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Liu, Jiaqi; Tao, Xianzun; Zhu, Yi; Li, Chong; Ruan, Kai; Diaz-Perez, Zoraida; Rai, Priyamvada; Wang, Hongbo; Zhai, R Grace
eLife, 12/2021, Letnik: 10Journal Article
Gliomas are highly malignant brain tumors with poor prognosis and short survival. NAD has been shown to impact multiple processes that are dysregulated in cancer; however, anti-cancer therapies targeting NAD synthesis have had limited success due to insufficient mechanistic understanding. Here, we adapted a glial neoplasia model and discovered the genetic requirement for NAD synthase nicotinamide mononucleotide adenylyltransferase (NMNAT) in glioma progression in vivo and in human glioma cells. Overexpressing enzymatically active NMNAT significantly promotes glial neoplasia growth and reduces animal viability. Mechanistic analysis suggests that NMNAT interferes with DNA damage-p53-caspase-3 apoptosis signaling pathway by enhancing NAD -dependent posttranslational modifications (PTMs) poly(ADP-ribosyl)ation (PARylation) and deacetylation of p53. Since PARylation and deacetylation reduce p53 pro-apoptotic activity, modulating p53 PTMs could be a key mechanism by which NMNAT promotes glioma growth. Our findings reveal a novel tumorigenic mechanism involving protein complex formation of p53 with NAD synthetic enzyme NMNAT and NAD -dependent PTM enzymes that regulates glioma growth.
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in: SICRIS
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