Role of the extracellular matrix in variations of invasive pathways in lung cancers
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/109719 https://doi.org/10.1590/1414-431x20122263 |
Resumo: | Among the most common features of highly invasive tumors, such as lung adenocarcinomas (AD) and squamous cell carcinomas (SqCC), is the massive degradation of the extracellular matrix. The remarkable qualitative and quantitative modifications of hyaluronidases (HAases), hyaluronan synthases (HAS), E-cadherin adhesion molecules, and the transforming growth factor β (TGF-β) may favor invasion, cellular motility, and proliferation. We examined HAase proteins (Hyal), HAS, E-cadherin, and TGF-β profiles in lung AD subtypes and SqCC obtained from smokers and non-smokers. Fifty-six patients, median age 64 years, who underwent lobectomy for AD (N = 31) and SqCC (N = 25) were included in the study. HAS-1, -2 and -3, and Hyal-1 and -3 were significantly more expressed by tumor cells than normal and stroma cells (P < 0.01). When stratified according to histologic types, HAS-3 and Hyal-1 immunoreactivity was significantly increased in tumor cells of AD (P = 0.01) and stroma of SqCC (P = 0.002), respectively. Tobacco history in patients with AD was significantly associated with increased HAS-3 immunoreactivity in tumor cells (P < 0.01). Stroma cells of SqCC from non-smokers presented a significant association with HAS-3 (P < 0.01). Hyal, HAS, E-cadherin, and TGF-β modulate a different tumor-induced invasive pathway in lung AD subgroups and SqCC. HAases in resected AD and SqCC were strongly related to the prognosis. Therefore, our findings suggest that strategies aimed at preventing high HAS-3 and Hyal-1 synthesis, or local responses to low TGF-β and E-cadherin, may have a greater impact in lung cancer prognosis. |
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Role of the extracellular matrix in variations of invasive pathways in lung cancersLung cancerE-cadherinTGF-bHAS-1, HAS-2 and HAS-3Hyal-1 and Hyal-3ImmunohistochemistryPrognosis and morphometryAdenocarcinomaAdenocarcinoma of LungAdultAgedAged, 80 and overCadherinsCarcinoma, Squamous CellCell Adhesion MoleculesExtracellular MatrixFemaleGlucuronosyltransferaseHumansHyaluronan SynthasesLung NeoplasmsMaleMiddle AgedNeoplasm InvasivenessNeoplasm StagingAmong the most common features of highly invasive tumors, such as lung adenocarcinomas (AD) and squamous cell carcinomas (SqCC), is the massive degradation of the extracellular matrix. The remarkable qualitative and quantitative modifications of hyaluronidases (HAases), hyaluronan synthases (HAS), E-cadherin adhesion molecules, and the transforming growth factor β (TGF-β) may favor invasion, cellular motility, and proliferation. We examined HAase proteins (Hyal), HAS, E-cadherin, and TGF-β profiles in lung AD subtypes and SqCC obtained from smokers and non-smokers. Fifty-six patients, median age 64 years, who underwent lobectomy for AD (N = 31) and SqCC (N = 25) were included in the study. HAS-1, -2 and -3, and Hyal-1 and -3 were significantly more expressed by tumor cells than normal and stroma cells (P < 0.01). When stratified according to histologic types, HAS-3 and Hyal-1 immunoreactivity was significantly increased in tumor cells of AD (P = 0.01) and stroma of SqCC (P = 0.002), respectively. Tobacco history in patients with AD was significantly associated with increased HAS-3 immunoreactivity in tumor cells (P < 0.01). Stroma cells of SqCC from non-smokers presented a significant association with HAS-3 (P < 0.01). Hyal, HAS, E-cadherin, and TGF-β modulate a different tumor-induced invasive pathway in lung AD subgroups and SqCC. HAases in resected AD and SqCC were strongly related to the prognosis. Therefore, our findings suggest that strategies aimed at preventing high HAS-3 and Hyal-1 synthesis, or local responses to low TGF-β and E-cadherin, may have a greater impact in lung cancer prognosis.Associacao Brasileira de Divulgacao Cientifica2013-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/109719http://hdl.handle.net/10316/109719https://doi.org/10.1590/1414-431x20122263engde Sá, V. K.Carvalho, L.Gomes, A.Alarcão, A.Silva, M. R.Couceiro, P.Sousa, V.Soares, F. A.Capelozzi, V. L.info: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:RCAAP2023-10-24T09:49:38Zoai:estudogeral.uc.pt:10316/109719Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:25:52.358955Repositório 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 |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
title |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
spellingShingle |
Role of the extracellular matrix in variations of invasive pathways in lung cancers de Sá, V. K. Lung cancer E-cadherin TGF-b HAS-1, HAS-2 and HAS-3 Hyal-1 and Hyal-3 Immunohistochemistry Prognosis and morphometry Adenocarcinoma Adenocarcinoma of Lung Adult Aged Aged, 80 and over Cadherins Carcinoma, Squamous Cell Cell Adhesion Molecules Extracellular Matrix Female Glucuronosyltransferase Humans Hyaluronan Synthases Lung Neoplasms Male Middle Aged Neoplasm Invasiveness Neoplasm Staging |
title_short |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
title_full |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
title_fullStr |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
title_full_unstemmed |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
title_sort |
Role of the extracellular matrix in variations of invasive pathways in lung cancers |
author |
de Sá, V. K. |
author_facet |
de Sá, V. K. Carvalho, L. Gomes, A. Alarcão, A. Silva, M. R. Couceiro, P. Sousa, V. Soares, F. A. Capelozzi, V. L. |
author_role |
author |
author2 |
Carvalho, L. Gomes, A. Alarcão, A. Silva, M. R. Couceiro, P. Sousa, V. Soares, F. A. Capelozzi, V. L. |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
de Sá, V. K. Carvalho, L. Gomes, A. Alarcão, A. Silva, M. R. Couceiro, P. Sousa, V. Soares, F. A. Capelozzi, V. L. |
dc.subject.por.fl_str_mv |
Lung cancer E-cadherin TGF-b HAS-1, HAS-2 and HAS-3 Hyal-1 and Hyal-3 Immunohistochemistry Prognosis and morphometry Adenocarcinoma Adenocarcinoma of Lung Adult Aged Aged, 80 and over Cadherins Carcinoma, Squamous Cell Cell Adhesion Molecules Extracellular Matrix Female Glucuronosyltransferase Humans Hyaluronan Synthases Lung Neoplasms Male Middle Aged Neoplasm Invasiveness Neoplasm Staging |
topic |
Lung cancer E-cadherin TGF-b HAS-1, HAS-2 and HAS-3 Hyal-1 and Hyal-3 Immunohistochemistry Prognosis and morphometry Adenocarcinoma Adenocarcinoma of Lung Adult Aged Aged, 80 and over Cadherins Carcinoma, Squamous Cell Cell Adhesion Molecules Extracellular Matrix Female Glucuronosyltransferase Humans Hyaluronan Synthases Lung Neoplasms Male Middle Aged Neoplasm Invasiveness Neoplasm Staging |
description |
Among the most common features of highly invasive tumors, such as lung adenocarcinomas (AD) and squamous cell carcinomas (SqCC), is the massive degradation of the extracellular matrix. The remarkable qualitative and quantitative modifications of hyaluronidases (HAases), hyaluronan synthases (HAS), E-cadherin adhesion molecules, and the transforming growth factor β (TGF-β) may favor invasion, cellular motility, and proliferation. We examined HAase proteins (Hyal), HAS, E-cadherin, and TGF-β profiles in lung AD subtypes and SqCC obtained from smokers and non-smokers. Fifty-six patients, median age 64 years, who underwent lobectomy for AD (N = 31) and SqCC (N = 25) were included in the study. HAS-1, -2 and -3, and Hyal-1 and -3 were significantly more expressed by tumor cells than normal and stroma cells (P < 0.01). When stratified according to histologic types, HAS-3 and Hyal-1 immunoreactivity was significantly increased in tumor cells of AD (P = 0.01) and stroma of SqCC (P = 0.002), respectively. Tobacco history in patients with AD was significantly associated with increased HAS-3 immunoreactivity in tumor cells (P < 0.01). Stroma cells of SqCC from non-smokers presented a significant association with HAS-3 (P < 0.01). Hyal, HAS, E-cadherin, and TGF-β modulate a different tumor-induced invasive pathway in lung AD subgroups and SqCC. HAases in resected AD and SqCC were strongly related to the prognosis. Therefore, our findings suggest that strategies aimed at preventing high HAS-3 and Hyal-1 synthesis, or local responses to low TGF-β and E-cadherin, may have a greater impact in lung cancer prognosis. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01 |
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/10316/109719 http://hdl.handle.net/10316/109719 https://doi.org/10.1590/1414-431x20122263 |
url |
http://hdl.handle.net/10316/109719 https://doi.org/10.1590/1414-431x20122263 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Associacao Brasileira de Divulgacao Cientifica |
publisher.none.fl_str_mv |
Associacao Brasileira de Divulgacao Cientifica |
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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799134140269854720 |