ABCB1, ABCG2, ABCC1, ABCC2, and ABCC3 drug transporter polymorphisms and their impact on drug bioavailability: what is our current understanding?

H Bruckmueller, I Cascorbi - Expert opinion on drug metabolism & …, 2021 - Taylor & Francis
Introduction Interindividual differences in drug response are a frequent clinical challenge
partly due to variation in pharmacokinetics. ATP-binding cassette (ABC) transporters are …

Pregnane X receptor (PXR) polymorphisms and cancer treatment

A Skandalaki, P Sarantis, S Theocharis - Biomolecules, 2021 - mdpi.com
Pregnane X Receptor (PXR) belongs to the nuclear receptors' superfamily and mainly
functions as a xenobiotic sensor activated by a variety of ligands. PXR is widely expressed …

Antiretroviral drug transporters and metabolic enzymes in human testicular tissue: potential contribution to HIV-1 sanctuary site

Y Huang, MT Hoque, MA Jenabian… - Journal of …, 2016 - academic.oup.com
Objectives The testes are a potential viral sanctuary site for HIV-1 infection. Our study aims
to provide insight into the expression and localization of key drug transporters and metabolic …

Intestinal and hepatic drug transporters: pharmacokinetic, pathophysiological, and pharmacogenetic roles

T Terada, D Hira - Journal of gastroenterology, 2015 - Springer
The efficacy and safety of pharmacotherapies are determined by the complex processes
involved in the interactions between drugs with the human body, including pharmacokinetic …

Genetic variations of the xenoreceptors NR1I2 and NR1I3 and their effect on drug disposition and response variability

LC Mbatchi, JP Brouillet, A Evrard - Pharmacogenomics, 2018 - Taylor & Francis
NR1I2 (PXR) and NR1I3 (CAR) are nuclear receptors that are classified as xenoreceptors.
Upon activation by various xenobiotics, including marketed drugs, they regulate the …

Genetic polymorphisms affecting the pharmacokinetics of antiretroviral drugs

A Calcagno, J Cusato, A D'Avolio, S Bonora - Clinical pharmacokinetics, 2017 - Springer
Background Antiretroviral treatment is highly effective in enhancing HIV-positive patients'
survival and quality of life. Despite an increased tolerability in recent years, a substantial …

An UPLC–MS/MS method coupled with automated on-line SPE for quantification of tacrolimus in peripheral blood mononuclear cells

D Pensi, A De Nicolò, M Pinon, PL Calvo… - … of Pharmaceutical and …, 2015 - Elsevier
Background Tacrolimus is an immunosuppressor used to treat patients undergoing liver
transplantation. TDM of hematic tacrolimus by liquid chromatography became standard …

A UPLC-MS-MS method for the simultaneous quantification of first-line antituberculars in plasma and in PBMCs

L Baietto, A Calcagno, I Motta, K Baruffi… - Journal of …, 2015 - academic.oup.com
Objectives TB is currently the second cause of death among patients affected with infectious
diseases. Quantification of drug levels in plasma and in cells where Mycobacterium …

Heme oxygenase-1-derived bilirubin counteracts HIV protease inhibitor-mediated endothelial cell dysfunction

XM Liu, ZE Durante, KJ Peyton, W Durante - Free Radical Biology and …, 2016 - Elsevier
The use of HIV protease inhibitors (PIs) has extended the duration and quality of life for HIV-
positive individuals. However there is increasing concern that this antiviral therapy may …

Nuclear receptors and drug metabolism for the personalization of cancer therapy

E Cecchin, E De Mattia, G Toffoli - Expert opinion on drug …, 2016 - Taylor & Francis
Introduction: A remarkable inter-individual variability in the occurrence of severe side effects
represents an ongoing challenge in cancer treatment. Significant research efforts have …