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RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)

Recombinant TNF-related apoptosis-inducing ligand (TRAIL) is considered a powerful and selective inducer of tumor cell death. We hypothesize that TRAIL’s potential as anticancer agent can be enhanced further by promoting its accumulation in tumor tissue. For this purpose, we developed TRAIL complexe...

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Autores principales: Tarrus, Marc, van der Sloot, Almer M., Temming, Kai, Lacombe, Marie, Opdam, Frank, Quax, Wim J., Molema, Grietje, Poelstra, Klaas, Kok, Robbert J.
Formato: Texto
Lenguaje:English
Publicado: Springer US 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217618/
https://www.ncbi.nlm.nih.gov/pubmed/18071905
http://dx.doi.org/10.1007/s10495-007-0166-5
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author Tarrus, Marc
van der Sloot, Almer M.
Temming, Kai
Lacombe, Marie
Opdam, Frank
Quax, Wim J.
Molema, Grietje
Poelstra, Klaas
Kok, Robbert J.
author_facet Tarrus, Marc
van der Sloot, Almer M.
Temming, Kai
Lacombe, Marie
Opdam, Frank
Quax, Wim J.
Molema, Grietje
Poelstra, Klaas
Kok, Robbert J.
author_sort Tarrus, Marc
collection PubMed
description Recombinant TNF-related apoptosis-inducing ligand (TRAIL) is considered a powerful and selective inducer of tumor cell death. We hypothesize that TRAIL’s potential as anticancer agent can be enhanced further by promoting its accumulation in tumor tissue. For this purpose, we developed TRAIL complexes that bind to angiogenic endothelial cells. We employed an avidin–biotin pretargeting approach, in which biotinylated TRAIL interacted with RGD-equipped avidin. The assembled complexes killed tumor cells (Jurkat T cells) via apoptosis induction. Furthermore, we demonstrated that the association of the RGD-avidin-TRAIL complex onto endothelial cells enhanced the tumor cell killing activity. Endothelial cells were not killed by TRAIL nor its derived complexes. Our approach can facilitate the enrichment of TRAIL onto angiogenic blood vessels, which may enhance intratumoral accumulation. Furthermore, it offers a versatile technology for the complexation of targeting ligands with therapeutic recombinant proteins and by this a novel way to enhance their specificity and activity.
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spelling pubmed-22176182008-01-31 RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL) Tarrus, Marc van der Sloot, Almer M. Temming, Kai Lacombe, Marie Opdam, Frank Quax, Wim J. Molema, Grietje Poelstra, Klaas Kok, Robbert J. Apoptosis Original Paper Recombinant TNF-related apoptosis-inducing ligand (TRAIL) is considered a powerful and selective inducer of tumor cell death. We hypothesize that TRAIL’s potential as anticancer agent can be enhanced further by promoting its accumulation in tumor tissue. For this purpose, we developed TRAIL complexes that bind to angiogenic endothelial cells. We employed an avidin–biotin pretargeting approach, in which biotinylated TRAIL interacted with RGD-equipped avidin. The assembled complexes killed tumor cells (Jurkat T cells) via apoptosis induction. Furthermore, we demonstrated that the association of the RGD-avidin-TRAIL complex onto endothelial cells enhanced the tumor cell killing activity. Endothelial cells were not killed by TRAIL nor its derived complexes. Our approach can facilitate the enrichment of TRAIL onto angiogenic blood vessels, which may enhance intratumoral accumulation. Furthermore, it offers a versatile technology for the complexation of targeting ligands with therapeutic recombinant proteins and by this a novel way to enhance their specificity and activity. Springer US 2007-12-11 2008-02 /pmc/articles/PMC2217618/ /pubmed/18071905 http://dx.doi.org/10.1007/s10495-007-0166-5 Text en © The Author(s) 2007
spellingShingle Original Paper
Tarrus, Marc
van der Sloot, Almer M.
Temming, Kai
Lacombe, Marie
Opdam, Frank
Quax, Wim J.
Molema, Grietje
Poelstra, Klaas
Kok, Robbert J.
RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title_full RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title_fullStr RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title_full_unstemmed RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title_short RGD-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of TNFα related apoptosis inducing ligand (TRAIL)
title_sort rgd-avidin–biotin pretargeting to α(v)β(3) integrin enhances the proapoptotic activity of tnfα related apoptosis inducing ligand (trail)
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217618/
https://www.ncbi.nlm.nih.gov/pubmed/18071905
http://dx.doi.org/10.1007/s10495-007-0166-5
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