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Advisor(s)
Abstract(s)
Mushrooms are a vast and yet largely untapped source of powerful new pharmaceutical
products. In particular, and most importantly for modern medicine, they represent an
unlimited source of compounds with antitumor and immunostimulating properties [1].
Particularly, the intake of some wild mushrooms has shown to reduce the risk of breast
cancer in Chinese women [2]. A large number of LMW (low molecular weight)
compounds have been "identified in wild mushrooms including phenolic acids,
flavonoids, tocopherols, carotenoids, sugars and fatty acids [3]. In this study we used
AutoDock 4 [4] to perform virtual ligand screening in order to evaluate which LMW
compounds may be involved in the inhibition of the activity of proteins related to
human breast cancer: aromatase (EC: 1.14.14.1), estrone sulfatase (EC: 3.1.6.2) and 17-
hydroxysteroid dehydrogenase type 1 activity (17~-HSD-1; EC:. 1.1.1.62) [5]. A
representative dataset of 43 LMW compounds was selected and molecular docking was
performed against the three protein targets. 4-0-caffeoylquinic, naringin and lycopene stand out as the top ranked potential inhibitors for aromatase, estrone sulfatase and 1 7~HSD1,
respectively. The information provided shows several interesting starting points
for further development of inhibitors of the studied proteins, as also for the development of nutraceuticals or functional foods.
Description
Keywords
Citation
Froufe, Hugo J.C.; Abreu, Rui M.V.; Ferreira, Isabel C.F.R. (2010). Virtual ligand screening studies between mushroom compounds and proteins involved in breast cancer. In IV Jornadas de Análises Clínicas e Saúde Pública de Bragança