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p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression

The metabolic pathways through which p53 functions as a potent tumor suppressor are incompletely understood. Here we report that, by associating with the Vitamin D receptor (VDR), p53 induces numerous genes encoding enzymes for peroxisomal fatty acid β-oxidation (FAO). This leads to increased cytoso...

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Autores principales: Zhao, Jianhong, Zhou, Xiaojun, Chen, Baoxiang, Lu, Mingzhu, Wang, Genxin, Elumalai, Nagarajan, Tian, Chenhui, Zhang, Jinmiao, Liu, Yanliang, Chen, Zhiqiang, Zhou, Xinyi, Wu, Mingzhi, Li, Mengjiao, Prochownik, Edward V., Tavassoli, Ali, Jiang, Congqing, Li, Youjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905075/
https://www.ncbi.nlm.nih.gov/pubmed/36750554
http://dx.doi.org/10.1038/s41419-023-05625-2
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author Zhao, Jianhong
Zhou, Xiaojun
Chen, Baoxiang
Lu, Mingzhu
Wang, Genxin
Elumalai, Nagarajan
Tian, Chenhui
Zhang, Jinmiao
Liu, Yanliang
Chen, Zhiqiang
Zhou, Xinyi
Wu, Mingzhi
Li, Mengjiao
Prochownik, Edward V.
Tavassoli, Ali
Jiang, Congqing
Li, Youjun
author_facet Zhao, Jianhong
Zhou, Xiaojun
Chen, Baoxiang
Lu, Mingzhu
Wang, Genxin
Elumalai, Nagarajan
Tian, Chenhui
Zhang, Jinmiao
Liu, Yanliang
Chen, Zhiqiang
Zhou, Xinyi
Wu, Mingzhi
Li, Mengjiao
Prochownik, Edward V.
Tavassoli, Ali
Jiang, Congqing
Li, Youjun
author_sort Zhao, Jianhong
collection PubMed
description The metabolic pathways through which p53 functions as a potent tumor suppressor are incompletely understood. Here we report that, by associating with the Vitamin D receptor (VDR), p53 induces numerous genes encoding enzymes for peroxisomal fatty acid β-oxidation (FAO). This leads to increased cytosolic acetyl-CoA levels and acetylation of the enzyme 5-Aminoimidazole-4-Carboxamide Ribonucleotide Formyltransferase/IMP Cyclohydrolase (ATIC), which catalyzes the last two steps in the purine biosynthetic pathway. This acetylation step, mediated by lysine acetyltransferase 2B (KAT2B), occurs at ATIC Lys 266, dramatically inhibits ATIC activity, and inversely correlates with colorectal cancer (CRC) tumor growth in vitro and in vivo, and acetylation of ATIC is downregulated in human CRC samples. p53-deficient CRCs with high levels of ATIC is more susceptible to ATIC inhibition. Collectively, these findings link p53 to peroxisomal FAO, purine biosynthesis, and CRC pathogenesis in a manner that is regulated by the levels of ATIC acetylation.
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spelling pubmed-99050752023-02-08 p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression Zhao, Jianhong Zhou, Xiaojun Chen, Baoxiang Lu, Mingzhu Wang, Genxin Elumalai, Nagarajan Tian, Chenhui Zhang, Jinmiao Liu, Yanliang Chen, Zhiqiang Zhou, Xinyi Wu, Mingzhi Li, Mengjiao Prochownik, Edward V. Tavassoli, Ali Jiang, Congqing Li, Youjun Cell Death Dis Article The metabolic pathways through which p53 functions as a potent tumor suppressor are incompletely understood. Here we report that, by associating with the Vitamin D receptor (VDR), p53 induces numerous genes encoding enzymes for peroxisomal fatty acid β-oxidation (FAO). This leads to increased cytosolic acetyl-CoA levels and acetylation of the enzyme 5-Aminoimidazole-4-Carboxamide Ribonucleotide Formyltransferase/IMP Cyclohydrolase (ATIC), which catalyzes the last two steps in the purine biosynthetic pathway. This acetylation step, mediated by lysine acetyltransferase 2B (KAT2B), occurs at ATIC Lys 266, dramatically inhibits ATIC activity, and inversely correlates with colorectal cancer (CRC) tumor growth in vitro and in vivo, and acetylation of ATIC is downregulated in human CRC samples. p53-deficient CRCs with high levels of ATIC is more susceptible to ATIC inhibition. Collectively, these findings link p53 to peroxisomal FAO, purine biosynthesis, and CRC pathogenesis in a manner that is regulated by the levels of ATIC acetylation. Nature Publishing Group UK 2023-02-07 /pmc/articles/PMC9905075/ /pubmed/36750554 http://dx.doi.org/10.1038/s41419-023-05625-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhao, Jianhong
Zhou, Xiaojun
Chen, Baoxiang
Lu, Mingzhu
Wang, Genxin
Elumalai, Nagarajan
Tian, Chenhui
Zhang, Jinmiao
Liu, Yanliang
Chen, Zhiqiang
Zhou, Xinyi
Wu, Mingzhi
Li, Mengjiao
Prochownik, Edward V.
Tavassoli, Ali
Jiang, Congqing
Li, Youjun
p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title_full p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title_fullStr p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title_full_unstemmed p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title_short p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
title_sort p53 promotes peroxisomal fatty acid β-oxidation to repress purine biosynthesis and mediate tumor suppression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905075/
https://www.ncbi.nlm.nih.gov/pubmed/36750554
http://dx.doi.org/10.1038/s41419-023-05625-2
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