C‐Jun N‐terminal kinase signalling pathway in response to cisplatin

D Yan, GY An, MT Kuo - Journal of cellular and molecular …, 2016 - Wiley Online Library
Cisplatin (cis diamminedichloroplatinum II, cDDP) is one of the most effective cancer
chemotherapeutic agents and is used in the treatment of many types of human …

Environmental risk assessment of widely used anticancer drugs (5-fluorouracil, cisplatin, etoposide, imatinib mesylate)

M Mišík, M Filipic, A Nersesyan, M Kundi, M Isidori… - Water research, 2019 - Elsevier
Anticancer drugs are among the most toxic chemicals, which are commercially produced;
therefore, their release in aquatic ecosystems raised concerns in regard to potential adverse …

Development of in vitro 3D cell model from hepatocellular carcinoma (HepG2) cell line and its application for genotoxicity testing

M Štampar, J Tomc, M Filipič, B Žegura - Archives of Toxicology, 2019 - Springer
The evaluation of genotoxicity plays an important role within hazard identification and risk
assessment of chemicals and consumer products. For genotoxicity assessment, in vitro …

Detection of anti-cancer drugs and metabolites in the effluents from a large Brazilian cancer hospital and an evaluation of ecotoxicology

M de Oliveira Klein, SV Serrano, Á Santos-Neto… - Environmental …, 2021 - Elsevier
The use of chemotherapy agents has been growing worldwide, due to the increase number
of cancer cases. In several countries, mainly in Europe countries, these drugs have been …

Anti-cancer drugs in aquatic environment can cause cancer: insight about mutagenicity in tadpoles

AP da Costa Araújo, C Mesak, MF Montalvão… - Science of the Total …, 2019 - Elsevier
Abstract Cyclophosphamide (Cyc) and 5-fluorouracil (5-FU) are two of the most used
antineoplastic drugs (AD) in the world. However, their discharge in the environment became …

Acute aquatic toxicity assessment of six anti-cancer drugs and one metabolite using biotest battery–biological effects and stability under test conditions

A Białk-Bielińska, E Mulkiewicz, M Stokowski, S Stolte… - Chemosphere, 2017 - Elsevier
Available ecotoxicological data for anti-cancer drugs and their metabolites are incomplete,
and only some studies have been accompanied by chemical analysis. Therefore, the main …

Analysis of molecular mechanisms of 5-fluorouracil-induced steatosis and inflammation in vitro and in mice

J Sommer, A Mahli, K Freese, TS Schiergens… - …, 2016 - pmc.ncbi.nlm.nih.gov
Chemotherapy-associated steatohepatitis is attracting increasing attention because it
heralds an increased risk of morbidity and mortality in patients undergoing surgery because …

Toxicogenomic responses of low level anticancer drug exposures in Daphnia magna

C Russo, M Isidori, JA Deaver, HC Poynton - Aquatic Toxicology, 2018 - Elsevier
The use of anticancer drugs in chemotherapy is increasing, leading to growing
environmental concentrations of imatinib mesylate (IMA), cisplatinum (CDDP), and …

Antiproliferative chromone derivatives induce K562 cell death through endogenous and exogenous pathways

R Jiao, F Xu, X Huang, H Li, W Liu, H Cao… - Journal of Enzyme …, 2020 - Taylor & Francis
A series of furoxan derivatives of chromone were prepared. The antiproliferative activities
were tested against five cancer cell lines HepG2, MCF-7, HCT-116, B16, and K562, and two …

Adverse toxic effects of tyrosine kinase inhibitors on non-target zebrafish liver (ZFL) cells

K Kološa, B Žegura, M Štampar, M Filipič… - International Journal of …, 2023 - mdpi.com
Over the past 20 years, numerous tyrosine kinase inhibitors (TKIs) have been introduced for
targeted therapy of various types of malignancies. Due to frequent and increasing use …