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1.
Int J Toxicol ; 43(3): 253-290, 2024.
Article in English | MEDLINE | ID: mdl-38204208

ABSTRACT

The ten key characteristics (KCs) of carcinogens are based on characteristics of known human carcinogens and encompass many types of endpoints. We propose that an objective review of the large amount of cancer mechanistic evidence for the chemical bisphenol A (BPA) can be achieved through use of these KCs. A search on metabolic and mechanistic data relevant to the carcinogenicity of BPA was conducted and web-based software tools were used to screen and organize the results. We applied the KCs to systematically identify, organize, and summarize mechanistic information for BPA, and to bring relevant carcinogenic mechanisms into focus. For some KCs with very large data sets, we utilized reviews focused on specific endpoints. Over 3000 studies for BPA from various data streams (exposed humans, animals, in vitro and cell-free systems) were identified. Mechanistic data relevant to each of the ten KCs were identified, with receptor-mediated effects, epigenetic alterations, oxidative stress, and cell proliferation being especially data rich. Reactive and bioactive metabolites are also associated with a number of KCs. This review demonstrates how the KCs can be applied to evaluate mechanistic data, especially for data-rich chemicals. While individual entities may have different approaches for the incorporation of mechanistic data in cancer hazard identification, the KCs provide a practical framework for conducting an objective examination of the available mechanistic data without a priori assumptions on mode of action. This analysis of the mechanistic data available for BPA suggests multiple and inter-connected mechanisms through which this chemical can act.


Subject(s)
Benzhydryl Compounds , Carcinogens , Phenols , Phenols/toxicity , Benzhydryl Compounds/toxicity , Humans , Animals , Carcinogens/toxicity , Neoplasms/chemically induced
2.
J Agric Food Chem ; 60(36): 8924-9, 2012 Sep 12.
Article in English | MEDLINE | ID: mdl-22697360

ABSTRACT

This study evaluated the inhibitory effects of plant-based extracts (grape seed, green tea, and white tea) and their constituent flavan-3-ol monomers (catechins) on α-amylase and α-glucosidase activity, two key glucosidases required for starch digestion in humans. To evaluate the relative potency of extracts and catechins, their concentrations required for 50 and 90% inhibition of enzyme activity were determined and compared to the widely used pharmacological glucosidase inhibitor, acarbose. Maximum enzyme inhibition was used to assess relative inhibitory efficacy. Results showed that grape seed extract strongly inhibited both α-amylase and α-glucosidase activity, with equal and much higher potency, respectively, than acarbose. Whereas tea extracts and catechin 3-gallates were less effective inhibitors of α-amylase, they were potent inhibitors of α-glucosidase. Nongallated catechins were ineffective. The data show that plant extracts containing catechin 3-gallates, in particular epigallocatechin gallate, are potent inhibitors of α-glucosidase activity and suggest that procyanidins in grape seed extract strongly inhibit α-amylase activity.


Subject(s)
Camellia sinensis/chemistry , Catechin/analogs & derivatives , Enzyme Inhibitors/pharmacology , Glycoside Hydrolase Inhibitors , Plant Extracts/pharmacology , Vitis/chemistry , alpha-Amylases/antagonists & inhibitors , Catechin/pharmacology , Fungal Proteins/antagonists & inhibitors , Fungal Proteins/chemistry , Humans , Kinetics , Saccharomycetales/enzymology , Saliva/enzymology , Seeds/chemistry , alpha-Amylases/chemistry , alpha-Glucosidases/chemistry
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