p63 promotes cell survival through fatty acid synthase

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p63 promotes cell survival through fatty acid synthase

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Title: p63 promotes cell survival through fatty acid synthase
Author: Di Napoli, Arianna; Seeley, Apryle; Amato, Angela M.; O'Regan, Esther; Sabbisetti, Venkata S; Ghebremichael, Musie Syum; Loda, Massimo; Signoretti, Sabina

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Citation: Sabbisetti, Venkata, Arianna Di Napoli, Apryle Seeley, Angela M. Amato, Esther O'Regan, Musie Ghebremichael, Massimo Loda, and Sabina Signoretti. 2009. p63 promotes cell survival through fatty acid synthase. PLoS ONE 4(6): e5877.
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Abstract: There is increasing evidence that p63, and specifically ΔNp63, plays a central role in both development and tumorigenesis by promoting epithelial cell survival. However, few studies have addressed the molecular mechanisms through which such important function is exerted. Fatty acid synthase (FASN), a key enzyme that synthesizes long-chain fatty acids and is involved in both embryogenesis and cancer, has been recently proposed as a direct target of p53 family members, including p63 and p73. Here we show that knockdown of either total or ΔN-specific p63 isoforms in squamous cell carcinoma (SCC9) or immortalized prostate epithelial (iPrEC) cells caused a decrease in cell viability by inducing apoptosis without affecting the cell cycle. p63 silencing significantly reduced both the expression and the activity of FASN. Importantly, stable overexpression of either FASN or myristoylated AKT (myr-AKT) was able to partially rescue cells from cell death induced by p63 silencing. FASN induced AKT phosphorylation and a significant reduction in cell viability was observed when FASN-overexpressing SCC9 cells were treated with an AKT inhibitor after p63 knockdown, indicating that AKT plays a major role in FASN-mediated survival. Activated AKT did not cause any alteration in the FASN protein levels but induced its activity, suggesting that the rescue from apoptosis documented in the p63-silenced cells expressing myr-AKT cells may be partially mediated by FASN. Finally, we demonstrated that p63 and FASN expression are positively associated in clinical squamous cell carcinoma samples as well as in the developing prostate. Taken together, our findings demonstrate that FASN is a functionally relevant target of p63 and is required for mediating its pro-survival effects.
Published Version: doi:10.1371/journal.pone.0005877
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691576/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4879208
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