Method for discriminating between prostatic cancer and...

Chemistry: analytical and immunological testing – Peptide – protein or amino acid – Glycoproteins

Reexamination Certificate

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C436S064000, C436S086000, C436S171000

Reexamination Certificate

active

08030085

ABSTRACT:
The present invention provides a method for accurately discriminating between prostate carcinoma and benign prostatic hyperplasia based on a glycan structure of prostate specific antigen (PSA). The method of the present invention includes the steps of: purifying PSA from a sample derived from a subject; preparing a PSA derivative from the PSA; labeling the PSA derivative; and analyzing the labeled PSA derivative by the mass spectrometry method, in which the subject is identified as having prostate carcinoma when the ratio of the signal intensity of fucose-unbound glycan to the signal intensity of fucose-bound glycan in the labeled PSA derivative is greater than 1.0, and identified as having benign prostatic hyperplasia when the ratio is 1.0 or less.

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Jun. 9, 2010 European Search Report issued in EP 08 77 7915.

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