Method of analysing a blood sample of a subject for the presence of a disease marker
The present invention relates to a method of analyzing a blood sample of a subject for the presence of a disease marker, said method comprising the steps of a) extracting nucleic acid from anucleated blood cells in said blood sample to provide an anucleated blood cells-extracted nucleic acid fraction, and b) analyzing said anucleated blood cells-extracted nucleic acid fraction for the presence of a disease marker, wherein said disease marker is a disease-specific mutation in a gene of a cell of said subject, or wherein said disease marker is a disease-specific expression profile of genes of a cell of said subject.
1. A method of quantifying RNA levels in a blood sample of a subject, said method comprising the steps of:
a) isolating thrombocytes from the blood sample;
b) extracting messenger ribonucleic acid (mRNA) from said thrombocytes to provide an extracted nucleic acid fraction from said thrombocytes;
c) analyzing said extracted nucleic acid fraction by reverse transcribing extracted mRNA into cDNA, quantifying said cDNA to determine the amount of mRNA of at least three genes by conducting an amplification reaction which employs gene specific primers, wherein the at least three genes comprise genes encoding prostate cancer antigen 3, prostate-specific antigen, and epidermal growth factor receptor variant III.
2. The method of claim 1 , wherein the primers for prostate specific antigen comprise SEQ ID NO: 3 and SEQ ID NO: 4.
3. The method of claim 1 , wherein the primers for prostate cancer antigen 3 comprise SEQ ID NO: 5 and SEQ ID NO: 6.
4. The method of claim 1 , wherein the primers for prostate cancer antigen 3 comprise SEQ ID NO: 7 and SEQ ID NO: 8.
5. The method of claim 1 , wherein the primers for epidermal growth factor receptor variant III comprise SEQ ID NO: 9 and SEQ ID NO: 10.
6. The method of claim 1 , wherein the primers for epidermal growth factor receptor variant III comprise SEQ ID NO: 11 and SEQ ID NO: 12.