Assessing human exposure risk to cadmium through inhalation and seafood consumption

2012 ◽  
Vol 227-228 ◽  
pp. 353-361 ◽  
Author(s):  
Yun-Ru Ju ◽  
Wei-Yu Chen ◽  
Chung-Min Liao
Author(s):  
Shima Ziajahromi ◽  
Meysam Khanizadeh ◽  
Farhad Nejadkoorki
Keyword(s):  

2020 ◽  
Vol 201 ◽  
pp. 110833 ◽  
Author(s):  
Samantha Jiménez-Oyola ◽  
María-Jesús García-Martínez ◽  
Marcelo F. Ortega ◽  
David Bolonio ◽  
Clara Rodríguez ◽  
...  

2013 ◽  
Vol 316-317 ◽  
pp. 501-504
Author(s):  
Yan Hu ◽  
Yao Wang ◽  
Ze Sen Wang ◽  
Da Zhou Wang ◽  
Yu Li

To assess how the human exposure to environmental carcinogenic polycyclic aromatic hydrocarbons (PAHs) contaminant generated from a typical oilfield, we used a recommended exposure risk model, appraised with actual measured PAH concentration in an oilfield soils. Hierarchical clustering method was also applied to classfied the total exposure risk (carcinogenic and non-carcinogenic) of 16 PAHs, and four risk grades were obtained as zero risk, low risk, medium risk, and high risk. It was found that ingestion was the major exposure route among the three exposure routes. Risks of dibenz(a,h)anthracene and benzo(a)pyrene were higher than the other contaminants, and represent high risk grade.


2019 ◽  
Vol 19 (3) ◽  
pp. 206-214 ◽  
Author(s):  
Qinghua Wu ◽  
Jiri Patocka ◽  
Kamil Kuca

Beauvericin (BEA) is a cyclic hexadepsipeptide, which derives from Cordyceps cicadae. It is also produced by Fusarium species, which are parasitic to maize, wheat, rice and other important commodities. BEA increases ion permeability in biological membranes by forming a complex with essential cations, which may affect ionic homeostasis. Its ion-complexing capability allows BEA to transport alkaline earth metal and alkali metal ions across cell membranes. Importantly, increasing lines of evidence show that BEA has an anticancer effect and can be potentially used in cancer therapeutics. Normally, BEA performs the anticancer effect due to the induced cancer cell apoptosis via a reactive oxygen species-dependent pathway. Moreover, BEA increases the intracellular Ca2+ levels and subsequently regulates the activity of a series of signalling pathways including MAPK, JAK/STAT, and NF-κB, and finally causes cancer cell apoptosis. In vivo studies further show that BEA reduces tumour volumes and weights. BEA especially targets differentiated and invasive cancer types. Currently, the anticancer activity of BEA is a hot topic; however, there is no review article to discuss the anticancer activity of BEA. Therefore, in this review, we have mainly summarized the anticancer activity of BEA and thoroughly discussed its underlying mechanisms. In addition, the human exposure risk assessment of BEA is also discussed. We hope that this review will provide further information for understanding the anticancer mechanisms of BEA.


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