Pharmaceuticals 2013, 6(2), 124-160; doi:10.3390/ph6020124

siRNA Genome Screening Approaches to Therapeutic Drug Repositioning

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Received: 20 December 2012; in revised form: 10 January 2013 / Accepted: 22 January 2013 / Published: 28 January 2013
(This article belongs to the Special Issue RNAi-Based Therapeutics)
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Abstract: Bridging high-throughput screening (HTS) with RNA interference (RNAi) has allowed for rapid discovery of the molecular basis of many diseases, and identification of potential pathways for developing safe and effective treatments. These features have identified new host gene targets for existing drugs paving the pathway for therapeutic drug repositioning. Using RNAi to discover and help validate new drug targets has also provided a means to filter and prioritize promising therapeutics. This review summarizes these approaches across a spectrum of methods and targets in the host response to pathogens. Particular attention is given to the utility of drug repurposing utilizing the promiscuous nature of some drugs that affect multiple molecules or pathways, and how these biological pathways can be targeted to regulate disease outcome.
Keywords: RNAi; siRNA; miRNA; genome; antiviral; HTS; therapeutic; pathway; virus; bacteria; pathogen; reposition; repurpose; host genes
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.

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MDPI and ACS Style

Perwitasari, O.; Bakre, A.; Tompkins, S.M.; Tripp, R.A. siRNA Genome Screening Approaches to Therapeutic Drug Repositioning. Pharmaceuticals 2013, 6, 124-160.

AMA Style

Perwitasari O, Bakre A, Tompkins SM, Tripp RA. siRNA Genome Screening Approaches to Therapeutic Drug Repositioning. Pharmaceuticals. 2013; 6(2):124-160.

Chicago/Turabian Style

Perwitasari, Olivia; Bakre, Abhijeet; Tompkins, S. M.; Tripp, Ralph A. 2013. "siRNA Genome Screening Approaches to Therapeutic Drug Repositioning." Pharmaceuticals 6, no. 2: 124-160.

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