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Published on: September 28, 2017
Time to fight: targeting the circadian clock molecular machinery in cancer therapy
Matteo Astone1, Massimo M Santoro2
1Department of Biology, University of Padova, I-35131, Italy.
Abstract:
The circadian clock regulates a wide range of molecular pathways and biological processes. The expression of clock genes is often altered in cancer, fostering tumor initiation and progression. Inhibition and activation of core circadian clock genes, as well as treatments that restore circadian rhythmicity, have been successful in counteracting tumor growth in different experimental models. Here, we provide an up-to-date overview of studies that show the therapeutic effects of targeting the clock molecular machinery in cancer, both genetically and pharmacologically. We also highlight future areas for progress that offer a promising path towards innovative anticancer strategies. Substantial limitations in the current understanding of the complex interplay between the circadian clock and cancer in vivo need to be addressed in order to allow clock-targeting therapies in cancer.
Insights
Targeting the body's internal clock (circadian clock) shows promise for cancer treatment. Modulating clock genes and restoring rhythm can inhibit tumor growth, offering new therapeutic strategies.
Area of Science:
- * Chronobiology and Cancer Research
- * Molecular Oncology
- * Circadian Biology
Background:
- * The circadian clock governs numerous biological processes, and its disruption is linked to cancer development and progression.
- * Altered expression of core circadian clock genes is a hallmark of many cancers.
- * Existing research indicates that manipulating the circadian clock can impact tumor growth.
Purpose of the Study:
- * To provide a comprehensive review of therapeutic strategies targeting the molecular machinery of the circadian clock in cancer.
- * To summarize the efficacy of genetic and pharmacological interventions aimed at clock genes.
- * To identify future research directions for clock-targeting cancer therapies.
Main Methods:
- * Systematic literature review of preclinical and clinical studies.
- * Analysis of research on genetic and pharmacological targeting of circadian clock components.
- * Evaluation of studies investigating the restoration of circadian rhythmicity in cancer models.
Main Results:
- * Inhibition and activation of core circadian clock genes demonstrate efficacy in reducing tumor growth across various experimental models.
- * Treatments designed to restore circadian rhythmicity have shown success in counteracting cancer progression.
- * Both genetic and pharmacological approaches targeting the clock machinery offer therapeutic potential.
Conclusions:
- * Targeting the circadian clock represents a promising avenue for novel anticancer strategies.
- * Further research is needed to fully elucidate the complex in vivo interactions between the circadian clock and cancer.
- * Addressing current knowledge gaps is crucial for the clinical translation of clock-targeting therapies.
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