Cargando…
Antibody Phage Display Libraries: Contributions to Oncology
Since the advent of phage display technology, dating back to 1985, antibody libraries displayed on filamentous phage surfaces have been used to identify specific binders for many different purposes, including the recognition of tumors. Phage display represents a high-throughput technique for screeni...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382779/ https://www.ncbi.nlm.nih.gov/pubmed/22754305 http://dx.doi.org/10.3390/ijms13055420 |
_version_ | 1782236546360934400 |
---|---|
author | Dantas-Barbosa, Carmela de Macedo Brigido, Marcelo Maranhao, Andrea Queiroz |
author_facet | Dantas-Barbosa, Carmela de Macedo Brigido, Marcelo Maranhao, Andrea Queiroz |
author_sort | Dantas-Barbosa, Carmela |
collection | PubMed |
description | Since the advent of phage display technology, dating back to 1985, antibody libraries displayed on filamentous phage surfaces have been used to identify specific binders for many different purposes, including the recognition of tumors. Phage display represents a high-throughput technique for screening billions of random fusion antibodies against virtually any target on the surface or inside cancer cells, or even soluble markers found in patient serum. Many phage display derived binders targeting important tumor markers have been identified. Selection directed to tumoral cells’ surfaces lead to the identification of unknown tumoral markers. Also the improvement of methods that require smaller amounts of cells has opened the possibility to use this approach on patient samples. Robust techniques combining an antibody library displayed on the phage surface and protein microarray allowed the identification of auto antibodies recognized by patient sera. Many Ab molecules directly or indirectly targeting angiogenesis have been identified, and one of them, ramucirumab, has been tested in 27 phase I–III clinical trials in a broad array of cancers. Examples of such antibodies will be discussed here with emphasis on those used as probes for molecular imaging and other clinical trials. |
format | Online Article Text |
id | pubmed-3382779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-33827792012-06-29 Antibody Phage Display Libraries: Contributions to Oncology Dantas-Barbosa, Carmela de Macedo Brigido, Marcelo Maranhao, Andrea Queiroz Int J Mol Sci Review Since the advent of phage display technology, dating back to 1985, antibody libraries displayed on filamentous phage surfaces have been used to identify specific binders for many different purposes, including the recognition of tumors. Phage display represents a high-throughput technique for screening billions of random fusion antibodies against virtually any target on the surface or inside cancer cells, or even soluble markers found in patient serum. Many phage display derived binders targeting important tumor markers have been identified. Selection directed to tumoral cells’ surfaces lead to the identification of unknown tumoral markers. Also the improvement of methods that require smaller amounts of cells has opened the possibility to use this approach on patient samples. Robust techniques combining an antibody library displayed on the phage surface and protein microarray allowed the identification of auto antibodies recognized by patient sera. Many Ab molecules directly or indirectly targeting angiogenesis have been identified, and one of them, ramucirumab, has been tested in 27 phase I–III clinical trials in a broad array of cancers. Examples of such antibodies will be discussed here with emphasis on those used as probes for molecular imaging and other clinical trials. Molecular Diversity Preservation International (MDPI) 2012-05-04 /pmc/articles/PMC3382779/ /pubmed/22754305 http://dx.doi.org/10.3390/ijms13055420 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Dantas-Barbosa, Carmela de Macedo Brigido, Marcelo Maranhao, Andrea Queiroz Antibody Phage Display Libraries: Contributions to Oncology |
title | Antibody Phage Display Libraries: Contributions to Oncology |
title_full | Antibody Phage Display Libraries: Contributions to Oncology |
title_fullStr | Antibody Phage Display Libraries: Contributions to Oncology |
title_full_unstemmed | Antibody Phage Display Libraries: Contributions to Oncology |
title_short | Antibody Phage Display Libraries: Contributions to Oncology |
title_sort | antibody phage display libraries: contributions to oncology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382779/ https://www.ncbi.nlm.nih.gov/pubmed/22754305 http://dx.doi.org/10.3390/ijms13055420 |
work_keys_str_mv | AT dantasbarbosacarmela antibodyphagedisplaylibrariescontributionstooncology AT demacedobrigidomarcelo antibodyphagedisplaylibrariescontributionstooncology AT maranhaoandreaqueiroz antibodyphagedisplaylibrariescontributionstooncology |