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Abstract
Disruption of cellular timekeeping systems is a key driver of cancer cell development and progression.
- Circadian rhythms are regulated by core clock genes, including CLOCK, BMAL1, PER, and CRY.
- Altered circadian rhythms can lead to changes in gene expression, resulting in excessive cell growth and genetic instability.
- Cancer cells exhibit enhanced glycolysis, lipid production, and altered mitochondrial activity, processes typically regulated by the circadian clock.
- Irregular functioning of clock genes is associated with metabolic changes that support tumor development and survival.
- Circadian disruption may enhance metastatic progression by influencing tumor angiogenesis, inflammation, and immune responses.
- Chronotherapy could increase the efficacy of cancer treatments while reducing toxicity by aligning therapies with biological rhythms.
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