| Literature DB >> 33846572 |
Francesca Battaglin1, Priscilla Chan2, Yuanzhong Pan2, Shivani Soni1, Meng Qu2, Erin R Spiller3, Sofi Castanon1, Evanthia T Roussos Torres1, Shannon M Mumenthaler1,3, Steve A Kay2, Heinz-Josef Lenz4.
Abstract
Disruption of the cellular pathway modulating endogenous 24-h rhythms, referred to as "the circadian clock", has been recently proven to be associated with cancer risk, development, and progression. This pathway operates through a complex network of transcription-translation feedback loops generated by a set of interplaying proteins. The expression of core circadian clock genes is frequently dysregulated in human tumors; however, the specific effects and underlying mechanisms seem to vary depending on the cancer types and are not fully understood. In addition, specific oncogenes may differentially induce the dysregulation of the circadian clock in tumors. Pharmacological modulation of clock components has been shown to result in specific lethality in certain types of cancer cells, and thus holds great promise as a novel anti-cancer therapeutic approach. Here we present an overview of the rationale and current evidence for targeting the clock in cancer treatment.Entities:
Mesh:
Year: 2021 PMID: 33846572 PMCID: PMC8549632 DOI: 10.1038/s41388-021-01778-6
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867