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MiR-Synth: a computational resource for the design of multi-site multi-target synthetic miRNAs.


ABSTRACT: RNAi is a powerful tool for the regulation of gene expression. It is widely and successfully employed in functional studies and is now emerging as a promising therapeutic approach. Several RNAi-based clinical trials suggest encouraging results in the treatment of a variety of diseases, including cancer. Here we present miR-Synth, a computational resource for the design of synthetic microRNAs able to target multiple genes in multiple sites. The proposed strategy constitutes a valid alternative to the use of siRNA, allowing the employment of a fewer number of molecules for the inhibition of multiple targets. This may represent a great advantage in designing therapies for diseases caused by crucial cellular pathways altered by multiple dysregulated genes. The system has been successfully validated on two of the most prominent genes associated to lung cancer, c-MET and Epidermal Growth Factor Receptor (EGFR). (See http://microrna.osumc.edu/mir-synth).

SUBMITTER: Lagana A 

PROVIDER: S-EPMC4027198 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

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miR-Synth: a computational resource for the design of multi-site multi-target synthetic miRNAs.

Laganà Alessandro A   Acunzo Mario M   Romano Giulia G   Pulvirenti Alfredo A   Veneziano Dario D   Cascione Luciano L   Giugno Rosalba R   Gasparini Pierluigi P   Shasha Dennis D   Ferro Alfredo A   Croce Carlo Maria CM  

Nucleic acids research 20140313 9


RNAi is a powerful tool for the regulation of gene expression. It is widely and successfully employed in functional studies and is now emerging as a promising therapeutic approach. Several RNAi-based clinical trials suggest encouraging results in the treatment of a variety of diseases, including cancer. Here we present miR-Synth, a computational resource for the design of synthetic microRNAs able to target multiple genes in multiple sites. The proposed strategy constitutes a valid alternative to  ...[more]

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