Adrenocortical carcinoma

T Else, AC Kim, A Sabolch, VM Raymond… - Endocrine …, 2014 - academic.oup.com
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy, often with an unfavorable
prognosis. Here we summarize the knowledge about diagnosis, epidemiology …

Oxysterols: From cholesterol metabolites to key mediators

V Mutemberezi, O Guillemot-Legris… - Progress in lipid research, 2016 - Elsevier
Oxysterols are cholesterol metabolites that can be produced through enzymatic or radical
processes. They constitute a large family of lipids (ie the oxysterome) involved in a plethora …

Cyp2c70 is responsible for the species difference in bile acid metabolism between mice and humans [S]

S Takahashi, T Fukami, Y Masuo, CN Brocker, C **e… - Journal of lipid …, 2016 - jlr.org
Bile acids are synthesized from cholesterol in the liver and subjected to multiple metabolic
biotransformations in hepatocytes, including oxidation by cytochromes P450 (CYPs) and …

Human cytochromes P450 in health and disease

DW Nebert, K Wikvall, WL Miller - … Transactions of the …, 2013 - royalsocietypublishing.org
There are 18 mammalian cytochrome P450 (CYP) families, which encode 57 genes in the
human genome. CYP2, CYP3 and CYP4 families contain far more genes than the other 15 …

[HTML][HTML] Current challenges and future perspectives in oral absorption research: An opinion of the UNGAP network

Z Vinarov, B Abrahamsson, P Artursson… - Advanced drug delivery …, 2021 - Elsevier
Although oral drug delivery is the preferred administration route and has been used for
centuries, modern drug discovery and development pipelines challenge conventional …

[HTML][HTML] Preclinical experimental models of drug metabolism and disposition in drug discovery and development

D Zhang, G Luo, X Ding, C Lu - Acta Pharmaceutica Sinica B, 2012 - Elsevier
Drug discovery and development involve the utilization of in vitro and in vivo experimental
models. Different models, ranging from test tube experiments to cell cultures, animals …

Discovery and characterization of potent dual P-glycoprotein and CYP3A4 inhibitors: design, synthesis, cryo-EM analysis, and biological evaluations

S Urgaonkar, K Nosol, AM Said… - Journal of Medicinal …, 2021 - ACS Publications
Targeted concurrent inhibition of intestinal drug efflux transporter P-glycoprotein (P-gp) and
drug metabolizing enzyme cytochrome P450 3A4 (CYP3A4) is a promising approach to …

Docetaxel microemulsion for enhanced oral bioavailability: preparation and in vitro and in vivo evaluation

YM Yin, FD Cui, CF Mu, MK Choi, JS Kim… - Journal of Controlled …, 2009 - Elsevier
A microemulsion system of docetaxel was prepared and evaluated for its solubilization
capacity and oral bioavailability improvement. Based on a solubility study and pseudo …

[HTML][HTML] An update on the role of intestinal cytochrome P450 enzymes in drug disposition

F **e, X Ding, QY Zhang - Acta Pharmaceutica Sinica B, 2016 - Elsevier
Oral administration is the most commonly used route for drug treatment. Intestinal
cytochrome P450 (CYP)-mediated metabolism can eliminate a large proportion of some …

Improvement of cellular uptake, in vitro antitumor activity and sustained release profile with increased bioavailability from a nanoemulsion platform

H Choudhury, B Gorain, S Karmakar, E Biswas… - International journal of …, 2014 - Elsevier
Paclitaxel, a potential anticancer agent against solid tumors has been restricted from its oral
use due to poor water solubility as well as Pgp efflux property. The present study was aimed …