Galderisi U, Cipollaro M, Melone M A, Iacomino G, Di Bernardo G, Galano G, Contrufo R, Zappia V, Cascino A
Istituto di Biochimica delle Macromolecole, 2.a Università di Napoli, Facoltà di Medicina, Italy.
Biochem Biophys Res Commun. 1996 Apr 25;221(3):750-4. doi: 10.1006/bbrc.1996.0668.
Antisense phosphorothioate oligonucleotides, targeted against the first codon starting region of DMPK mRNA, were successfully used in K562 and HepG2 cells to decrease DMPK expression. The most effective antisense oligo, MIO1, when added to K562 cells, shows a 75% reduction of the DMPK gene expression 6 hours after addition. The same molecule, when encapsulated in liposomes, delays myotonin mRNA decrease at 24 hours after cell treatment. This considerable success with such inhibition in vitro could be utilised to generate a cell model to study myotonic dystrophy (DM) chemio-physiological alterations.
