RNA aptamers-guided precision cancer medicine
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Version 1 2019-05-20, 10:12Version 1 2019-05-20, 10:12
conference contribution
posted on 2024-06-04, 05:10 authored by Wei DuanWei Duan, T Wang, Sarah ShigdarSarah Shigdar, P Tran© Springer Nature Singapore Pte Ltd. 2018. Aptamers, also known as chemical antibodies, are short single-stranded DNA or RNA that fold into complex three-dimensional structures and bind to target molecules with high affinity and specificity. Aptamers have several advantages that offer the possibility of overcoming limitations of antibodies: they have very low immunogenicity and toxicity; they display high stability at room temperature, in extreme pH, or solvent; once selected, they can be chemically synthesized free from cell-culture-derived contaminants, and they can be manufactured at any time, in large amounts, at relatively low cost and reproducibly; they are smaller and thus can diffuse more rapidly into tissues and organs and they have lower molecular weight that can lead to faster body clearance. To improve cancer treatment outcome, the cancer stem cells must be effectively eliminated. However, with a few exceptions, most anticancer drugs currently on the market are incapable of eliminating cancer stem cells. Although the Nobel Prize-winning RNAi holds great potential as a cancer stem cell therapeutic, its translation into clinical medicine is hampered by the lack of an efficient in vivo delivery system. Based on our recently developed the world first RNA aptamers (chemical antibodies) against cancer stem cell surface marker proteins, we have developed a novel strategy using an all-RNA aptamer-siRNA chimera to target cancer stem cells in vivo. Further optimisation of this platform empowered us, for the first time, to achieve cancer stem cell-targeted delivery of siRNA in mouse xenograft tumour models. This strategy can be applied to cell-targeted silencing of any disease genes in vivo. As our system is amenable to good manufacture processes with scale-up ability, the achievement will accelerate the pace of translating RNAi technology to oncology clinics and help to realise the potential of RNAi in diseases where there are currently no drugs available.
History
Volume
63Pagination
529-535Location
Ho Chi Minh City, VietnamStart date
2016-06-01End date
2016-06-01ISSN
1680-0737ISBN-13
9789811043604Language
engPublication classification
E Conference publication, E1 Full written paper - refereedEditor/Contributor(s)
Van TV, Le TAN, Duc TNTitle of proceedings
BME6 2016 : 6th International Conference on the Development of Biomedical Engineering in VietnamEvent
Development of Biomedical Engineering in Vietnam. Conference (2016 : 6th : Ho Chi Minh City, Vietnam)Publisher
SpringerPlace of publication
Berlin, GermanySeries
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