[HTML][HTML] Drug repurposing in oncology: Compounds, pathways, phenotypes and computational approaches for colorectal cancer

P Nowak-Sliwinska, L Scapozza, AR i Altaba - Biochimica et Biophysica …, 2019 - Elsevier
The strategy of using existing drugs originally developed for one disease to treat other
indications has found success across medical fields. Such drug repurposing promises faster …

Large-scale prediction and testing of drug activity on side-effect targets

E Lounkine, MJ Keiser, S Whitebread, D Mikhailov… - Nature, 2012 - nature.com
Discovering the unintended 'off-targets' that predict adverse drug reactions is daunting by
empirical methods alone. Drugs can act on several protein targets, some of which can be …

Quo vadis blood protein adductomics?

G Sabbioni, BW Day - Archives of toxicology, 2022 - Springer
Chemicals are measured regularly in air, food, the environment, and the workplace.
Biomonitoring of chemicals in biological fluids is a tool to determine the individual exposure …

Biomonitoring human albumin adducts: the past, the present, and the future

G Sabbioni, RJ Turesky - Chemical research in toxicology, 2017 - ACS Publications
Serum albumin (Alb) is the most abundant protein in blood plasma. Alb reacts with many
carcinogens and/or their electrophilic metabolites. Studies conducted over 20 years ago …

Hepatotoxic evaluation of toosendanin via biomarker quantification and pathway map** of large-scale chemical proteomics

Y Zhuo, Y Zhang, M Li, H Wu, S Gong, X Hu… - Food and Chemical …, 2021 - Elsevier
Drug-induced liver injury (DILI) is a major side effect, sometimes can't be exactly evaluated
by current approaches partly as the covalent modification of drug or its reactive metabolites …

Animal models of idiosyncratic drug reactions

W Ng, ARM Lobach, X Zhu, X Chen, F Liu… - Advances in …, 2012 - Elsevier
If we could predict and prevent idiosyncratic drug reactions (IDRs) it would have a profound
effect on drug development and therapy. Given our present lack of mechanistic …

Detection of drug bioactivation in vivo: mechanism of nevirapine–albumin conjugate formation in patients

X Meng, A Howarth, CJ Earnshaw… - Chemical Research …, 2013 - ACS Publications
The non-nucleoside reverse transcriptase inhibitor nevirapine (NVP) is widely used for the
treatment of human immunodeficiency virus type 1 (HIV-1), particularly in develo** …

Evidence for nevirapine bioactivation in man: searching for the first step in the mechanism of nevirapine toxicity

U Caixas, AMM Antunes, AT Marinho, ALA Godinho… - Toxicology, 2012 - Elsevier
Despite its efficacy, including in the prevention of vertical transmission, the antiretroviral
nevirapine is associated with severe idiosyncratic hepatotoxicity and skin rash. The …

Hepatocyte spheroids as a competent in vitro system for drug biotransformation studies: nevirapine as a bioactivation case study

PF Pinheiro, SA Pereira, SG Harjivan, IL Martins… - Archives of …, 2017 - Springer
The development of metabolically competent in vitro models is of utmost importance for
predicting adverse drug reactions, thereby preventing attrition-related economical and …

Biomarker-based drug safety assessment in the age of systems pharmacology: from foundational to regulatory science

C Zhang, H Hong, DL Mendrick, Y Tang… - Biomarkers in …, 2015 - Taylor & Francis
Improved biomarker-based assessment of drug safety is needed in drug discovery and
development as well as regulatory evaluation. However, identifying drug safety-related …