The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses

The tumor suppressor p53 is activated upon multiple cellular stresses, including DNA damage, oncogene activation, ribosomal stress, and hypoxia, to induce cell cycle arrest, apoptosis, and senescence. Mammalian target of rapamycin (mTOR), an evolutionarily conserved serine/threonine protein kinase,...

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Autores principales: Danrui Cui, Ruirui Qu, Dian Liu, Xiufang Xiong, Tingbo Liang, Yongchao Zhao
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Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/be8243f9ca5a43928a5ffb34f1562e53
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spelling oai:doaj.org-article:be8243f9ca5a43928a5ffb34f1562e532021-11-18T16:44:22ZThe Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses2296-634X10.3389/fcell.2021.775507https://doaj.org/article/be8243f9ca5a43928a5ffb34f1562e532021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.775507/fullhttps://doaj.org/toc/2296-634XThe tumor suppressor p53 is activated upon multiple cellular stresses, including DNA damage, oncogene activation, ribosomal stress, and hypoxia, to induce cell cycle arrest, apoptosis, and senescence. Mammalian target of rapamycin (mTOR), an evolutionarily conserved serine/threonine protein kinase, serves as a central regulator of cell growth, proliferation, and survival by coordinating nutrients, energy, growth factors, and oxygen levels. p53 dysfunction and mTOR pathway hyperactivation are hallmarks of human cancer. The balance between response to stresses or commitment to cell proliferation and survival is governed by various regulatory loops between the p53 and mTOR pathways. In this review, we first briefly introduce the tumor suppressor p53 and then describe the upstream regulators and downstream effectors of the mTOR pathway. Next, we discuss the role of p53 in regulating the mTOR pathway through its transcriptional and non-transcriptional effects. We further describe the complicated role of the mTOR pathway in modulating p53 activity. Finally, we discuss the current knowledge and future perspectives on the coordinated regulation of the p53 and mTOR pathways.Danrui CuiDanrui CuiDanrui CuiRuirui QuRuirui QuRuirui QuDian LiuDian LiuDian LiuXiufang XiongXiufang XiongTingbo LiangTingbo LiangTingbo LiangYongchao ZhaoYongchao ZhaoYongchao ZhaoYongchao ZhaoFrontiers Media S.A.articlep53mTORtranscriptionmiRNAtumorigenesisMDM2Biology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic p53
mTOR
transcription
miRNA
tumorigenesis
MDM2
Biology (General)
QH301-705.5
spellingShingle p53
mTOR
transcription
miRNA
tumorigenesis
MDM2
Biology (General)
QH301-705.5
Danrui Cui
Danrui Cui
Danrui Cui
Ruirui Qu
Ruirui Qu
Ruirui Qu
Dian Liu
Dian Liu
Dian Liu
Xiufang Xiong
Xiufang Xiong
Tingbo Liang
Tingbo Liang
Tingbo Liang
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
description The tumor suppressor p53 is activated upon multiple cellular stresses, including DNA damage, oncogene activation, ribosomal stress, and hypoxia, to induce cell cycle arrest, apoptosis, and senescence. Mammalian target of rapamycin (mTOR), an evolutionarily conserved serine/threonine protein kinase, serves as a central regulator of cell growth, proliferation, and survival by coordinating nutrients, energy, growth factors, and oxygen levels. p53 dysfunction and mTOR pathway hyperactivation are hallmarks of human cancer. The balance between response to stresses or commitment to cell proliferation and survival is governed by various regulatory loops between the p53 and mTOR pathways. In this review, we first briefly introduce the tumor suppressor p53 and then describe the upstream regulators and downstream effectors of the mTOR pathway. Next, we discuss the role of p53 in regulating the mTOR pathway through its transcriptional and non-transcriptional effects. We further describe the complicated role of the mTOR pathway in modulating p53 activity. Finally, we discuss the current knowledge and future perspectives on the coordinated regulation of the p53 and mTOR pathways.
format article
author Danrui Cui
Danrui Cui
Danrui Cui
Ruirui Qu
Ruirui Qu
Ruirui Qu
Dian Liu
Dian Liu
Dian Liu
Xiufang Xiong
Xiufang Xiong
Tingbo Liang
Tingbo Liang
Tingbo Liang
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
author_facet Danrui Cui
Danrui Cui
Danrui Cui
Ruirui Qu
Ruirui Qu
Ruirui Qu
Dian Liu
Dian Liu
Dian Liu
Xiufang Xiong
Xiufang Xiong
Tingbo Liang
Tingbo Liang
Tingbo Liang
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
Yongchao Zhao
author_sort Danrui Cui
title The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
title_short The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
title_full The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
title_fullStr The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
title_full_unstemmed The Cross Talk Between p53 and mTOR Pathways in Response to Physiological and Genotoxic Stresses
title_sort cross talk between p53 and mtor pathways in response to physiological and genotoxic stresses
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/be8243f9ca5a43928a5ffb34f1562e53
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