The structural biology of oestrogen metabolism

作者: Mark P. Thomas , Barry V.L. Potter

DOI: 10.1016/J.JSBMB.2012.12.014

关键词:

摘要: Many enzymes catalyse reactions that have an oestrogen as a substrate and/or product. The catalysed include aromatisation, oxidation, reduction, sulfonation, desulfonation, hydroxylation and methoxylation. these must all recognise bind but, despite this, they diverse structures. This review looks at each of in turn, describing the structure discussing mechanism reaction. Since has role many disease states inhibition metabolism may impact on state or progression inhibitors are briefly discussed. article is part Special Issue entitled 'CSR 2013'.

参考文章(152)
David A. Learmonth, László E. Kiss, Patrício Soares-da-Silva, The chemistry of catechol-O-methyltransferase inhibitors. International Review of Neurobiology. ,vol. 95, pp. 119- 162 ,(2010) , 10.1016/B978-0-12-381326-8.00006-5
George Betz, Reaction Mechanism of 17β-Estradiol Dehydrogenase Determined by Equilibrium Rate Exchange Journal of Biological Chemistry. ,vol. 246, pp. 2063- 2068 ,(1971) , 10.1016/S0021-9258(19)77189-0
Erkki Nissinen, Pekka T. Männistö, Biochemistry and Pharmacology of Catechol-O-Methyltransferase Inhibitors International Review of Neurobiology. ,vol. 95, pp. 73- 118 ,(2010) , 10.1016/B978-0-12-381326-8.00005-3
A. A. J. van Landeghem, J. H. H. Thijssen, M. Nabuurs, J. Poortman, Endogenous Concentration and Subcellular Distribution of Estrogens in Normal and Malignant Human Breast Tissue Cancer Research. ,vol. 45, pp. 2907- 2912 ,(1985)
R.W. Woodard, M.D. Tsai, H.G. Floss, P.A. Crooks, J.K. Coward, Stereochemical course of the transmethylation catalyzed by catechol O-methyltransferase. Journal of Biological Chemistry. ,vol. 255, pp. 9124- 9127 ,(1980) , 10.1016/S0021-9258(19)70536-5
Mariam M. AlHilli, Harry J. Long, Karl C. Podratz, Jamie N. Bakkum-Gamez, Aromatase inhibitors in the treatment of recurrent ovarian granulosa cell tumors: brief report and review of the literature. Journal of Obstetrics and Gynaecology Research. ,vol. 38, pp. 340- 344 ,(2012) , 10.1111/J.1447-0756.2011.01698.X
C. Mazza, R. Breton, D. Housset, J.-C. Fontecilla-Camps, Human Type I 17Beta-Hydroxysteroid Dehydrogenase: Site Directed Mutagenesis and X-Ray Crystallography Structure-Function Analysis Thesis, Universite Joseph Fourier. ,(1998) , 10.2210/PDB1A27/PDB
O Shimozawa, M Sakaguchi, H Ogawa, N Harada, K Mihara, T Omura, Core glycosylation of cytochrome P-450(arom). Evidence for localization of N terminus of microsomal cytochrome P-450 in the lumen. Journal of Biological Chemistry. ,vol. 268, pp. 21399- 21402 ,(1993) , 10.1016/S0021-9258(19)36937-6
C Stein, A Hille, J Seidel, S Rijnbout, A Waheed, B Schmidt, H Geuze, K von Figura, Cloning and expression of human steroid-sulfatase. Membrane topology, glycosylation, and subcellular distribution in BHK-21 cells. Journal of Biological Chemistry. ,vol. 264, pp. 13865- 13872 ,(1989) , 10.1016/S0021-9258(18)80080-1
Muhammad Akhtar, Michael R. Calder, David L. Corina, J. Neville Wright, Mechanistic studies on C-19 demethylation in oestrogen biosynthesis. Biochemical Journal. ,vol. 201, pp. 569- 580 ,(1982) , 10.1042/BJ2010569