Download
Upload.pdf 2,13MB
WeightNameValue
1000 Titel
  • SAMHD1 in cancer: curse or cure?
1000 Autor/in
  1. Schott, Kerstin |
  2. Majer, Catharina |
  3. Bulashevska, Alla |
  4. Childs, Liam |
  5. Schmidt, Mirko Hans Heinrich |
  6. Rajalingam, Krishnaraj |
  7. Munder, Markus |
  8. König, Renate |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-09-04
1000 Erschienen in
1000 Quellenangabe
  • 100(3):351-372
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00109-021-02131-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843919/ |
1000 Ergänzendes Material
  • https://link.springer.com/article/10.1007/s00109-021-02131-w#Sec14 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Human sterile α motif and HD domain-containing protein 1 (SAMHD1), originally described as the major cellular deoxyribonucleoside triphosphate triphosphohydrolase (dNTPase) balancing the intracellular deoxynucleotide (dNTP) pool, has come recently into focus of cancer research. As outlined in this review, SAMHD1 has been reported to be mutated in a variety of cancer types and the expression of SAMHD1 is dysregulated in many cancers. Therefore, SAMHD1 is regarded as a tumor suppressor in certain tumors. Moreover, it has been proposed that SAMHD1 might fulfill the requirements of a driver gene in tumor development or might promote a so-called mutator phenotype. Besides its role as a dNTPase, several novel cellular functions of SAMHD1 have come to light only recently, including a role as negative regulator of innate immune responses and as facilitator of DNA end resection during DNA replication and repair. Therefore, SAMHD1 can be placed at the crossroads of various cellular processes. The present review summarizes the negative role of SAMHD1 in chemotherapy sensitivity, highlights reported SAMHD1 mutations found in various cancer types, and aims to discuss functional consequences as well as underlying mechanisms of SAMHD1 dysregulation potentially involved in cancer development.
1000 Sacherschließung
lokal dNTP regulation
lokal Mutations in SAMHD1
lokal Cellular functions of SAMHD1
gnd 4543844-4 Molekulare Medizin
lokal Cancer development
lokal SAMHD1
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://d-nb.info/gnd/1167343417|https://frl.publisso.de/adhoc/uri/IE1hamVyLCBDYXRoYXJpbmEgICA=|https://orcid.org/0000-0001-9900-5693|https://orcid.org/0000-0002-2080-1804|https://d-nb.info/gnd/123687497|https://orcid.org/0000-0002-4175-9633|https://orcid.org/0000-0003-4947-8796|https://orcid.org/0000-0003-4882-9179
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft |
  2. Projekt DEAL |
1000 Fördernummer
  1. TP09; TP05; TP06; TP04
  2. -
1000 Förderprogramm
  1. Collaborative Research Center 1292
  2. Open access funding
1000 Dateien
  1. SAMHD1 in cancer: curse or cure?
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Deutsche Forschungsgemeinschaft |
    1000 Förderprogramm Collaborative Research Center 1292
    1000 Fördernummer TP09; TP05; TP06; TP04
  2. 1000 joinedFunding-child
    1000 Förderer Projekt DEAL |
    1000 Förderprogramm Open access funding
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6432229.rdf
1000 Erstellt am 2022-03-15T10:25:52.097+0100
1000 Erstellt von 323
1000 beschreibt frl:6432229
1000 Bearbeitet von 317
1000 Zuletzt bearbeitet 2022-04-27T15:27:42.649+0200
1000 Objekt bearb. Wed Apr 27 15:27:30 CEST 2022
1000 Vgl. frl:6432229
1000 Oai Id
  1. oai:frl.publisso.de:frl:6432229 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

View source