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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...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer US
2007
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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. |
format | Text |
id | pubmed-2217618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
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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