US2004259126A1PendingUtilityA1

MN gene and protein

Priority: Mar 11, 1992Filed: Mar 8, 2004Published: Dec 23, 2004
Est. expiryMar 11, 2012(expired)· nominal 20-yr term from priority
C12N 9/88A61P 35/00C07K 16/3069C07K 2317/34C07K 7/06C07K 16/32C07K 16/08C07K 14/82A61K 38/00C07K 2319/00A61K 39/00
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Claims

Abstract

A new gene—MN—and proteins/polypeptides encoded therefrom are disclosed. Recombinant nucleic acid molecules for expressing MN proteins/polypeptides and recombinant proteins are provided. Expression of the MN gene is disclosed as being associated with tumorigenicity, and the invention concerns methods and compositions for detecting and/or quantitating MN antigen and/or MN-specific antibodies in vertebrate samples that are diagnostic/prognostic for neoplastic and pre-neoplastic disease. Test kits embodying the immunoassays of this invention are provided. MN-specific antibodies are disclosed that can be used diagnostically/prognostically, therapeutically, for imaging, and/or for affinity purification of MN proteins/polypeptides. Also provided are nucleic acid probes for the MN gene as well as test kits comprising said probes. The invention also concerns vaccines comprising MN proteins/polypeptides which are effective to immunize a vertebrate against neoplastic diseases associated with the expression of MN proteins. The invention still further concerns antisense nucleic acid sequences that can be used to inhibit MN gene expression.

Claims

exact text as granted — not AI-modified
1 - 30  (canceled).  
     
     
         31 . An MN antisense construct comprising an MN antisense oligonucleotide operably linked to an expression control sequence in a vector, wherein said MN antisense oligonucleotide is complementary to SEQ ID NO: 5, and wherein said MN antisense construct shows antisense activity in an in vitro screening assay comprising the steps of: 
 (a) contacting a human cell abnormally expressing MN with said MN antisense construct;    (b) determining the effect of said MN antisense construct on MN expression in said human cell; and    (c) concluding that if MN expression is decreased, that said MN antisense construct shows antisense activity.    
     
     
         32 . The MN antisense construct of  claim 31 , wherein said MN antisense nucleotide is complementary to the 5′ end of the mRNA that is transcribed from the complement of SEQ ID NO: 5.  
     
     
         33 . The MN antisense construct of  claim 31 , wherein said MN antisense nucleotide is complementary to SEQ ID NO: 1.  
     
     
         34 . The MN antisense construct of  claim 31 , wherein said vector is derived from a plasmid, a cosmid, a bacteriophage or a virus.  
     
     
         35 . A composition comprising a pharmaceutically acceptable carrier and the MN antisense construct of  claim 31 , wherein said MN antisense construct interacts with MN gene or MN transcript.  
     
     
         36 . An MN antisense construct comprising an MN antisense double-stranded ribonucleic acid operably linked to an expression control sequence in a vector, wherein said MN antisense double-stranded ribonucleic acid consists of a nucleotide sequence that is complementary to SEQ ID NO: 5, and wherein said MN antisense double-stranded ribonucleic acid shows antisense activity in an in vitro screening assay comprising the steps of: 
 (a) contacting a human cell abnormally expressing MN with said MN antisense double-stranded ribonucleic acid;    (b) determining the effect of said MN antisense double-stranded ribonucleic acid on MN expression in said human cell; and    (c) concluding that if MN expression is decreased, that said MN antisense double-stranded ribonucleic acid shows antisense activity.    
     
     
         37 . The MN antisense construct of  claim 36 , wherein said vector is derived from a plasmid, a cosmid, a bacteriophage or a virus.  
     
     
         38 . A composition comprising a pharmaceutically acceptable carrier and the MN antisense construct according to  claim 36 , wherein said MN antisense construct interacts with MN gene or MN transcript.  
     
     
         39 . A method of blocking in vivo expression of the MN gene in a human by administering an MN antisense construct of  claim 31 .  
     
     
         40 . A method of treating neoplastic disease and/or pre-neoplastic disease in a human, wherein said disease is associated with abnormal MN gene expression, comprising inhibiting the expression of MN gene by administering an MN antisense construct according to  claim 31 .  
     
     
         41 . An antibody which specifically binds to an MN protein or to an MN polypeptide, wherein said MN protein or MN polypeptide is encoded by a nucleic acid that comprises a polynucleotide containing at least 29 nucleotides, said nucleic acid being selected from the group consisting of: 
 (a) SEQ ID NO: 5;    (b) polynucleotides that hybridize under stringent conditions to SEQ ID NO: 5's complement; and    (c) polynucleotides that differ from SEQ ID NO: 5 or from the polynucleotide sequences of (b) due to the degeneracy of the genetic code,    and wherein said antibody is polyclonal.    
     
     
         42 . The antibody of  claim 41  that is conjugated to a toxin.  
     
     
         43 . The antibody of  claim 41  that is conjugated to a chemotherapeutic drug.  
     
     
         44 . An antibody which specifically binds to an MN protein or to an MN polypeptide, wherein said MN protein or MN polypeptide is encoded by a nucleic acid that comprises a polynucleotide containing at least 29 nucleotides, said nucleic acid being selected from the group consisting of: 
 (a) SEQ ID NO: 5;    (b) polynucleotides that hybridize under stringent conditions to SEQ ID NO: 5's complement; and    (c) polynucleotides that differ from SEQ ID NO: 5 or from the polynucleotide sequences of (b) due to the degeneracy of the genetic code,    and wherein said antibody is humanized.    
     
     
         45 . The antibody of  claim 44  that is conjugated to a toxin.  
     
     
         46 . The antibody of  claim 44  that is conjugated to a chemotherapeutic drug.

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