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Targeted Delivery of siRNA Therapeutics to Malignant Tumors

Over the past 20 years, a diverse group of ligands targeting surface biomarkers or receptors has been identified with several investigated to target siRNA to tumors. Many approaches to developing tumor-homing peptides, RNA and DNA aptamers, and single-chain variable fragment antibodies by using phag...

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Detalles Bibliográficos
Autores principales: Leng, Qixin, Woodle, Martin C., Mixson, A. James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700508/
https://www.ncbi.nlm.nih.gov/pubmed/29218233
http://dx.doi.org/10.1155/2017/6971297
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author Leng, Qixin
Woodle, Martin C.
Mixson, A. James
author_facet Leng, Qixin
Woodle, Martin C.
Mixson, A. James
author_sort Leng, Qixin
collection PubMed
description Over the past 20 years, a diverse group of ligands targeting surface biomarkers or receptors has been identified with several investigated to target siRNA to tumors. Many approaches to developing tumor-homing peptides, RNA and DNA aptamers, and single-chain variable fragment antibodies by using phage display, in vitro evolution, and recombinant antibody methods could not have been imagined by researchers in the 1980s. Despite these many scientific advances, there is no reason to expect that the ligand field will not continue to evolve. From development of ligands based on novel or existing biomarkers to linking ligands to drugs and gene and antisense delivery systems, several fields have coalesced to facilitate ligand-directed siRNA therapeutics. In this review, we discuss the major categories of ligand-targeted siRNA therapeutics for tumors, as well as the different strategies to identify new ligands.
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spelling pubmed-57005082017-12-07 Targeted Delivery of siRNA Therapeutics to Malignant Tumors Leng, Qixin Woodle, Martin C. Mixson, A. James J Drug Deliv Review Article Over the past 20 years, a diverse group of ligands targeting surface biomarkers or receptors has been identified with several investigated to target siRNA to tumors. Many approaches to developing tumor-homing peptides, RNA and DNA aptamers, and single-chain variable fragment antibodies by using phage display, in vitro evolution, and recombinant antibody methods could not have been imagined by researchers in the 1980s. Despite these many scientific advances, there is no reason to expect that the ligand field will not continue to evolve. From development of ligands based on novel or existing biomarkers to linking ligands to drugs and gene and antisense delivery systems, several fields have coalesced to facilitate ligand-directed siRNA therapeutics. In this review, we discuss the major categories of ligand-targeted siRNA therapeutics for tumors, as well as the different strategies to identify new ligands. Hindawi 2017 2017-11-09 /pmc/articles/PMC5700508/ /pubmed/29218233 http://dx.doi.org/10.1155/2017/6971297 Text en Copyright © 2017 Qixin Leng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Leng, Qixin
Woodle, Martin C.
Mixson, A. James
Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title_full Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title_fullStr Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title_full_unstemmed Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title_short Targeted Delivery of siRNA Therapeutics to Malignant Tumors
title_sort targeted delivery of sirna therapeutics to malignant tumors
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700508/
https://www.ncbi.nlm.nih.gov/pubmed/29218233
http://dx.doi.org/10.1155/2017/6971297
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