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p53 mRNA Metabolism Links with the DNA Damage Response
S. Vadivel Gnanasundram, O. Bonczek, L. Wang, S. Chen, R. Fahraeus
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
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PubMed
34573428
DOI
10.3390/genes12091446
Knihovny.cz E-resources
- MeSH
- Humans MeSH
- RNA, Messenger metabolism MeSH
- Mutation MeSH
- Tumor Suppressor Protein p53 genetics metabolism MeSH
- Untranslated Regions MeSH
- DNA Repair * physiology MeSH
- DNA Damage * MeSH
- RNA-Binding Proteins genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Human cells are subjected to continuous challenges by different genotoxic stress attacks. DNA damage leads to erroneous mutations, which can alter the function of oncogenes or tumor suppressors, resulting in cancer development. To circumvent this, cells activate the DNA damage response (DDR), which mainly involves cell cycle regulation and DNA repair processes. The tumor suppressor p53 plays a pivotal role in the DDR by halting the cell cycle and facilitating the DNA repair processes. Various pathways and factors participating in the detection and repair of DNA have been described, including scores of RNA-binding proteins (RBPs) and RNAs. It has become increasingly clear that p53's role is multitasking, and p53 mRNA regulation plays a prominent part in the DDR. This review is aimed at covering the p53 RNA metabolism linked to the DDR and highlights the recent findings.
Department of Medical Biosciences Umeå University 901 87 Umeå Sweden
International Centre for Cancer Vaccine Science University of Gdansk 80 822 Gdansk Poland
RECAMO Masaryk Memorial Cancer Institute Zluty Kopec 7 656 53 Brno Czech Republic
References provided by Crossref.org
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