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NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines

Active specific immunotherapy is a promising field in cancer research. N-glycolyl (NGc) gangliosides, and particularly NGcGM3, have received attention as a privileged target for cancer therapy. Many clinical trials have been performed with the anti-NGc-containing gangliosides anti-idiotype monoclona...

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Detalles Bibliográficos
Autores principales: Fernandez, Luis E., Gabri, Mariano R., Guthmann, Marcelo D., Gomez, Roberto E., Gold, Silvia, Fainboim, Leonardo, Gomez, Daniel E., Alonso, Daniel F.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965427/
https://www.ncbi.nlm.nih.gov/pubmed/21048926
http://dx.doi.org/10.1155/2010/814397
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author Fernandez, Luis E.
Gabri, Mariano R.
Guthmann, Marcelo D.
Gomez, Roberto E.
Gold, Silvia
Fainboim, Leonardo
Gomez, Daniel E.
Alonso, Daniel F.
author_facet Fernandez, Luis E.
Gabri, Mariano R.
Guthmann, Marcelo D.
Gomez, Roberto E.
Gold, Silvia
Fainboim, Leonardo
Gomez, Daniel E.
Alonso, Daniel F.
author_sort Fernandez, Luis E.
collection PubMed
description Active specific immunotherapy is a promising field in cancer research. N-glycolyl (NGc) gangliosides, and particularly NGcGM3, have received attention as a privileged target for cancer therapy. Many clinical trials have been performed with the anti-NGc-containing gangliosides anti-idiotype monoclonal antibody racotumomab (formerly known as 1E10) and the conjugated NGcGM3/VSSP vaccine for immunotherapy of melanoma, breast, and lung cancer. The present paper examines the role of NGc-gangliosides in tumor biology as well as the available preclinical and clinical data on these vaccine products. A brief discussion on the relevance of prioritization of cancer antigens in vaccine development is also included.
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spelling pubmed-29654272010-11-03 NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines Fernandez, Luis E. Gabri, Mariano R. Guthmann, Marcelo D. Gomez, Roberto E. Gold, Silvia Fainboim, Leonardo Gomez, Daniel E. Alonso, Daniel F. Clin Dev Immunol Review Article Active specific immunotherapy is a promising field in cancer research. N-glycolyl (NGc) gangliosides, and particularly NGcGM3, have received attention as a privileged target for cancer therapy. Many clinical trials have been performed with the anti-NGc-containing gangliosides anti-idiotype monoclonal antibody racotumomab (formerly known as 1E10) and the conjugated NGcGM3/VSSP vaccine for immunotherapy of melanoma, breast, and lung cancer. The present paper examines the role of NGc-gangliosides in tumor biology as well as the available preclinical and clinical data on these vaccine products. A brief discussion on the relevance of prioritization of cancer antigens in vaccine development is also included. Hindawi Publishing Corporation 2010 2010-10-27 /pmc/articles/PMC2965427/ /pubmed/21048926 http://dx.doi.org/10.1155/2010/814397 Text en Copyright © 2010 Luis E. Fernandez 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
Fernandez, Luis E.
Gabri, Mariano R.
Guthmann, Marcelo D.
Gomez, Roberto E.
Gold, Silvia
Fainboim, Leonardo
Gomez, Daniel E.
Alonso, Daniel F.
NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title_full NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title_fullStr NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title_full_unstemmed NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title_short NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines
title_sort ngcgm3 ganglioside: a privileged target for cancer vaccines
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965427/
https://www.ncbi.nlm.nih.gov/pubmed/21048926
http://dx.doi.org/10.1155/2010/814397
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