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In silico prediction of cancer immunogens: current state of the art

Cancer kills 8 million annually worldwide. Although survival rates in prevalent cancers continue to increase, many cancers have no effective treatment, prompting the search for new and improved protocols. Immunotherapy is a new and exciting addition to the anti-cancer arsenal. The successful and acc...

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Autores principales: Doytchinova, Irini A., Flower, Darren R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856276/
https://www.ncbi.nlm.nih.gov/pubmed/29544447
http://dx.doi.org/10.1186/s12865-018-0248-x
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author Doytchinova, Irini A.
Flower, Darren R.
author_facet Doytchinova, Irini A.
Flower, Darren R.
author_sort Doytchinova, Irini A.
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description Cancer kills 8 million annually worldwide. Although survival rates in prevalent cancers continue to increase, many cancers have no effective treatment, prompting the search for new and improved protocols. Immunotherapy is a new and exciting addition to the anti-cancer arsenal. The successful and accurate identification of aberrant host proteins acting as antigens for vaccination and immunotherapy is a key aspiration for both experimental and computational research. Here we describe key elements of in silico prediction, including databases of cancer antigens and bleeding-edge methodology for their prediction. We also highlight the role dendritic cell vaccines can play and how they can act as delivery mechanisms for epitope ensemble vaccines. Immunoinformatics can help streamline the discovery and utility of Cancer Immunogens.
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spelling pubmed-58562762018-03-22 In silico prediction of cancer immunogens: current state of the art Doytchinova, Irini A. Flower, Darren R. BMC Immunol Review Cancer kills 8 million annually worldwide. Although survival rates in prevalent cancers continue to increase, many cancers have no effective treatment, prompting the search for new and improved protocols. Immunotherapy is a new and exciting addition to the anti-cancer arsenal. The successful and accurate identification of aberrant host proteins acting as antigens for vaccination and immunotherapy is a key aspiration for both experimental and computational research. Here we describe key elements of in silico prediction, including databases of cancer antigens and bleeding-edge methodology for their prediction. We also highlight the role dendritic cell vaccines can play and how they can act as delivery mechanisms for epitope ensemble vaccines. Immunoinformatics can help streamline the discovery and utility of Cancer Immunogens. BioMed Central 2018-03-15 /pmc/articles/PMC5856276/ /pubmed/29544447 http://dx.doi.org/10.1186/s12865-018-0248-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Doytchinova, Irini A.
Flower, Darren R.
In silico prediction of cancer immunogens: current state of the art
title In silico prediction of cancer immunogens: current state of the art
title_full In silico prediction of cancer immunogens: current state of the art
title_fullStr In silico prediction of cancer immunogens: current state of the art
title_full_unstemmed In silico prediction of cancer immunogens: current state of the art
title_short In silico prediction of cancer immunogens: current state of the art
title_sort in silico prediction of cancer immunogens: current state of the art
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856276/
https://www.ncbi.nlm.nih.gov/pubmed/29544447
http://dx.doi.org/10.1186/s12865-018-0248-x
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