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Thrombospondin-1 is a multifaceted player in tumor progression

Thrombospondins are a family of extracellular matrix (ECM) proteins. Thrombospondin-1 (TSP1) was the first member to be identified and is a main player in tumor microenvironment. The diverse functions of TSP1 depend on the interactions between its structural domains and multiple cell surface molecul...

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Detalles Bibliográficos
Autores principales: Huang, Tingting, Sun, Li, Yuan, Xianglin, Qiu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663619/
https://www.ncbi.nlm.nih.gov/pubmed/29137447
http://dx.doi.org/10.18632/oncotarget.19165
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author Huang, Tingting
Sun, Li
Yuan, Xianglin
Qiu, Hong
author_facet Huang, Tingting
Sun, Li
Yuan, Xianglin
Qiu, Hong
author_sort Huang, Tingting
collection PubMed
description Thrombospondins are a family of extracellular matrix (ECM) proteins. Thrombospondin-1 (TSP1) was the first member to be identified and is a main player in tumor microenvironment. The diverse functions of TSP1 depend on the interactions between its structural domains and multiple cell surface molecules. TSP1 acts as an angiogenesis inhibitor by stimulating endothelial cell apoptosis, inhibiting endothelial cell migration and proliferation, and regulating vascular endothelial growth factor bioavailability and activity. In addition to angiogenesis modulation, TSP1 also affects tumor cell adhesion, invasion, migration, proliferation, apoptosis and tumor immunity. This review discusses the multifaceted and sometimes opposite effects of TSP1 on tumor progression depending on the molecular and cellular composition of the microenvironment. Clinical implications of TSP1-related compounds are also discussed.
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spelling pubmed-56636192017-11-13 Thrombospondin-1 is a multifaceted player in tumor progression Huang, Tingting Sun, Li Yuan, Xianglin Qiu, Hong Oncotarget Review Thrombospondins are a family of extracellular matrix (ECM) proteins. Thrombospondin-1 (TSP1) was the first member to be identified and is a main player in tumor microenvironment. The diverse functions of TSP1 depend on the interactions between its structural domains and multiple cell surface molecules. TSP1 acts as an angiogenesis inhibitor by stimulating endothelial cell apoptosis, inhibiting endothelial cell migration and proliferation, and regulating vascular endothelial growth factor bioavailability and activity. In addition to angiogenesis modulation, TSP1 also affects tumor cell adhesion, invasion, migration, proliferation, apoptosis and tumor immunity. This review discusses the multifaceted and sometimes opposite effects of TSP1 on tumor progression depending on the molecular and cellular composition of the microenvironment. Clinical implications of TSP1-related compounds are also discussed. Impact Journals LLC 2017-07-11 /pmc/articles/PMC5663619/ /pubmed/29137447 http://dx.doi.org/10.18632/oncotarget.19165 Text en Copyright: © 2017 Huang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Huang, Tingting
Sun, Li
Yuan, Xianglin
Qiu, Hong
Thrombospondin-1 is a multifaceted player in tumor progression
title Thrombospondin-1 is a multifaceted player in tumor progression
title_full Thrombospondin-1 is a multifaceted player in tumor progression
title_fullStr Thrombospondin-1 is a multifaceted player in tumor progression
title_full_unstemmed Thrombospondin-1 is a multifaceted player in tumor progression
title_short Thrombospondin-1 is a multifaceted player in tumor progression
title_sort thrombospondin-1 is a multifaceted player in tumor progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663619/
https://www.ncbi.nlm.nih.gov/pubmed/29137447
http://dx.doi.org/10.18632/oncotarget.19165
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