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Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity

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Journal PLoS One
Date 2009 Dec 4
PMID 19956630
Citations 12
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Abstract

Immunohistochemistry is one of the most suitable methods for the detection of intratumoral aromatase in order to identify patients who may respond to aromatase inhibitor therapy in hormone-dependent breast cancer. Previous studies showed statistically significant correlation between results of immnuohistochemistry and biochemical analysis in carcinoma components stained by aromatase monoclonal antibody 677. In this study, determination of the antigenic peptides recognized by aromatase antibodies through epitope mapping, combined with the new knowledge on aromatase-reductase interaction, provide insights for understanding various immunostaining patterns using different aromatase antibodies. Our studies on aromatase-reductase interaction also provided critical information on how aromatase and reductase interact with each other on the endoplasmic reticulum membrane, and identified key residues, including K108 of aromatase, that are involved in the interaction with reductase. Through epitope mapping and taking into consideration the interference with aromatase immunohistochemical staining by NADPH-cytochrome P450 reductase, we demonstrated that monoclonal antibody 677 is a suitable antibody for an assessment of intratumoral aromatase activity in breast cancer patients for making clinical management decisions. These results also provide valuable information to identify new aromatase antibodies for immunohistochemical diagnosis of hormone-dependent breast cancer in future.

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References
1.
Lu Q, Nakmura J, Savinov A, Yue W, Weisz J, Dabbs D . Expression of aromatase protein and messenger ribonucleic acid in tumor epithelial cells and evidence of functional significance of locally produced estrogen in human breast cancers. Endocrinology. 1996; 137(7):3061-8. DOI: 10.1210/endo.137.7.8770932. View

2.
Sasano H, Anderson T, Silverberg S, Santen R, Conway M, Edwards D . The validation of new aromatase monoclonal antibodies for immunohistochemistry--a correlation with biochemical activities in 46 cases of breast cancer. J Steroid Biochem Mol Biol. 2005; 95(1-5):35-9. DOI: 10.1016/j.jsbmb.2005.04.027. View

3.
Bernhardt R, Pommerening K, Ruckpaul K . Modification of carboxyl groups on NADPH-cytochrome P-450 reductase involved in binding of cytochromes c and P-450 LM2. Biochem Int. 1987; 14(5):823-32. View

4.
Nelson D, Strobel H . On the membrane topology of vertebrate cytochrome P-450 proteins. J Biol Chem. 1988; 263(13):6038-50. View

5.
Shimizu T, Tateishi T, Hatano M, Fujii-Kuriyama Y . Probing the role of lysines and arginines in the catalytic function of cytochrome P450d by site-directed mutagenesis. Interaction with NADPH-cytochrome P450 reductase. J Biol Chem. 1991; 266(6):3372-5. View