4.3 Review

Chrono-Drug Discovery and Development Based on Circadian Rhythm of Molecular, Cellular and Organ Level

Journal

BIOLOGICAL & PHARMACEUTICAL BULLETIN
Volume 44, Issue 6, Pages 747-761

Publisher

PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/bpb.b21-00277

Keywords

circadian rhythm; molecular clock; chronopharmacokinetics; chronopharmacology; chronotherapy

Funding

  1. Platform Project for Supporting Drug Discovery and Life Science Research [Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)] from AMED [JP20am0101091, JP21am0101091]

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This study focuses on the role of the molecular clock in regulating circadian rhythms and related disease treatments, emphasizing the importance of gene and antibody delivery as well as targeted therapy for specific disease molecules. New drugs targeting the molecular clock show potential in human disease treatments, and research on chronic kidney disease has revealed new molecular mechanisms.
The paired suprachiasmatic nuclei (SCN) is the circadian pacemaker in mammals. Clock genes ultimately regulates a vast array of circadian rhythms involved in biological, physiological and behavioral process. The clock genes are closely related to sleep disorders, metabolic syndromes, and cancer diseases. Monitoring rhythm, overcoming rhythm disruption, and manipulating rhythm from the perspective of the clock genes play an important role to improve chronopharmacotherapy. Such an approach should be achieved by overcoming the new challenges in drug delivery systems that match the circadian rhythm (Chrono-DDS). Gene and antibody delivery, targeting specific molecules for certain diseases have been focused in recent studies on pharmacotherapy. One of important candidates should also be clock genes. New drugs targeting the molecular clock are being developed to manage diseases in humans. The circadian dynamics of cancer stem cells are controlled by the tumor microenvironment and provide proof for its implication in chronotherapy against triple- negative breast cancer. To examine the relationship between the circadian clock and chronic kidney disease (CKD) exacervation leads to clarify the novel molecular mechanisms causing renal malfunction in mice with CKD. A novel inhibitor of cell cycle regulatory factors has been identified and the inhibitor repressed renal inflammation in a CKD mouse model. Therefore, this review aims to introduce the role of the molecular clock in the time-dependent dosing changes in the therapeutic effect and safety of a drug and the possibility of drug discovery and development based on the molecular clock.

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