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[Cancer Research 49, 2379-2382, May 1, 1989]
© 1989 American Association for Cancer Research

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Molecular Characterization of the Epitope in Prostate and Breast Tumor-associated PR92 Antigen

Yung D. Kim1, Deborah Y. Robinson, George L. Manderino, Ilse I. E. Tribby and Joseph T. Tomita

Diagnostics Division, D90C, Abbott Laboratories, North Chicago, Illinois 60064

In our previous report, monoclonal antibody PR92 has defined prostate- and breast tumor-associated PR92 antigen. The molecular nature of PR92 antigen, especially the epitope involved in specific interaction with PR92 monoclonal antibody, is described. PR92 antigen was purified from the cell extract or tissue culture medium of prostate cancer cell line DU145 by means of monoclonal antibody-coupled Sepharose 4B affinity chromatography, followed by a Sephacryl S-500 chromatography. Physical and chemical characterization, coupled with high-performance liquid chromatography, determined that PR92 antigen is a glycoprotein with a molecular weight of about 470,000, comprising repeating subunits of about 44,000. Sialic acid was found to form a critical part, while D-galactose and N-acetylgalactosamine were also involved, in the epitope structure. PR92 antigen is rich in serine, threonine, proline, glycine, and alanine and poor in aromatic amino acid residues. The carbohydrate moieties may be predominantly O-linked to polypeptide chains which contribute directly or indirectly to maintain the integrity of the epitope. Elucidation of the molecular nature of PR92 antigen may help understand the mechanism of shedding into the body fluids during tumor progression.

1 To whom requests for reprints should be addressed.

Received 7/13/88. Revised 10/21/88. Accepted 1/25/89.




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J. Xu, J. A. Stolk, X. Zhang, S. J. Silva, R. L. Houghton, M. Matsumura, T. S. Vedvick, K. B. Leslie, R. Badaro, and S. G. Reed
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[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 1989 by the American Association for Cancer Research.