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Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2

Vascular endothelial growth factor (VEGF)-A blockade has been validated clinically as a treatment for human cancers. Angiopoietin-2 (Ang-2) is a key regulator of blood vessel remodeling and maturation. In tumors, Ang-2 is up-regulated and an unfavorable prognostic factor. Recent data demonstrated th...

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Autores principales: Scheuer, Werner, Thomas, Markus, Hanke, Petra, Sam, Johannes, Osl, Franz, Weininger, Diana, Baehner, Monika, Seeber, Stefan, Kettenberger, Hubert, Schanzer, Jürgen, Brinkmann, Ulrich, Weidner, K. Michael, Regula, Jörg, Klein, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966847/
https://www.ncbi.nlm.nih.gov/pubmed/26864324
http://dx.doi.org/10.1080/19420862.2016.1147640
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author Scheuer, Werner
Thomas, Markus
Hanke, Petra
Sam, Johannes
Osl, Franz
Weininger, Diana
Baehner, Monika
Seeber, Stefan
Kettenberger, Hubert
Schanzer, Jürgen
Brinkmann, Ulrich
Weidner, K. Michael
Regula, Jörg
Klein, Christian
author_facet Scheuer, Werner
Thomas, Markus
Hanke, Petra
Sam, Johannes
Osl, Franz
Weininger, Diana
Baehner, Monika
Seeber, Stefan
Kettenberger, Hubert
Schanzer, Jürgen
Brinkmann, Ulrich
Weidner, K. Michael
Regula, Jörg
Klein, Christian
author_sort Scheuer, Werner
collection PubMed
description Vascular endothelial growth factor (VEGF)-A blockade has been validated clinically as a treatment for human cancers. Angiopoietin-2 (Ang-2) is a key regulator of blood vessel remodeling and maturation. In tumors, Ang-2 is up-regulated and an unfavorable prognostic factor. Recent data demonstrated that Ang-2 inhibition mediates anti-tumoral effects. We generated a tetravalent bispecific antibody (Ang-2-VEGF-TAvi6) targeting VEGF-A with 2 arms based on bevacizumab (Avastin®), and targeting Ang-2 with 2 arms based on a novel anti-Ang-2 antibody (LC06). The two Ang-2-targeting single-chain variable fragments are disulfide-stabilized and fused to the C-terminus of the heavy chain of bevacizumab. Treatment with Ang-2-VEGF-A-TAvi6 led to a complete abrogation of angiogenesis in the cornea micropocket assay. Metastatic spread and tumor growth of subcutaneous, orthotopic and anti-VEGF-A resistant tumors were also efficiently inhibited. These data further establish Ang-2-VEGF bispecific antibodies as a promising anti-angiogenic, anti-metastatic and anti-tumor agent for the treatment of cancer.
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spelling pubmed-49668472016-08-23 Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2 Scheuer, Werner Thomas, Markus Hanke, Petra Sam, Johannes Osl, Franz Weininger, Diana Baehner, Monika Seeber, Stefan Kettenberger, Hubert Schanzer, Jürgen Brinkmann, Ulrich Weidner, K. Michael Regula, Jörg Klein, Christian MAbs Reports Vascular endothelial growth factor (VEGF)-A blockade has been validated clinically as a treatment for human cancers. Angiopoietin-2 (Ang-2) is a key regulator of blood vessel remodeling and maturation. In tumors, Ang-2 is up-regulated and an unfavorable prognostic factor. Recent data demonstrated that Ang-2 inhibition mediates anti-tumoral effects. We generated a tetravalent bispecific antibody (Ang-2-VEGF-TAvi6) targeting VEGF-A with 2 arms based on bevacizumab (Avastin®), and targeting Ang-2 with 2 arms based on a novel anti-Ang-2 antibody (LC06). The two Ang-2-targeting single-chain variable fragments are disulfide-stabilized and fused to the C-terminus of the heavy chain of bevacizumab. Treatment with Ang-2-VEGF-A-TAvi6 led to a complete abrogation of angiogenesis in the cornea micropocket assay. Metastatic spread and tumor growth of subcutaneous, orthotopic and anti-VEGF-A resistant tumors were also efficiently inhibited. These data further establish Ang-2-VEGF bispecific antibodies as a promising anti-angiogenic, anti-metastatic and anti-tumor agent for the treatment of cancer. Taylor & Francis 2016-02-10 /pmc/articles/PMC4966847/ /pubmed/26864324 http://dx.doi.org/10.1080/19420862.2016.1147640 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Reports
Scheuer, Werner
Thomas, Markus
Hanke, Petra
Sam, Johannes
Osl, Franz
Weininger, Diana
Baehner, Monika
Seeber, Stefan
Kettenberger, Hubert
Schanzer, Jürgen
Brinkmann, Ulrich
Weidner, K. Michael
Regula, Jörg
Klein, Christian
Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title_full Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title_fullStr Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title_full_unstemmed Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title_short Anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (TAvi6) targeting VEGF-A and angiopoietin-2
title_sort anti-tumoral, anti-angiogenic and anti-metastatic efficacy of a tetravalent bispecific antibody (tavi6) targeting vegf-a and angiopoietin-2
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966847/
https://www.ncbi.nlm.nih.gov/pubmed/26864324
http://dx.doi.org/10.1080/19420862.2016.1147640
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