US2020095642A1PendingUtilityA1

Grading of breast cancer

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Assignee: BIOTHERANOSTICS INCPriority: Dec 21, 2001Filed: May 6, 2019Published: Mar 26, 2020
Est. expiryDec 21, 2021(expired)· nominal 20-yr term from priority
A61K 31/138C12Q 2600/158C12Q 2600/112C12Q 2600/16C12Q 1/6886G01N 33/57595G01N 33/57515G01N 33/57496G01N 33/57415
74
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Claims

Abstract

Methods and compositions for the identification of breast cancer grade signatures are provided. The signature profiles are identified based upon multiple sampling of reference breast tissue samples from independent cases of breast cancer and provide a reliable set of molecular criteria for identification of cells as being in one or more particular stages and/or grades of breast cancer.

Claims

exact text as granted — not AI-modified
1 . A method to determine the grade of breast cancer cells in a sample from a human subject, said method comprising
 assaying said sample for gene expression that is increased in a high proliferation index of grade III relative to grade I breast cancer, wherein said gene expression is assayed by synthesis of cDNA.   
     
     
         2 . The method of  claim 1 , wherein the gene expression is assayed by synthesis of cDNA from expressed RNA of the gene CENPA (centromere protein A (17 kD), chromosomal location 2p24-p21). 
     
     
         3 . A method to determine the grade of breast cancer cells in a sample from a human subject, said method comprising
 assaying said sample for gene expression that is increased in grade III relative to grade I breast cancer, wherein said gene expression is assayed by synthesis of cDNA from expressed RNA of a gene selected from   RACGAP1 (Rac GTPase activating protein 1, chromosomal location 12p13.2-p13.1),   RRM2 (ribonucleotide reductase M2 polypeptide, chromosomal location 2p25-p24), and   NEK2 (NIMA (never in mitosis gene a)-related kinase, chromosomal location Iq32.2-q41)   in the sample; and   comparing the expression of the genes, via the cDNA molecules, to the expression of said genes in reference samples of known human grade III breast cancer; and   identifying said sample as containing grade III breast cancer cells.   
     
     
         4 . The method of  claim 1  wherein said assaying comprises preparing RNA from said sample. 
     
     
         5 . The method of  claim 4  wherein said RNA is amplified by quantitative PCR to produce cDNA. 
     
     
         6 . The method of  claim 4  wherein said RNA is amplified by reverse transcription PCR (RT-PCR) to produce cDNA. 
     
     
         7 . The method of  claim 1  wherein said assaying comprises determining gene expression by an array. 
     
     
         8 . The method of  claim 1  wherein said sample is a ductal lavage or fine needle aspirate sample. 
     
     
         9 . The method of  claim 7  wherein said sample is microdissected to isolate one or more cells suspected of being breast cancer cells and said assaying is of RNA in said isolated cells. 
     
     
         10 . A method to determine the grade of breast cancer cells in a sample from a human subject, said method comprising
 assaying said sample for gene expression that is decreased in a high proliferation index of grade III relative to grade I breast cancer, wherein said gene expression is assayed by synthesis of cDNA molecules.   
     
     
         11 . The method of  claim 10  wherein said assaying comprises preparing RNA from said sample. 
     
     
         12 . The method of  claim 11  wherein said RNA is amplified by quantitative PCR to produce cDNA molecules. 
     
     
         13 . The method of  claim 11  wherein said RNA is amplified by reverse transcription PCR (RT-PCR) to produce cDNA molecules. 
     
     
         14 . The method of  claim 10  wherein said assaying comprises determining gene expression by an array. 
     
     
         15 . The method of  claim 10  wherein said sample is a ductal lavage or fine needle aspirate sample. 
     
     
         16 . The method of  claim 15  wherein said sample is microdissected to isolate one or more cells suspected of being breast cancer cells and said assaying is of RNA in said isolated cells.

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