The involvement of microRNAs in human pathologies is a firmly established fact. Accordingly, the pharmacological modulation of their activity appears to be a very appealing issue in the development of new types of drugs (miRNA therapeutics). One of the most interesting issues is the possible development of miRNA therapeutics for development of anti-cancer molecules. In this respect appealing molecules are based on peptide nucleic acids (PNAs), displaying a pseudo-peptide backbone composed of N-(2-aminoethyl) glycine units and found to be excellent candidates for antisense and antigene therapies. The major limit in the use of PNAs for alteration of gene expression is the low uptake by eukaryotic cells. The aim of this chapter is to describe methods for determining the activity of PNAs designed to oncomiRNA targets, using as model system miR-221 and its target p27(Kipl) mRNA. The effects of PNAs targeting miR-221 are here presented discussing data obtained using as model system the human breast cancer cell line MDA-MB-231, in which miR-221 is up-regulated and p27(Kipl) down-regulated.
Molecular Methods for Validation of the Biological Activity of Peptide Nucleic Acids Targeting MicroRNAsmiRNA Maturation / Eleonora, Brognara; Enrica, Fabbri; Nicoletta, Bianchi; Alessia, Finotti; Corradini, Roberto; Roberto, Gambari. - 1095:(2014), pp. 165-176. [10.1007/978-1-62703-703-7_14]
Molecular Methods for Validation of the Biological Activity of Peptide Nucleic Acids Targeting MicroRNAsmiRNA Maturation
CORRADINI, Roberto;
2014-01-01
Abstract
The involvement of microRNAs in human pathologies is a firmly established fact. Accordingly, the pharmacological modulation of their activity appears to be a very appealing issue in the development of new types of drugs (miRNA therapeutics). One of the most interesting issues is the possible development of miRNA therapeutics for development of anti-cancer molecules. In this respect appealing molecules are based on peptide nucleic acids (PNAs), displaying a pseudo-peptide backbone composed of N-(2-aminoethyl) glycine units and found to be excellent candidates for antisense and antigene therapies. The major limit in the use of PNAs for alteration of gene expression is the low uptake by eukaryotic cells. The aim of this chapter is to describe methods for determining the activity of PNAs designed to oncomiRNA targets, using as model system miR-221 and its target p27(Kipl) mRNA. The effects of PNAs targeting miR-221 are here presented discussing data obtained using as model system the human breast cancer cell line MDA-MB-231, in which miR-221 is up-regulated and p27(Kipl) down-regulated.File | Dimensione | Formato | |
---|---|---|---|
Micro_RNA_Book_2014_abstract.pdf
non disponibili
Tipologia:
Abstract
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
20.85 kB
Formato
Adobe PDF
|
20.85 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
Micro_RNA_Book_2014_preprint.pdf
non disponibili
Tipologia:
Documento in Pre-print
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
500.65 kB
Formato
Adobe PDF
|
500.65 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.