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Riboflavin-Targeted Drug Delivery
Active targeting can improve the retention of drugs and drug delivery systems in tumors, thereby enhancing their therapeutic efficacy. In this context, vitamin receptors that are overexpressed in many cancers are promising targets. In the last decade, attention and research were mainly centered on v...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072493/ https://www.ncbi.nlm.nih.gov/pubmed/32012715 http://dx.doi.org/10.3390/cancers12020295 |
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author | Darguzyte, Milita Drude, Natascha Lammers, Twan Kiessling, Fabian |
author_facet | Darguzyte, Milita Drude, Natascha Lammers, Twan Kiessling, Fabian |
author_sort | Darguzyte, Milita |
collection | PubMed |
description | Active targeting can improve the retention of drugs and drug delivery systems in tumors, thereby enhancing their therapeutic efficacy. In this context, vitamin receptors that are overexpressed in many cancers are promising targets. In the last decade, attention and research were mainly centered on vitamin B9 (folate) targeting; however, the focus is slowly shifting towards vitamin B2 (riboflavin). Interestingly, while the riboflavin carrier protein was discovered in the 1960s, the three riboflavin transporters (RFVT 1-3) were only identified recently. It has been shown that riboflavin transporters and the riboflavin carrier protein are overexpressed in many tumor types, tumor stem cells, and the tumor neovasculature. Furthermore, a clinical study has demonstrated that tumor cells exhibit increased riboflavin metabolism as compared to normal cells. Moreover, riboflavin and its derivatives have been conjugated to ultrasmall iron oxide nanoparticles, polyethylene glycol polymers, dendrimers, and liposomes. These conjugates have shown a high affinity towards tumors in preclinical studies. This review article summarizes knowledge on RFVT expression in healthy and pathological tissues, discusses riboflavin internalization pathways, and provides an overview of RF-targeted diagnostics and therapeutics. |
format | Online Article Text |
id | pubmed-7072493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70724932020-03-19 Riboflavin-Targeted Drug Delivery Darguzyte, Milita Drude, Natascha Lammers, Twan Kiessling, Fabian Cancers (Basel) Review Active targeting can improve the retention of drugs and drug delivery systems in tumors, thereby enhancing their therapeutic efficacy. In this context, vitamin receptors that are overexpressed in many cancers are promising targets. In the last decade, attention and research were mainly centered on vitamin B9 (folate) targeting; however, the focus is slowly shifting towards vitamin B2 (riboflavin). Interestingly, while the riboflavin carrier protein was discovered in the 1960s, the three riboflavin transporters (RFVT 1-3) were only identified recently. It has been shown that riboflavin transporters and the riboflavin carrier protein are overexpressed in many tumor types, tumor stem cells, and the tumor neovasculature. Furthermore, a clinical study has demonstrated that tumor cells exhibit increased riboflavin metabolism as compared to normal cells. Moreover, riboflavin and its derivatives have been conjugated to ultrasmall iron oxide nanoparticles, polyethylene glycol polymers, dendrimers, and liposomes. These conjugates have shown a high affinity towards tumors in preclinical studies. This review article summarizes knowledge on RFVT expression in healthy and pathological tissues, discusses riboflavin internalization pathways, and provides an overview of RF-targeted diagnostics and therapeutics. MDPI 2020-01-27 /pmc/articles/PMC7072493/ /pubmed/32012715 http://dx.doi.org/10.3390/cancers12020295 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Darguzyte, Milita Drude, Natascha Lammers, Twan Kiessling, Fabian Riboflavin-Targeted Drug Delivery |
title | Riboflavin-Targeted Drug Delivery |
title_full | Riboflavin-Targeted Drug Delivery |
title_fullStr | Riboflavin-Targeted Drug Delivery |
title_full_unstemmed | Riboflavin-Targeted Drug Delivery |
title_short | Riboflavin-Targeted Drug Delivery |
title_sort | riboflavin-targeted drug delivery |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072493/ https://www.ncbi.nlm.nih.gov/pubmed/32012715 http://dx.doi.org/10.3390/cancers12020295 |
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