Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation

Detalhes bibliográficos
Autor(a) principal: Pinto, Sandra
Data de Publicação: 2014
Outros Autores: Martínez-Romero, Alicia, O'Connor, José-Enrique, Gil-Benso, Rosario, San-Miguel, Teresa, Terrádez, Liria, Monteagudo, Carlos, Callaghan, Robert C
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/109367
https://doi.org/10.1186/1471-2407-14-118
Resumo: Background: Chemokines have been implicated in tumor progression and metastasis. In melanoma, chemokine receptors have been implicated in organ selective metastasis by regulating processes such as chemoattraction, adhesion and survival. Methods: In this study we have analyzed, using flow cytometry, the systems formed by the chemokine receptors CXCR3, CXCR4, CXCR7, CCR7 and CCR10 and their ligands in thirteen human melanoma cell lines (five established from primary tumors and eight established from metastasis from different tissues). WM-115 and WM-266.4 melanoma cell lines (obtained from a primary and a metastatic melanoma respectively) were xenografted in nude mice and the tumors and cell lines derived from them were also analyzed. Results: Our results show that the melanoma cell lines do not express or express in a low degree the chemokine receptors on their cell surface. However, melanoma cell lines show intracellular expression of all the aforementioned receptors and most of their respective ligands. When analyzing the xenografts and the cell lines obtained from them we found variations in the intracellular expression of chemokines and chemokine receptors that differed between the primary and metastatic cell lines. However, as well as in the original cell lines, minute or no expression of the chemokine receptors was observed at the cell surface. Conclusions: Coexpression of chemokine receptors and their ligands was found in human melanoma cell lines. However, this expression is intracellular and receptors are not found at the cell membrane nor chemokines are secreted to the cell medium. The levels of expressed chemokine receptors and their ligands show dynamic variations after xenotransplantation that differ depending on the origin of the cell line (from primary tumor or from metastasis).
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spelling Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantationMelanomaCell lineChemokine receptorChemokineXenotransplantationAnimalsCell Line, TumorCell MembraneChemotaxisDisease Models, AnimalHeterograftsHumansImmunohistochemistryIntracellular SpaceMelanomaMiceReceptors, CCRReceptors, CXCRLigandsBackground: Chemokines have been implicated in tumor progression and metastasis. In melanoma, chemokine receptors have been implicated in organ selective metastasis by regulating processes such as chemoattraction, adhesion and survival. Methods: In this study we have analyzed, using flow cytometry, the systems formed by the chemokine receptors CXCR3, CXCR4, CXCR7, CCR7 and CCR10 and their ligands in thirteen human melanoma cell lines (five established from primary tumors and eight established from metastasis from different tissues). WM-115 and WM-266.4 melanoma cell lines (obtained from a primary and a metastatic melanoma respectively) were xenografted in nude mice and the tumors and cell lines derived from them were also analyzed. Results: Our results show that the melanoma cell lines do not express or express in a low degree the chemokine receptors on their cell surface. However, melanoma cell lines show intracellular expression of all the aforementioned receptors and most of their respective ligands. When analyzing the xenografts and the cell lines obtained from them we found variations in the intracellular expression of chemokines and chemokine receptors that differed between the primary and metastatic cell lines. However, as well as in the original cell lines, minute or no expression of the chemokine receptors was observed at the cell surface. Conclusions: Coexpression of chemokine receptors and their ligands was found in human melanoma cell lines. However, this expression is intracellular and receptors are not found at the cell membrane nor chemokines are secreted to the cell medium. The levels of expressed chemokine receptors and their ligands show dynamic variations after xenotransplantation that differ depending on the origin of the cell line (from primary tumor or from metastasis).Springer Nature2014-02-22info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/109367http://hdl.handle.net/10316/109367https://doi.org/10.1186/1471-2407-14-118eng1471-2407Pinto, SandraMartínez-Romero, AliciaO'Connor, José-EnriqueGil-Benso, RosarioSan-Miguel, TeresaTerrádez, LiriaMonteagudo, CarlosCallaghan, Robert Cinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-11T10:00:45Zoai:estudogeral.uc.pt:10316/109367Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:25:34.079789Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
title Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
spellingShingle Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
Pinto, Sandra
Melanoma
Cell line
Chemokine receptor
Chemokine
Xenotransplantation
Animals
Cell Line, Tumor
Cell Membrane
Chemotaxis
Disease Models, Animal
Heterografts
Humans
Immunohistochemistry
Intracellular Space
Melanoma
Mice
Receptors, CCR
Receptors, CXCR
Ligands
title_short Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
title_full Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
title_fullStr Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
title_full_unstemmed Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
title_sort Intracellular coexpression of CXC- and CC- chemokine receptors and their ligands in human melanoma cell lines and dynamic variations after xenotransplantation
author Pinto, Sandra
author_facet Pinto, Sandra
Martínez-Romero, Alicia
O'Connor, José-Enrique
Gil-Benso, Rosario
San-Miguel, Teresa
Terrádez, Liria
Monteagudo, Carlos
Callaghan, Robert C
author_role author
author2 Martínez-Romero, Alicia
O'Connor, José-Enrique
Gil-Benso, Rosario
San-Miguel, Teresa
Terrádez, Liria
Monteagudo, Carlos
Callaghan, Robert C
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pinto, Sandra
Martínez-Romero, Alicia
O'Connor, José-Enrique
Gil-Benso, Rosario
San-Miguel, Teresa
Terrádez, Liria
Monteagudo, Carlos
Callaghan, Robert C
dc.subject.por.fl_str_mv Melanoma
Cell line
Chemokine receptor
Chemokine
Xenotransplantation
Animals
Cell Line, Tumor
Cell Membrane
Chemotaxis
Disease Models, Animal
Heterografts
Humans
Immunohistochemistry
Intracellular Space
Melanoma
Mice
Receptors, CCR
Receptors, CXCR
Ligands
topic Melanoma
Cell line
Chemokine receptor
Chemokine
Xenotransplantation
Animals
Cell Line, Tumor
Cell Membrane
Chemotaxis
Disease Models, Animal
Heterografts
Humans
Immunohistochemistry
Intracellular Space
Melanoma
Mice
Receptors, CCR
Receptors, CXCR
Ligands
description Background: Chemokines have been implicated in tumor progression and metastasis. In melanoma, chemokine receptors have been implicated in organ selective metastasis by regulating processes such as chemoattraction, adhesion and survival. Methods: In this study we have analyzed, using flow cytometry, the systems formed by the chemokine receptors CXCR3, CXCR4, CXCR7, CCR7 and CCR10 and their ligands in thirteen human melanoma cell lines (five established from primary tumors and eight established from metastasis from different tissues). WM-115 and WM-266.4 melanoma cell lines (obtained from a primary and a metastatic melanoma respectively) were xenografted in nude mice and the tumors and cell lines derived from them were also analyzed. Results: Our results show that the melanoma cell lines do not express or express in a low degree the chemokine receptors on their cell surface. However, melanoma cell lines show intracellular expression of all the aforementioned receptors and most of their respective ligands. When analyzing the xenografts and the cell lines obtained from them we found variations in the intracellular expression of chemokines and chemokine receptors that differed between the primary and metastatic cell lines. However, as well as in the original cell lines, minute or no expression of the chemokine receptors was observed at the cell surface. Conclusions: Coexpression of chemokine receptors and their ligands was found in human melanoma cell lines. However, this expression is intracellular and receptors are not found at the cell membrane nor chemokines are secreted to the cell medium. The levels of expressed chemokine receptors and their ligands show dynamic variations after xenotransplantation that differ depending on the origin of the cell line (from primary tumor or from metastasis).
publishDate 2014
dc.date.none.fl_str_mv 2014-02-22
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://hdl.handle.net/10316/109367
http://hdl.handle.net/10316/109367
https://doi.org/10.1186/1471-2407-14-118
url http://hdl.handle.net/10316/109367
https://doi.org/10.1186/1471-2407-14-118
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1471-2407
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Springer Nature
publisher.none.fl_str_mv Springer Nature
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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