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Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers

A better understanding of multimolecular interactions involved in tumor dissemination is required to identify new effective therapies for advanced prostate cancer (PCa). Several groups investigated protein-glycan interactions as critical factors for crosstalk between prostate tumors and their microe...

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Detalles Bibliográficos
Autores principales: Laderach, Diego J., Gentilini, Lucas, Jaworski, Felipe M., Compagno, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800608/
https://www.ncbi.nlm.nih.gov/pubmed/24205440
http://dx.doi.org/10.1155/2013/519436
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author Laderach, Diego J.
Gentilini, Lucas
Jaworski, Felipe M.
Compagno, Daniel
author_facet Laderach, Diego J.
Gentilini, Lucas
Jaworski, Felipe M.
Compagno, Daniel
author_sort Laderach, Diego J.
collection PubMed
description A better understanding of multimolecular interactions involved in tumor dissemination is required to identify new effective therapies for advanced prostate cancer (PCa). Several groups investigated protein-glycan interactions as critical factors for crosstalk between prostate tumors and their microenvironment. This review both discusses whether the “galectin-signature” might serve as a reliable biomarker for the identification of patients with high risk of metastasis and assesses the galectin-glycan lattices as potential novel targets for anticancer therapies. The ultimate goal of this review is to convey how basic findings related to galectins could be in turn translated into clinical settings for patients with advanced PCa.
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spelling pubmed-38006082013-11-07 Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers Laderach, Diego J. Gentilini, Lucas Jaworski, Felipe M. Compagno, Daniel Prostate Cancer Review Article A better understanding of multimolecular interactions involved in tumor dissemination is required to identify new effective therapies for advanced prostate cancer (PCa). Several groups investigated protein-glycan interactions as critical factors for crosstalk between prostate tumors and their microenvironment. This review both discusses whether the “galectin-signature” might serve as a reliable biomarker for the identification of patients with high risk of metastasis and assesses the galectin-glycan lattices as potential novel targets for anticancer therapies. The ultimate goal of this review is to convey how basic findings related to galectins could be in turn translated into clinical settings for patients with advanced PCa. Hindawi Publishing Corporation 2013 2013-09-24 /pmc/articles/PMC3800608/ /pubmed/24205440 http://dx.doi.org/10.1155/2013/519436 Text en Copyright © 2013 Diego J. Laderach et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Laderach, Diego J.
Gentilini, Lucas
Jaworski, Felipe M.
Compagno, Daniel
Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title_full Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title_fullStr Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title_full_unstemmed Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title_short Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate Cancers
title_sort galectins as new prognostic markers and potential therapeutic targets for advanced prostate cancers
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800608/
https://www.ncbi.nlm.nih.gov/pubmed/24205440
http://dx.doi.org/10.1155/2013/519436
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