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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Luginbühl, Vera | - |
dc.contributor.author | Meier, Nicolas | - |
dc.contributor.author | Kovar, Karin | - |
dc.contributor.author | Rohrer, Jack | - |
dc.date.accessioned | 2018-10-09T14:22:32Z | - |
dc.date.available | 2018-10-09T14:22:32Z | - |
dc.date.issued | 2018-05 | - |
dc.identifier.issn | 0734-9750 | de_CH |
dc.identifier.issn | 1873-1899 | de_CH |
dc.identifier.uri | https://digitalcollection.zhaw.ch/handle/11475/11523 | - |
dc.description.abstract | A treasure trove of intracellular cancer drug targets remains hidden behind cell membranes. However, engineered pathogen-derived toxins such as Shiga toxins can deliver small or macromolecular drugs to specific intracellular organelles. After binding to ganglioglobotriaosylceramide (Gb3, CD77), the non-toxic subunit B (StxB) of the Shiga-holotoxin is endocytosed and delivers its payload by a unique retrograde trafficking pathway via the endoplasmic reticulum to the cytosol. This review provides an overview of biomedical applications of StxB-based drug delivery systems in targeted cancer diagnosis and therapy. Biotechnological production of the Stx-material is discussed from the perspective of developing efficacious and safe therapeutics. | de_CH |
dc.language.iso | en | de_CH |
dc.publisher | Elsevier | de_CH |
dc.relation.ispartof | Biotechnology Advances | de_CH |
dc.rights | Licence according to publishing contract | de_CH |
dc.subject | Antibody-drug conjugates | de_CH |
dc.subject | Biotechnological production | de_CH |
dc.subject | Cancer targeting | de_CH |
dc.subject | Intracellular delivery | de_CH |
dc.subject | Receptor-mediated endocytosis | de_CH |
dc.subject | Shiga toxin | de_CH |
dc.subject | Shiga toxin subunit B | de_CH |
dc.subject | Toxin-drug conjugates | de_CH |
dc.subject.ddc | 572: Biochemie | de_CH |
dc.subject.ddc | 610: Medizin und Gesundheit | de_CH |
dc.subject.ddc | 660.6: Biotechnologie | de_CH |
dc.title | Intracellular drug delivery : potential usefulness of engineered Shiga toxin subunit B for targeted cancer therapy | de_CH |
dc.type | Beitrag in wissenschaftlicher Zeitschrift | de_CH |
dcterms.type | Text | de_CH |
zhaw.departement | Life Sciences und Facility Management | de_CH |
zhaw.organisationalunit | Institut für Chemie und Biotechnologie (ICBT) | de_CH |
dc.identifier.doi | 10.1016/j.biotechadv.2018.02.005 | de_CH |
dc.identifier.pmid | 29432805 | de_CH |
zhaw.funding.eu | No | de_CH |
zhaw.issue | 3 | de_CH |
zhaw.originated.zhaw | Yes | de_CH |
zhaw.pages.end | 623 | de_CH |
zhaw.pages.start | 613 | de_CH |
zhaw.publication.status | publishedVersion | de_CH |
zhaw.volume | 36 | de_CH |
zhaw.publication.review | Peer review (Publikation) | de_CH |
Appears in collections: | Publikationen Life Sciences und Facility Management |
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Luginbühl, V., Meier, N., Kovar, K., & Rohrer, J. (2018). Intracellular drug delivery : potential usefulness of engineered Shiga toxin subunit B for targeted cancer therapy. Biotechnology Advances, 36(3), 613–623. https://doi.org/10.1016/j.biotechadv.2018.02.005
Luginbühl, V. et al. (2018) ‘Intracellular drug delivery : potential usefulness of engineered Shiga toxin subunit B for targeted cancer therapy’, Biotechnology Advances, 36(3), pp. 613–623. Available at: https://doi.org/10.1016/j.biotechadv.2018.02.005.
V. Luginbühl, N. Meier, K. Kovar, and J. Rohrer, “Intracellular drug delivery : potential usefulness of engineered Shiga toxin subunit B for targeted cancer therapy,” Biotechnology Advances, vol. 36, no. 3, pp. 613–623, May 2018, doi: 10.1016/j.biotechadv.2018.02.005.
LUGINBÜHL, Vera, Nicolas MEIER, Karin KOVAR und Jack ROHRER, 2018. Intracellular drug delivery : potential usefulness of engineered Shiga toxin subunit B for targeted cancer therapy. Biotechnology Advances. Mai 2018. Bd. 36, Nr. 3, S. 613–623. DOI 10.1016/j.biotechadv.2018.02.005
Luginbühl, Vera, Nicolas Meier, Karin Kovar, and Jack Rohrer. 2018. “Intracellular Drug Delivery : Potential Usefulness of Engineered Shiga Toxin Subunit B for Targeted Cancer Therapy.” Biotechnology Advances 36 (3): 613–23. https://doi.org/10.1016/j.biotechadv.2018.02.005.
Luginbühl, Vera, et al. “Intracellular Drug Delivery : Potential Usefulness of Engineered Shiga Toxin Subunit B for Targeted Cancer Therapy.” Biotechnology Advances, vol. 36, no. 3, May 2018, pp. 613–23, https://doi.org/10.1016/j.biotechadv.2018.02.005.
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