Method to detect prostate cancer in a sample
The present invention provides methods to detect prostate cancer by detecting the RNA encoded by PCA3. The disclosure provides a method for determining a predisposition, or presence of prostate cancer comprising: (a) contacting a sample with at least one oligonucleotide that hybridizes to a PCA3 polynucleotide; (b) detecting an amount of PCA3 and second prostate-specific polynucleotides; and (c) comparing the amount of PCA3 polynucleotide that hybridizes to the oligonucleotide to a predetermined cut off value, and determining the presence or absence of prostate cancer. Diagnostic kits are provided for detecting prostate cancer or the risk of developing same comprising: (a) at least one container means containing at least one oligonucleotide probe or primer that hybridizes to PCA3 (b) at least one oligonucleotide probe or primer that hybridizes with a second prostate specific nucleic acid; and (c) reagents for detecting PCA3 and the second prostate specific nucleic acid.
1. A method of characterizing nucleic acids of a urine sample, the method comprising:
(a) performing a first amplification reaction on nucleic acids of the urine sample using at least a first primer pair to produce a first amplification product, wherein:
the first primer pair is specific for a PCA3 RNA or a cDNA prepared therefrom,
the urine sample comprises at least one prostate cell or nucleic acid extract thereof, and
the PCA3 RNA:
(i) comprises the sequence of SEQ ID NO: 9, 10 or 13,
(ii) hybridizes under high stringency conditions to the RNA of (i), wherein the high stringency conditions comprise a hybridization at 65° C. in 6×SSC or 5×SSPE, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured carrier DNA and a washing at 65° C. in 0.2×SSC/0.1% SDS, or
(iii) is fully complementary to the RNA of (i) or (ii);
(b) performing a second amplification reaction on nucleic acids of the urine sample using at least a second primer pair to produce a second amplification product, wherein the second primer pair is specific for a PSA RNA or a cDNA prepared therefrom; and
(c) detecting levels of the first and the second amplification products produced in the first and second amplification reactions, respectively.
2. The method of claim 1 , wherein the urine sample comprises malignant prostate cells or a nucleic acid extract thereof.
3. The method of claim 1 , wherein the urine sample comprises crude urine.
4. The method of claim 1 , wherein the urine sample comprises the first voided urine following a digital rectal examination.
5. The method of claim 1 , comprising simultaneously amplifying the PCA3 RNA or cDNA prepared therefrom and the PSA RNA or cDNA prepared therefrom to produce the first and second amplification products, respectively, in a multiplex reaction.
6. The method of claim 1 , comprising performing a nucleic acid amplification which is at least one of:
(a) real-time amplification;
(b) nucleic acid sequence-based amplification (NASBA);
(c) polymerase chain reaction (PCR);
(d) transcription-mediated amplification assay (TMA); or
(e) ligase chain reaction.
7. The method of claim 1 , comprising detecting levels of the first and second amplification products using fluorescence detection, chemiluminescence detection, or colorimetry detection.
8. The method of claim 1 , wherein the first primer pair comprises a promoter-primer suitable for transcription-mediated amplification of the PCA3 RNA or cDNA prepared therefrom.
9. The method of claim 1 , wherein the urine sample comprises RNA extracted from crude urine using:
(a) a silica based purification method, or
(b) a target capture method.
10. The method of claim 1 , wherein the first amplification product comprises PCA3 exon sequences or the complements thereof, but does not comprise PCA3 intron sequences.
11. The method of claim 10 , wherein the first primer pair amplifies sequences from PCA3 exon 3 and exon 4 without amplifying any sequence from an intron therebetween.
12. The method of claim 1 , wherein the first amplification reaction is a first isothermal amplification reaction that cannot use genomic DNA as a template to produce the first amplification product.
13. The method of claim 12 , wherein the first primer pair amplifies sequences from PCA3 exon 3 and exon 4 without amplifying any sequence from an intron therebetween.
14. The method of claim 13 , wherein steps (a) and (c) are carried out simultaneously in a multiplex reaction.
15. The method of claim 14 , wherein the urine sample comprises the first voided urine following a digital rectal examination.
16. The method of claim 15 , wherein the urine sample comprises malignant prostate cells or a nucleic acid extract thereof.
17. The method of claim 14 , wherein step (c) comprises detecting the level of the first amplification product with a first hybridization probe, and detecting the level of the second amplification product with a second hybridization probe, wherein each of the hybridization probes comprises a different fluorophore.
18. The method of claim 1 , wherein steps (a) and (c) are carried out simultaneously in a multiplex reaction, and wherein the first and second amplification reactions of the multiplex reaction are first and second transcription mediated amplification reactions.
19. The method of claim 1 , wherein the first primer pair comprises oligonucleotides comprising the sequences set forth in SEQ ID NOs: 3 and 4.
20. The method of claim 1 , wherein the second primer pair comprises oligonucleotides comprising the sequence set forth in SEQ ID NOs: 1 and 2.