p53-Mediated Tumor Suppression : DNA-Damage Response and Alternative Mechanisms
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Link zur Lizenz
EU-Projektnummer
DFG-Projektnummer
Projekt
Open Access-Veröffentlichung
Sammlungen
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
The tumor suppressor p53 regulates different cellular pathways involved in cell survival, DNA repair, apoptosis, and senescence. However, according to an increasing number of studies, the p53-mediated canonical DNA damage response is dispensable for tumor suppression. p53 is involved in mechanisms regulating many other cellular processes, including metabolism, autophagy, and cell migration and invasion, and these pathways might crucially contribute to its tumor suppressor function. In this review we summarize the canonical and non-canonical functions of p53 in an attempt to provide an overview of the potentially crucial aspects related to its tumor suppressor activity.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
PITOLLI, Consuelo, Ying WANG, Eleonora CANDI, Yufang SHI, Gerry MELINO, Ivano AMELIO, 2019. p53-Mediated Tumor Suppression : DNA-Damage Response and Alternative Mechanisms. In: Cancers. MDPI. 2019, 11(12), 1983. ISSN 2072-6694. eISSN 2072-6694. Available under: doi: 10.3390/cancers11121983BibTex
@article{Pitolli2019p53Me-57164, year={2019}, doi={10.3390/cancers11121983}, title={p53-Mediated Tumor Suppression : DNA-Damage Response and Alternative Mechanisms}, number={12}, volume={11}, issn={2072-6694}, journal={Cancers}, author={Pitolli, Consuelo and Wang, Ying and Candi, Eleonora and Shi, Yufang and Melino, Gerry and Amelio, Ivano}, note={Article Number: 1983} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/57164"> <dc:contributor>Wang, Ying</dc:contributor> <dcterms:issued>2019</dcterms:issued> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:creator>Amelio, Ivano</dc:creator> <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/"/> <dc:creator>Shi, Yufang</dc:creator> <dc:creator>Wang, Ying</dc:creator> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/57164"/> <dc:contributor>Shi, Yufang</dc:contributor> <dc:creator>Melino, Gerry</dc:creator> <dc:contributor>Melino, Gerry</dc:contributor> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2022-04-05T08:32:48Z</dc:date> <dc:rights>Attribution 4.0 International</dc:rights> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/57164/1/Pitolli_2-1uuvjsolnkug76.pdf"/> <dc:contributor>Pitolli, Consuelo</dc:contributor> <dc:contributor>Candi, Eleonora</dc:contributor> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/57164/1/Pitolli_2-1uuvjsolnkug76.pdf"/> <dc:creator>Candi, Eleonora</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/43"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/43"/> <dc:language>eng</dc:language> <dcterms:abstract xml:lang="eng">The tumor suppressor p53 regulates different cellular pathways involved in cell survival, DNA repair, apoptosis, and senescence. However, according to an increasing number of studies, the p53-mediated canonical DNA damage response is dispensable for tumor suppression. p53 is involved in mechanisms regulating many other cellular processes, including metabolism, autophagy, and cell migration and invasion, and these pathways might crucially contribute to its tumor suppressor function. In this review we summarize the canonical and non-canonical functions of p53 in an attempt to provide an overview of the potentially crucial aspects related to its tumor suppressor activity.</dcterms:abstract> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2022-04-05T08:32:48Z</dcterms:available> <dc:contributor>Amelio, Ivano</dc:contributor> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Pitolli, Consuelo</dc:creator> <dcterms:title>p53-Mediated Tumor Suppression : DNA-Damage Response and Alternative Mechanisms</dcterms:title> </rdf:Description> </rdf:RDF>