The emerging role of the KCTD proteins in cancer.
BTB domain
Cancer
Cul3
KCASH family
KCTD family
KCTD15
Oncogene
Tumor suppressor
Ubiquitination
Journal
Cell communication and signaling : CCS
ISSN: 1478-811X
Titre abrégé: Cell Commun Signal
Pays: England
ID NLM: 101170464
Informations de publication
Date de publication:
17 05 2021
17 05 2021
Historique:
received:
04
12
2020
accepted:
05
04
2021
entrez:
18
5
2021
pubmed:
19
5
2021
medline:
27
1
2022
Statut:
epublish
Résumé
The human family of Potassium (K+) Channel Tetramerization Domain (KCTD) proteins counts 25 members, and a significant number of them are still only partially characterized. While some of the KCTDs have been linked to neurological disorders or obesity, a growing tally of KCTDs are being associated with cancer hallmarks or involved in the modulation of specific oncogenic pathways. Indeed, the potential relevance of the variegate KCTD family in cancer warrants an updated picture of the current knowledge and highlights the need for further research on KCTD members as either putative therapeutic targets, or diagnostic/prognostic markers. Homology between family members, capability to participate in ubiquitination and degradation of different protein targets, ability to heterodimerize between members, role played in the main signalling pathways involved in development and cancer, are all factors that need to be considered in the search for new key players in tumorigenesis. In this review we summarize the recent published evidence on KCTD members' involvement in cancer. Furthermore, by integrating this information with data extrapolated from public databases that suggest new potential associations with cancers, we hypothesize that the number of KCTD family members involved in tumorigenesis (either as positive or negative modulator) may be bigger than so far demonstrated. Video abstract.
Identifiants
pubmed: 34001146
doi: 10.1186/s12964-021-00737-8
pii: 10.1186/s12964-021-00737-8
pmc: PMC8127222
doi:
Substances chimiques
Potassium Channels, Voltage-Gated
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
56Subventions
Organisme : Sapienza Università di Roma
ID : Sapienza Research Grant
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