p53 represses the mevalonate pathway to mediate tumor suppression

Summary. There are still gaps in our understanding of the complex processes by which p53 suppresses tumorigenesis. Here we describe a novel role for p53 in suppressing the mevalonate pathway, which is responsible for biosynthesis of cholesterol and nonsterol isoprenoids. p53 blocks activation of SRE...

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Main Authors: Moon, Sung-Hwan (Author) , Tschaharganeh, Darjus-Felix (Author)
Format: Article (Journal)
Language:English
Published: 2019
In: Cell
Year: 2018, Volume: 176, Issue: 3, Pages: 564-580
ISSN:1097-4172
DOI:10.1016/j.cell.2018.11.011
Online Access:Verlag, Volltext: http://dx.doi.org/10.1016/j.cell.2018.11.011
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0092867418315034
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Author Notes:Sung-Hwan Moon, Chun-Hao Huang, Shauna L. Houlihan, Kausik Regunath, William A. Freed-Pastor, John P. Morris, Darjus F. Tschaharganeh, Edward R. Kastenhuber, Anthony M. Barsotti, Rachel Culp-Hill, Wen Xue, Yu-Jui Ho, Timour Baslan, Xiang Li, Allison Mayle, Elisa de Stanchina, Lars Zender, David R. Tong, Angelo D’Alessandro, Scott W. Lowe, and Carol Prives

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520 |a Summary. There are still gaps in our understanding of the complex processes by which p53 suppresses tumorigenesis. Here we describe a novel role for p53 in suppressing the mevalonate pathway, which is responsible for biosynthesis of cholesterol and nonsterol isoprenoids. p53 blocks activation of SREBP-2, the master transcriptional regulator of this pathway, by transcriptionally inducing the ABCA1 cholesterol transporter gene. A mouse model of liver cancer reveals that downregulation of mevalonate pathway gene expression by p53 occurs in premalignant hepatocytes, when p53 is needed to actively suppress tumorigenesis. Furthermore, pharmacological or RNAi inhibition of the mevalonate pathway restricts the development of murine hepatocellular carcinomas driven by p53 loss. Like p53 loss, ablation of ABCA1 promotes murine liver tumorigenesis and is associated with increased SREBP-2 maturation. Our findings demonstrate that repression of the mevalonate pathway is a crucial component of p53-mediated liver tumor suppression and outline the mechanism by which this occurs. 
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