US2010190176A1PendingUtilityA1

Tumor suppressor designated ts10q23.3

Assignee: UNIV TEXASPriority: Jan 30, 1997Filed: Apr 1, 2010Published: Jul 29, 2010
Est. expiryJan 30, 2017(expired)· nominal 20-yr term from priority
G01N 33/57557G01N 33/57555G01N 33/57595C07K 14/4703G01N 2333/916C12Q 2600/172C12N 9/16C12Q 2600/16C12Q 2600/136C12Q 2600/112A01K 2217/075C12Q 1/6886C12N 2799/021A61K 48/00A61K 38/00
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Claims

Abstract

A specific region of chromosome 10 (10q23.3) has been implicated by series of studies to contain a tumor suppressor gene involved in gliomas, as well as a number of other human cancers. One gene within this region was identified, and the corresponding coding region of the gene represents a novel 47 kD protein. A domain of this product has an exact match to the conserved catalytic domain of protein tyrosine phosphatases, indicating a possible functional role in phosphorylation events. Sequence analyses demonstrated the a number of exons of the gene were deleted in tumor cell lines used to define the 10q23.3 region, leading to the classification of this gene as a tumor suppressor. Further analyses have demonstrated the presence of a number of mutations in the gene in both glioma and prostate carcinoma cells. Methods for diagnosing and treating cancers related to this tumor suppressor, designated as TS10q23.3, also are disclosed.

Claims

exact text as granted — not AI-modified
1 . An isolated nucleic acid or the complement thereof, wherein said nucleic acid comprises a nucleic acid sequence having 16 or more nucleotides of SEQ ID NO:1 (cDNA). 
     
     
         2 . A method of amplifying a PTEN nucleic acid comprising contacting a patient sample with an oligonucleotide primer specific for PTEN under conditions and together with reagents suitable for amplification. 
     
     
         3 . The method of  claim 2 , wherein said oligonucleotide primer comprises at least 15 consecutive nucleotides of any one of SEQ ID NOs 1 or 8-16. 
     
     
         4 . A method of detecting a PTEN nucleic acid comprising contacting a patient sample with an oligonucleotide probe specific for PTEN under conditions and together with reagents suitable for detection.

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