in the cytoplasm, and that, depending on its enzymatic activity, it increases cell viability and promotes cell cycle progression. Instead, HO-1 does not alter migration capacity. Furthermore, we show that C-terminal truncated HO-1 localizes into the nucleus, increases cell viability and promotes cell cycle progression. In conclusion, we herein demonstrate that HO-1 displays protumor activities in HNSCC that depend, at least in part, on the nuclear localization of HO-1.
Centro de Investigaciones Inmunológicas Básicas y Aplicadas
description Head and neck squamous cell carcinoma (HNSCC) is a remarkably heterogeneous disease with around 50% mortality, a fact that has prompted researchers to try new approaches to improve patient survival. Hemoxygenase-1 (HO-1) is the rate-limiting step for heme degradation into carbon monoxide, free iron and biliverdin. We have previously reported that HO-1 protein is upregulated in human HNSCC samples and that it is localized in the cytoplasmic and nuclear compartments; additionally, we have demonstrated that HO-1 nuclear localization is associated with malignant progression. In this work, by using pharmacological and genetic experimental approaches, we begin to elucidate the mechanisms through which HO-1 plays a role in HNSCC. We found that high HO-1 mRNA was associated with decreased patient survival in early stages of HNSCC. In vitro experiments have shown that full-length HO-1 localizes in the cytoplasm, and that, depending on its enzymatic activity, it increases cell viability and promotes cell cycle progression. Instead, HO-1 does not alter migration capacity. Furthermore, we show that C-terminal truncated HO-1 localizes into the nucleus, increases cell viability and promotes cell cycle progression. In conclusion, we herein demonstrate that HO-1 displays protumor activities in HNSCC that depend, at least in part, on the nuclear localization of HO-1.
publishDate 2022
dc.date.none.fl_str_mv 2022-10
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/155707
url http://sedici.unlp.edu.ar/handle/10915/155707
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/2076-3921
info:eu-repo/semantics/altIdentifier/doi/10.3390/antiox11102077
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
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dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
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