Targeted Delivery of siRNA Therapeutics to Malignant Tumors
Author(s) -
Qixin Leng,
Martin C. Woodle,
A. James Mixson
Publication year - 2017
Publication title -
journal of drug delivery
Language(s) - English
Resource type - Journals
eISSN - 2090-3014
pISSN - 2090-3022
DOI - 10.1155/2017/6971297
Subject(s) - aptamer , small interfering rna , computational biology , homing (biology) , ligand (biochemistry) , rna , phage display , receptor , rna interference , biology , cancer research , antibody , gene , bioinformatics , medicine , immunology , microbiology and biotechnology , genetics , ecology
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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