TY - JOUR
T1 - Mapping genes for drug chronotherapy
AU - Wei, Kun
AU - Wang, Qian
AU - Gan, Jingwen
AU - Zhang, Shilong
AU - Ye, Meixia
AU - Gragnoli, Claudia
AU - Wu, Rongling
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/11
Y1 - 2018/11
N2 - Genome-wide association studies have been increasingly used to map and characterize genes that contribute to interindividual variation in drug response. Some studies have integrated the pharmacokinetic (PK) and pharmacodynamic (PD) processes of drug reactions into association mapping, gleaning new insight into how genes determine the dynamic relationship of drug effect and drug dose. Here, we present an evolutionary framework by which two distinct concepts, chronopharmacodynamics and heterochrony (describing variation in the timing and rate of developmental events), are married to comprehend the pharmacogenetic architecture of drug response. The resulting new concept, heterochronopharmacodynamics (HCPD), can better interpret how genes influence drug efficacy and drug toxicity according to the circadian rhythm of the body and changes in drug concentration.
AB - Genome-wide association studies have been increasingly used to map and characterize genes that contribute to interindividual variation in drug response. Some studies have integrated the pharmacokinetic (PK) and pharmacodynamic (PD) processes of drug reactions into association mapping, gleaning new insight into how genes determine the dynamic relationship of drug effect and drug dose. Here, we present an evolutionary framework by which two distinct concepts, chronopharmacodynamics and heterochrony (describing variation in the timing and rate of developmental events), are married to comprehend the pharmacogenetic architecture of drug response. The resulting new concept, heterochronopharmacodynamics (HCPD), can better interpret how genes influence drug efficacy and drug toxicity according to the circadian rhythm of the body and changes in drug concentration.
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U2 - 10.1016/j.drudis.2018.06.011
DO - 10.1016/j.drudis.2018.06.011
M3 - Review article
C2 - 29964181
AN - SCOPUS:85049607729
SN - 1359-6446
VL - 23
SP - 1883
EP - 1888
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 11
ER -