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      Aptamer-Based Diagnostics and Therapeutics

      editorial
      1 , 2
      Pharmaceuticals
      MDPI

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          Abstract

          Aptamers were first described almost 30 years ago, with the publication of three separate research papers describing how a randomized library of RNA sequences could be incubated with a target to find a sequence that specifically binds via van der Waals forces, covalent and hydrogen bonding, and not Watson Crick base pairing [1,2,3]. As technology and knowledge have advanced since these initial papers, there have been many developments. These include changes to the selection process, addition of modified bases for better nuclease stability, and the introduction of DNA sequences for aptamers in addition to the first RNA aptamers. Using the simplified high throughput screening of evolving competent binders through iterative cycles of incubation and selection, aptamers have been generated to simple targets such as metal ions, small molecule drugs, and proteins, and more complex targets, such as cells and whole organisms. Aptamers—also known as chemical antibodies—have been investigated for their utility in many applications encompassing diagnostics and therapeutics. They are very similar to monoclonal antibodies and as such, can be used in any application that antibodies have typically been used in. Given the many unique properties of aptamers, they have been also used in novel assays. In this special issue of Pharmaceuticals, we investigate a number of these novel aspects of aptamers and their future in diagnostics and therapeutics. It is unsurprising, given the high burden that cancer places, in terms of non-communicable diseases, that the majority of the articles in this special issue review the potential of aptamers for enhanced diagnostics and therapeutic strategies against cancer. Ciancio et al. review how aptamers can be used with a range of current detection and imaging platforms to improve the sensitivity of cancer detection methods. Through the use of nanoparticles, quantum dots, molecular beacons, fluorescent probes, and microfluidic devices, cancer related biomarkers can be detected in a range of complex solutions at an increased level of sensitivity [4]. Following on from this review of detection methods, Gu et al. present a review of the rolling circle amplification (RCA) method and how it can be used to enhance the limit of detection in medical biosensors and biomedical applications against a multitude of targets [5]. Yoon and Rossi focused their review on all aspects of aptamers in molecular imaging of cancer, ranging from live cell imaging in vitro, to in vivo imaging using fluorescence, magnetic nanoparticles, and radiolabelled aptamers [6]. Camorani et al. focused on one specific subtype of cancer, triple negative breast cancer. This type of breast cancer has a poor prognosis and no current targeted therapeutic, though the authors present compelling evidence for the use of aptamers for the treatment of triple negative breast cancer [7]. Continuing with the cancer theme, while providing some applications for aptamers in the detection of infectious diseases, Molefe et al. discuss the use of aptamers for diagnosis and therapeutic applications against cancer, as well as infectious diseases, with particular focus on viral infectious diseases [8]. It is worth noting that several review articles in this special issue discuss radiolabelling aptamers for targeted molecular imaging. The field of molecular imaging and specifically targeting biomarkers for enhanced detection of lesions and tumours is still relatively new and has developed as technology in the clinic has developed. Hassanzadeh et al. present a review on how to radiolabel aptamers, as well as the different types of chelators for attachment, and the various different forms of radioactive isotypes [9]. These aptamers can then be used for both diagnostics and therapeutics. Adding to this, Khalid et al. discuss various aspects of imaging technology as well as comparing antibodies and peptides to aptamers, in order to demonstrate the utility of aptamers in this emerging area [10]. Soldevilla et al. have brought together work on numerous nucleic acid therapeutics in their review of aptamer-RNAi delivery. One of the many issues that have prevented RNAi entering the clinic has been the non-specific off-target effects. Aptamers can be used as a targeted agent to ensure RNAi gets to the specific sites it is required to reduce these off-target effects [11]. Belleperche and DeRosa present some interesting work on pH-responsive materials, as well as non-canonical nucleic acid base pairing that can shift conformation in response to pH. While this area of aptamer research is still relatively under-researched, there is a lot of untapped potential within this field [12]. An interesting application for aptamers presented by Catuogno et al. is epigenetic regulation. Through the targeting of enzymatic regulators responsible for DNA and chromatin modifications, gene transcriptional regulation can be modulated. Aptamers have the potential to be used as innovative tools to investigate the impact of epigenetic mechanisms on gene expression as well as epigenetic modifiers in numerous diseases, including cancer and neurological disorders [13]. While aptamers have been developed with a multitude of applications, especially for therapeutic applications, as reviewed in this special issue, Bruno offers a note of caution regarding the unmethylated dinucleotide sequence 2′-deoxycytidine-phosphate-2′-guanine (CpG), which has the potential to stimulate the innate immune system. One of Bruno’s recommendations is to perform toxicity testing if CpG motifs cannot be avoided, as well as offering several strategies of limiting their impact [14]. Though it has been nearly 30 years since aptamers were first described, they have been slow to progress into clinical applications. However, within the last few years, we have seen the number of publications with aptamers as a keyword increase, the Aptamer Symposium in Oxford, UK going into its sixth year, the International Society on Aptamers bringing together researchers worldwide, and the Aptamers Journal beginning in 2017. Aptamers are seeing a resurgence and will find their niche in the very near future.

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          Most cited references11

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          Aptamers as Diagnostic Tools in Cancer

          Cancer is the second leading cause of death worldwide. Researchers have been working hard on investigating not only improved therapeutics but also on early detection methods, both critical to increasing treatment efficacy, and developing methods for disease prevention. The use of nucleic acids, or aptamers, has emerged as more specific and accurate cancer diagnostic and therapeutic tools. Aptamers are single-stranded DNA or RNA molecules that recognize specific targets based on unique three-dimensional conformations. Despite the fact aptamer development has been mainly restricted to laboratory settings, the unique attributes of these molecules suggest their high potential for clinical advances in cancer detection. Aptamers can be selected for a wide range of targets, and also linked with an extensive variety of diagnostic agents, via physical or chemical conjugation, to improve previously-established detection methods or to be used as novel biosensors for cancer diagnosis. Consequently, herein we review the principal considerations and recent updates in cancer detection and imaging through aptamer-based molecules.
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            Research Progress on Rolling Circle Amplification (RCA)-Based Biomedical Sensing

            Enhancing the limit of detection (LOD) is significant for crucial diseases. Cancer development could take more than 10 years, from one mutant cell to a visible tumor. Early diagnosis facilitates more effective treatment and leads to higher survival rate for cancer patients. Rolling circle amplification (RCA) is a simple and efficient isothermal enzymatic process that utilizes nuclease to generate long single stranded DNA (ssDNA) or RNA. The functional nucleic acid unit (aptamer, DNAzyme) could be replicated hundreds of times in a short period, and a lower LOD could be achieved if those units are combined with an enzymatic reaction, Surface Plasmon Resonance, electrochemical, or fluorescence detection, and other different kinds of biosensor. Multifarious RCA-based platforms have been developed to detect a variety of targets including DNA, RNA, SNP, proteins, pathogens, cytokines, micromolecules, and diseased cells. In this review, improvements in using the RCA technique for medical biosensors and biomedical applications were summarized and future trends in related research fields described.
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              Aptamer-iRNAs as Therapeutics for Cancer Treatment

              Aptamers are single-stranded oligonucleotides (ssDNA or ssRNA) that bind and recognize their targets with high affinity and specificity due to their complex tertiary structure. Aptamers are selected by a method called SELEX (Systematic Evolution of Ligands by EXponential enrichment). This method has allowed the selection of aptamers to different types of molecules. Since then, many aptamers have been described for the potential treatment of several diseases including cancer. It has been described over the last few years that aptamers represent a very useful tool as therapeutics, especially for cancer therapy. Aptamers, thanks to their intrinsic oligonucleotide nature, present inherent advantages over other molecules, such as cell-based products. Owing to their higher tissue penetrability, safer profile, and targeting capacity, aptamers are likely to become a novel platform for the delivery of many different types of therapeutic cargos. Here we focus the review on interfering RNAs (iRNAs) as aptamer-based targeting delivered agents. We have gathered the most reliable information on aptamers as targeting and carrier agents for the specific delivery of siRNAs, shRNA, microRNAs, and antisense oligonucleotides (ASOs) published in the last few years in the context of cancer therapy.
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                Author and article information

                Journal
                Pharmaceuticals (Basel)
                Pharmaceuticals (Basel)
                pharmaceuticals
                Pharmaceuticals
                MDPI
                1424-8247
                02 January 2019
                March 2019
                : 12
                : 1
                : 6
                Affiliations
                [1 ]School of Medicine Deakin University, Geelong, Victoria 3128, Australia; sarah.shigdar@ 123456deakin.edu.au ; Tel.: +61-03-5227-2846
                [2 ]Centre for Molecular and Medical Research, Deakin University, Geelong, Victoria 3128, Australia
                Article
                pharmaceuticals-12-00006
                10.3390/ph12010006
                6469152
                30609700
                1afbec59-69b7-41a5-a377-ff09b612700f
                © 2019 by the author.

                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/).

                History
                : 26 December 2018
                : 28 December 2018
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