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Galectin-1 as a potential cancer target

Galectins are a family of structurally related carbohydrate-binding proteins, which are defined by their affinity for poly-N-acetyllactosamine-enriched glycoconjugates and sequence similarities in the carbohydrate recognition domain. Galectin-1, a member of this family, contributes to different even...

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Detalles Bibliográficos
Autor principal: Rabinovich, G A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361964/
https://www.ncbi.nlm.nih.gov/pubmed/15785741
http://dx.doi.org/10.1038/sj.bjc.6602493
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author Rabinovich, G A
author_facet Rabinovich, G A
author_sort Rabinovich, G A
collection PubMed
description Galectins are a family of structurally related carbohydrate-binding proteins, which are defined by their affinity for poly-N-acetyllactosamine-enriched glycoconjugates and sequence similarities in the carbohydrate recognition domain. Galectin-1, a member of this family, contributes to different events associated with cancer biology, including tumour transformation, cell cycle regulation, apoptosis, cell adhesion, migration and inflammation. In addition, recent evidence indicates that galectin-1 contributes to tumour evasion of immune responses. Given the increased interest of tumour biologists and clinical oncologists in this field and the potential use of galectins as novel targets for anticancer drugs, we summarise here recent advances about the role of galectin-1 in different events of tumour growth and metastasis.
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spelling pubmed-23619642009-09-10 Galectin-1 as a potential cancer target Rabinovich, G A Br J Cancer Minireview Galectins are a family of structurally related carbohydrate-binding proteins, which are defined by their affinity for poly-N-acetyllactosamine-enriched glycoconjugates and sequence similarities in the carbohydrate recognition domain. Galectin-1, a member of this family, contributes to different events associated with cancer biology, including tumour transformation, cell cycle regulation, apoptosis, cell adhesion, migration and inflammation. In addition, recent evidence indicates that galectin-1 contributes to tumour evasion of immune responses. Given the increased interest of tumour biologists and clinical oncologists in this field and the potential use of galectins as novel targets for anticancer drugs, we summarise here recent advances about the role of galectin-1 in different events of tumour growth and metastasis. Nature Publishing Group 2005-04-11 2005-03-22 /pmc/articles/PMC2361964/ /pubmed/15785741 http://dx.doi.org/10.1038/sj.bjc.6602493 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Minireview
Rabinovich, G A
Galectin-1 as a potential cancer target
title Galectin-1 as a potential cancer target
title_full Galectin-1 as a potential cancer target
title_fullStr Galectin-1 as a potential cancer target
title_full_unstemmed Galectin-1 as a potential cancer target
title_short Galectin-1 as a potential cancer target
title_sort galectin-1 as a potential cancer target
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361964/
https://www.ncbi.nlm.nih.gov/pubmed/15785741
http://dx.doi.org/10.1038/sj.bjc.6602493
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