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State of the art in anti-cancer mAbs

Following Milstein’s discovery, the monoclonal antibodies (mAbs) became a basic tool for biomedical science. In cancer field, since the first mAb was approved by the FDA a great improvement took place making of them a therapeutic option for many cancer types in the current clinical practice. Today,...

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Detalles Bibliográficos
Autores principales: Chiavenna, S. M., Jaworski, J. P., Vendrell, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319201/
https://www.ncbi.nlm.nih.gov/pubmed/28219375
http://dx.doi.org/10.1186/s12929-016-0311-y
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author Chiavenna, S. M.
Jaworski, J. P.
Vendrell, A.
author_facet Chiavenna, S. M.
Jaworski, J. P.
Vendrell, A.
author_sort Chiavenna, S. M.
collection PubMed
description Following Milstein’s discovery, the monoclonal antibodies (mAbs) became a basic tool for biomedical science. In cancer field, since the first mAb was approved by the FDA a great improvement took place making of them a therapeutic option for many cancer types in the current clinical practice. Today, mAbs are being developed to target different molecules with different mechanisms of action and its target potential is unlimited. However, this huge and fast growing new field needs to be organized to better understand the treatment options we have to confront different cancer diseases. Current cancer targeted immunotherapies aim to achieve different goals like the regulation of osteoclast function, the delivery of cytotoxic drugs into tumor cells and the blockade of oncogenic pathways, neo-angiogenesis and immune checkpoints. Here, we reviewed the most relevant therapeutic mAbs for solid tumors available in current clinical practice.
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spelling pubmed-53192012017-02-24 State of the art in anti-cancer mAbs Chiavenna, S. M. Jaworski, J. P. Vendrell, A. J Biomed Sci Review Following Milstein’s discovery, the monoclonal antibodies (mAbs) became a basic tool for biomedical science. In cancer field, since the first mAb was approved by the FDA a great improvement took place making of them a therapeutic option for many cancer types in the current clinical practice. Today, mAbs are being developed to target different molecules with different mechanisms of action and its target potential is unlimited. However, this huge and fast growing new field needs to be organized to better understand the treatment options we have to confront different cancer diseases. Current cancer targeted immunotherapies aim to achieve different goals like the regulation of osteoclast function, the delivery of cytotoxic drugs into tumor cells and the blockade of oncogenic pathways, neo-angiogenesis and immune checkpoints. Here, we reviewed the most relevant therapeutic mAbs for solid tumors available in current clinical practice. BioMed Central 2017-02-20 /pmc/articles/PMC5319201/ /pubmed/28219375 http://dx.doi.org/10.1186/s12929-016-0311-y Text en © The Author(s). 2017 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
Chiavenna, S. M.
Jaworski, J. P.
Vendrell, A.
State of the art in anti-cancer mAbs
title State of the art in anti-cancer mAbs
title_full State of the art in anti-cancer mAbs
title_fullStr State of the art in anti-cancer mAbs
title_full_unstemmed State of the art in anti-cancer mAbs
title_short State of the art in anti-cancer mAbs
title_sort state of the art in anti-cancer mabs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319201/
https://www.ncbi.nlm.nih.gov/pubmed/28219375
http://dx.doi.org/10.1186/s12929-016-0311-y
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