Gene differentially expressed in breast and bladder cancer,...

Chemistry: natural resins or derivatives; peptides or proteins; – Peptides of 3 to 100 amino acid residues

Reexamination Certificate

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C530S350000, C424S184100, C424S185100

Reexamination Certificate

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09824787

ABSTRACT:
The present invention relates to a novel human gene that is differentially expressed in human carcinoma. More specifically, the present invention relates to a polynucleotide encoding a novel human polypeptide named C35 that is overexpressed in human breast and bladder carcinoma. This invention also relates to C35 polypeptides, as well as vectors, host cells, antibodies directed to C35 polypeptides, and the recombinant methods for producing the same. The present invention further relates to diagnostic methods for detecting carcinomas, including human breast carcinomas. The present invention further relates to the formulation and use of the C35 gene and polypeptides in immunogenic compositions or vaccines, to induce antibody or cell-mediated immunity against target cells, such as tumor cells, that express the C35 gene. The invention further relates to screening methods for identifying agonists and antagonists of C35 activity.

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GenCore database, amino acid sequence comparison between Applicants' SEQ ID No. 2 and sequence 3 of U.S. Patent No. 5,856,131, Jan. 5, 1999.
Lazar et al. Molecular and Cellular Biology 8(3): 1247-1252, Mar. 1988.
GenCore database sheet (1). Amino acid alignment between Applicants' SEQ ID No. 2 and U.S. Patent application publication's sequence No. 966. May 2, 2002.
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Del Val, M., et al., “Efficient Processing of an Antigenic Sequence for Presentation by MHC Class I Molecules Depends on Its Neighboring Residues in the Protein,”Cell66:1145-1153, Cell Press (1991).
Eisenlohr, L.C., et al., “Flanking Sequences Influence the Presentation of an Endogenously Synthesized Peptide to Cytotoxic T Lymphocytes,”J. Exp. Med.175:481-487, Rockefeller University Press (1992).
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