• Takayuki Kurosawa, Shuichi Igarashi, Masatoyo Nishizawa, and Osamu Onodera.
• Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.
• Biochem. Biophys. Res. Commun. 2005 Nov 25; 337 (3): 1012-8.

AbstractFamilial amyloidotic polyneuropathy (FAP) is a hereditary systemic amyloidosis caused by dominantly acting missense mutations in the gene encoding transthyretin (TTR). The most common mutant TTR is of the Val30Met type, which results from a point mutation. Because the major constituent of amyloid fibrils is mutant TTR, agents that selectively suppress mutant TTR expression could be powerful therapeutic tools. This study has been performed to evaluate the use of small interfering RNAs (siRNAs) for the selective silencing of mutant Val30Met TTR in cell culture systems. We have identified an siRNA that specifically inhibits mutant, but not wild-type, TTR expression even in cells expressing both alleles. Thus, this siRNA-based approach may have potential for the gene therapy of FAP.

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