US2005026158A1PendingUtilityA1

Methods of diagnosing and treating hepatic cell proliferative disorders

Assignee: UNIV JOHNS HOPKINS MEDPriority: Oct 13, 1999Filed: Sep 15, 2003Published: Feb 3, 2005
Est. expiryOct 13, 2019(expired)· nominal 20-yr term from priority
G01N 33/573C12Q 1/6886C12Q 2521/331C12Q 2523/125C12Q 2600/106C12Q 2600/154G01N 33/576G01N 2333/91171
42
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Claims

Abstract

Provided are methods and compositions useful for the diagnosis, prognosis and treatment of hepatic cellular proliferative disorders. The methods include the modulation or analysis of hypemethylated glutathione-S-transferase nuleic acid sequence in hepatic samples and biological fluids.

Claims

exact text as granted — not AI-modified
1 - 75 . (canceled).  
     
     
         76 . A kit useful for the detection of a methylated CpG-containing nucleic acid in a GSTP1 promoter comprising carrier means containing one or more containers comprising a first container containing a reagent which modifies unmethylated cytosine and a second container containing primers for amplification of the CpG-containing nucleic acid, wherein the primers distinguish between modified methylated and nonmethylated nucleic acid.  
     
     
         77 . The kit of  claim 76 , wherein the modifying regent is bisulfite.  
     
     
         78 . The kit of  claim 76 , wherein said reagent modifies cytosine to uracil.  
     
     
         79 . The kit of  claim 76 , wherein the primer hybridizes with a target polynucleotide sequence having the sequence from about −539 to −239 upstream from GSTP1 transcription start site.  
     
     
         80 . The kit of  claim 79 , wherein the primers are SEQ ID Nos: 1, 2, 7, 8, 9, 10, 11, 12, or 13 or any combination thereof.  
     
     
         81 . The kit of  claim 76 , further comprising nucleic acid amplification buffer.  
     
     
         82 . Isolated oligonucleotide primer(s) for detection of a methylated CpG-containing nucleic acid wherein the primer hybridizes with a target polynucleotide sequence having the sequence in the region from about −539 to −239 upstream from GSTP1 transcription start site.  
     
     
         83 . The primers of  claim 81 , wherein the primers are SEQ ID Nos: 1, 2, 7, 8, 9, 10, 11, 12, or 13 or any combination thereof.  
     
     
         84 - 85 . (canceled).

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