Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line
- Autores
- Correa García, S.; Casas, A.; Perotti, C.; Batlle, A.; Bermúdez Moretti, M.
- Año de publicación
- 2003
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK.
Fil:Correa García, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Casas, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Perotti, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Bermúdez Moretti, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. - Fuente
- Br. J. Cancer 2003;89(1):173-177
- Materia
-
δ-aminolevulinic acid
ALA efflux
ALA uptake
Photodynamic therapy
4 aminobutyric acid
aminolevulinic acid
heme derivative
porphobilinogen
porphyrin
succinylacetone
animal cell
article
breast adenocarcinoma
cancer cell culture
cell transport
controlled study
diffusion
heme synthesis
mouse
nonhuman
photodynamic therapy
priority journal
protein function
protein protein interaction
protein transport
temperature dependence
Adenocarcinoma
Aminolevulinic Acid
Animals
gamma-Aminobutyric Acid
Mammary Neoplasms, Animal
Mice
Photochemotherapy
Photosensitizing Agents
Porphyrins
Tumor Cells, Cultured - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/2.5/ar
- Repositorio
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_00070920_v89_n1_p173_CorreaGarcia
Ver los metadatos del registro completo
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Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell lineCorrea García, S.Casas, A.Perotti, C.Batlle, A.Bermúdez Moretti, M.δ-aminolevulinic acidALA effluxALA uptakePhotodynamic therapy4 aminobutyric acidaminolevulinic acidheme derivativeporphobilinogenporphyrinsuccinylacetoneanimal cellarticlebreast adenocarcinomacancer cell culturecell transportcontrolled studydiffusionheme synthesismousenonhumanphotodynamic therapypriority journalprotein functionprotein protein interactionprotein transporttemperature dependenceAdenocarcinomaAminolevulinic AcidAnimalsgamma-Aminobutyric AcidMammary Neoplasms, AnimalMicePhotochemotherapyPhotosensitizing AgentsPorphyrinsTumor Cells, Culturedδ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK.Fil:Correa García, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Casas, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Perotti, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Bermúdez Moretti, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2003info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarciaBr. J. Cancer 2003;89(1):173-177reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-29T13:42:57Zpaperaa:paper_00070920_v89_n1_p173_CorreaGarciaInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-29 13:42:59.041Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse |
dc.title.none.fl_str_mv |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
title |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
spellingShingle |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line Correa García, S. δ-aminolevulinic acid ALA efflux ALA uptake Photodynamic therapy 4 aminobutyric acid aminolevulinic acid heme derivative porphobilinogen porphyrin succinylacetone animal cell article breast adenocarcinoma cancer cell culture cell transport controlled study diffusion heme synthesis mouse nonhuman photodynamic therapy priority journal protein function protein protein interaction protein transport temperature dependence Adenocarcinoma Aminolevulinic Acid Animals gamma-Aminobutyric Acid Mammary Neoplasms, Animal Mice Photochemotherapy Photosensitizing Agents Porphyrins Tumor Cells, Cultured |
title_short |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
title_full |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
title_fullStr |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
title_full_unstemmed |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
title_sort |
Mechanistic studies on δ-aminolevulinic acid uptake and efflux in a mammary adenocarcinoma cell line |
dc.creator.none.fl_str_mv |
Correa García, S. Casas, A. Perotti, C. Batlle, A. Bermúdez Moretti, M. |
author |
Correa García, S. |
author_facet |
Correa García, S. Casas, A. Perotti, C. Batlle, A. Bermúdez Moretti, M. |
author_role |
author |
author2 |
Casas, A. Perotti, C. Batlle, A. Bermúdez Moretti, M. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
δ-aminolevulinic acid ALA efflux ALA uptake Photodynamic therapy 4 aminobutyric acid aminolevulinic acid heme derivative porphobilinogen porphyrin succinylacetone animal cell article breast adenocarcinoma cancer cell culture cell transport controlled study diffusion heme synthesis mouse nonhuman photodynamic therapy priority journal protein function protein protein interaction protein transport temperature dependence Adenocarcinoma Aminolevulinic Acid Animals gamma-Aminobutyric Acid Mammary Neoplasms, Animal Mice Photochemotherapy Photosensitizing Agents Porphyrins Tumor Cells, Cultured |
topic |
δ-aminolevulinic acid ALA efflux ALA uptake Photodynamic therapy 4 aminobutyric acid aminolevulinic acid heme derivative porphobilinogen porphyrin succinylacetone animal cell article breast adenocarcinoma cancer cell culture cell transport controlled study diffusion heme synthesis mouse nonhuman photodynamic therapy priority journal protein function protein protein interaction protein transport temperature dependence Adenocarcinoma Aminolevulinic Acid Animals gamma-Aminobutyric Acid Mammary Neoplasms, Animal Mice Photochemotherapy Photosensitizing Agents Porphyrins Tumor Cells, Cultured |
dc.description.none.fl_txt_mv |
δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK. Fil:Correa García, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Casas, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Perotti, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bermúdez Moretti, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. |
description |
δ-aminolevulinic acid (ALA) is the precursor in the biosynthesis of porphyrins. The knowledge of both the regulation of ALA entrance and efflux from the cells and the control of porphyrin biosynthesis is essential to improve ALA-mediated photodynamic therapy. In this work, we studied the regulation of ALA uptake and efflux by endogenously accumulated ALA and/or porphyrins in murine mammary adenocarcinoma cells. Under our set of conditions, the haem synthesis inhibitor succinyl acetone completely prevented porphobilinogen and porphyrin synthesis from ALA, and led to an increase in the intracellular ALA pool. However, neither intracellular ALA nor porphyrin pools regulate ALA uptake or efflux during the first 15 min of the process. Based on temperature dependence data, ALA but not γ-aminobutyric acid (GABA) efflux is mediated by a diffusion mechanism. Moreover, the addition of extracellular GABA not only did not influence the rate of ALA efflux but on the contrary it affected ALA uptake, showing the contribution of a saturable mechanism for the uptake, but not for the efflux of ALA from the cells. © 2003 Cancer Research UK. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarcia |
url |
http://hdl.handle.net/20.500.12110/paper_00070920_v89_n1_p173_CorreaGarcia |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/2.5/ar |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Br. J. Cancer 2003;89(1):173-177 reponame:Biblioteca Digital (UBA-FCEN) instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales instacron:UBA-FCEN |
reponame_str |
Biblioteca Digital (UBA-FCEN) |
collection |
Biblioteca Digital (UBA-FCEN) |
instname_str |
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
instacron_str |
UBA-FCEN |
institution |
UBA-FCEN |
repository.name.fl_str_mv |
Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
repository.mail.fl_str_mv |
ana@bl.fcen.uba.ar |
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