| Literature DB >> 27272383 |
Cédric Chaveroux1, Alain Bruhat1, Valérie Carraro1, Céline Jousse1, Julien Averous1, Anne-Catherine Maurin1, Laurent Parry1, Florent Mesclon1, Yuki Muranishi1, Pierre Cordelier2, Aline Meulle2, Patrick Baril3, Anh Do Thi4, Philippe Ravassard4, Jacques Mallet4,5, Pierre Fafournoux1,3.
Abstract
Widespread application of gene therapy will depend on the development of simple methods to regulate the expression of therapeutic genes. Here we harness an endogenous signaling pathway to regulate therapeutic gene expression through diet. The GCN2-eIF2α signaling pathway is specifically activated by deficiencies in any essential amino acid (EAA); EAA deficiency leads to rapid expression of genes regulated by ATF4-binding cis elements. We found that therapeutic genes under the control of optimized amino acid response elements (AAREs) had low basal expression and high induced expression. We applied our system to regulate the expression of TNFSF10 (TRAIL) in the context of glioma therapy and found that intermittent activation of this gene by EEA-deficient meals retained its therapeutic efficacy while abrogating its toxic effects on normal tissue. The GCN2-eIF2α pathway is expressed in many tissues, including the brain, and is highly specific to EAA deficiency. Our system may be particularly well suited for intermittent regulation of therapeutic transgenes over short or long time periods.Entities:
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Year: 2016 PMID: 27272383 DOI: 10.1038/nbt.3582
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908