Biomarkers of early genotoxicity and oxidative stress for occupational risk assessment of exposure to styrene in the fibreglass reinforced plastic industry

2018 ◽  
Vol 298 ◽  
pp. 53-59 ◽  
Author(s):  
Delia Cavallo ◽  
Giovanna Tranfo ◽  
Cinzia Lucia Ursini ◽  
Anna Maria Fresegna ◽  
Aureliano Ciervo ◽  
...  
Mutagenesis ◽  
2008 ◽  
Vol 24 (2) ◽  
pp. 143-148 ◽  
Author(s):  
F. Rombaldi ◽  
C. Cassini ◽  
M. Salvador ◽  
J. Saffi ◽  
B. Erdtmann

2006 ◽  
Vol 164 ◽  
pp. S5-S6
Author(s):  
Takeki Uehara ◽  
Naoki Kiyosawa ◽  
Atsushi Ono ◽  
Toshikazu Miyagishima ◽  
Tetsuro Urushidani ◽  
...  

2015 ◽  
Vol 97 (5) ◽  
pp. 634-639 ◽  
Author(s):  
Qaisar Mahmood ◽  
Jin Wang ◽  
Arshid Pervez ◽  
Syeda Shaima Meryem ◽  
Muhammad Waseem ◽  
...  

Author(s):  
Carina Cassini ◽  
Caroline Calloni ◽  
Giovana Bortolini ◽  
Solange Garcia ◽  
Marco Dornelles ◽  
...  

Abstract


Author(s):  
Giulia Callegaro ◽  
Steven J. Kunnen ◽  
Panuwat Trairatphisan ◽  
Solène Grosdidier ◽  
Marije Niemeijer ◽  
...  

AbstractMechanism-based risk assessment is urged to advance and fully permeate into current safety assessment practices, possibly at early phases of drug safety testing. Toxicogenomics is a promising source of mechanisms-revealing data, but interpretative analysis tools specific for the testing systems (e.g. hepatocytes) are lacking. In this study, we present the TXG-MAPr webtool (available at https://txg-mapr.eu/WGCNA_PHH/TGGATEs_PHH/), an R-Shiny-based implementation of weighted gene co-expression network analysis (WGCNA) obtained from the Primary Human Hepatocytes (PHH) TG-GATEs dataset. The 398 gene co-expression networks (modules) were annotated with functional information (pathway enrichment, transcription factor) to reveal their mechanistic interpretation. Several well-known stress response pathways were captured in the modules, were perturbed by specific stressors and showed preservation in rat systems (rat primary hepatocytes and rat in vivo liver), with the exception of DNA damage and oxidative stress responses. A subset of 87 well-annotated and preserved modules was used to evaluate mechanisms of toxicity of endoplasmic reticulum (ER) stress and oxidative stress inducers, including cyclosporine A, tunicamycin and acetaminophen. In addition, module responses can be calculated from external datasets obtained with different hepatocyte cells and platforms, including targeted RNA-seq data, therefore, imputing biological responses from a limited gene set. As another application, donors’ sensitivity towards tunicamycin was investigated with the TXG-MAPr, identifying higher basal level of intrinsic immune response in donors with pre-existing liver pathology. In conclusion, we demonstrated that gene co-expression analysis coupled to an interactive visualization environment, the TXG-MAPr, is a promising approach to achieve mechanistic relevant, cross-species and cross-platform evaluation of toxicogenomic data.


Author(s):  
Hasan Haci Yeter ◽  
Berfu Korucu ◽  
Elif Burcu Bali ◽  
Ulver Derici

Abstract. Background: The pathophysiological basis of chronic kidney disease and its complications, including cardiovascular disease, are associated with chronic inflammation and oxidative stress. We investigated the effects of active vitamin D (calcitriol) and synthetic vitamin D analog (paricalcitol) on oxidative stress in hemodialysis patients. Methods: This cross-sectional study was composed of 83 patients with a minimum hemodialysis vintage of one year. Patients with a history of any infection, malignancy, and chronic inflammatory disease were excluded. Oxidative markers (total oxidant and antioxidant status) and inflammation markers (C-reactive protein and interleukin-6) were analyzed. Results: A total of 47% (39/83) patients were using active or analog vitamin D. Total antioxidant status was significantly higher in patients with using active or analog vitamin D than those who did not use (p = 0.006). Whereas, total oxidant status and oxidative stress index were significantly higher in patients with not using vitamin D when compared with the patients who were using vitamin D preparation (p = 0.005 and p = 0.004, respectively). On the other hand, total antioxidant status, total oxidant status, and oxidative stress index were similar between patients who used active vitamin D or vitamin D analog (p = 0.6; p = 0.4 and p = 0.7, respectively). Conclusion: The use of active or selective vitamin D analog in these patients decreases total oxidant status and increases total antioxidant status. Also, paricalcitol is as effective as calcitriol in decreasing total oxidant status and increasing total antioxidant status in patients with chronic kidney disease.


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