As previously mentioned, examples of longevity resulting from disruption of the GH/IGF-1 and/or insulin signaling pathway are mainly derived from early life manipulations 6,17,18 , whereas brief exposure to GH (and IGF-1) treatment early in development is sufficient to partially abrogate the exceptional longevity of Ames Dwarf mice 20
Specifically, FOXO4-DRI peptide has been researched as a decoy that may compete with FOXO4 for p53 binding, so it may disrupt the FOXO4p53 interaction in laboratory systems
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