Detection of survivin in the biological fluids of cancer patients
The present invention includes a method for diagnosing cancer comprising detecting the presence of survivin in the biological fluid of a patient. The present invention also provides kits comprising one or more agents that detect survivin polypeptide or survivin nucleic acid and a container for collecting biological fluid for testing.
1. A method of diagnosing cancer in a patient comprising assaying a sample of urine supernatant from a patient for the presence or absence of survivin, wherein the presence of survivin in the sample indicates that the patient has cancer.
2. The method of claim 1 , wherein the cancer is a cancer invading the genitourinary tract.
3. The method for claim 2 , wherein the genitourinary tract cancer is bladder or prostate cancer.
4. The method of claim 3 , wherein the bladder or prostate cancer is graded as a CIS (Carcinoma in situ).
5. The method of claim 3 , wherein the bladder or prostate cancer is any grade or any stage.
6. The method of claim 1 , wherein survivin is detected using an agent selected from the group consisting of antibodies that bind survivin, survivin binding partners, and nucleic acids that hybridize to a nucleic acid encoding survivin.
7. The method of claim 6 , wherein the agent is tagged with a label.
8. The method of claim 7 , wherein the label is a radioactive label, a fluorescent label, an enzyme, or a chemiluminescent tag.
9. The method of claim 1 , wherein survivin is detected by an immunoassay.
10. The method of claim 9 , wherein the immunoassay is an enzyme linked immunosorbent assay or radioimmunoassay.
11. The method of claim 9 , wherein the immunoassay comprises immunoblotting, immunodiffusion, immunoelectrophoresis, or immunoprecipitation.
12. The method of claim 1 , wherein survivin is detected by dot blotting.
13. The method of claim 12 , wherein dot blotting comprises using a Bio-Dot SF module.
14. The method of claim 1 , wherein survivin is detected by nucleic acid hybridization.
15. The method of claim 14 , wherein the nucleic acid hybridization is RT-PCR or Northern blot analysis.
16. A kit for the diagnosis, prognosis, or monitoring of cancer, comprising a container for collecting urine supernatant from a patient and an agent that detects the presence of survivin in the urine supernatant.
17. The kit of claim 16 , wherein the agent is selected from the group consisting of antibodies that bind survivin, survivin binding partners, and nucleic acids that hybridize to the nucleic acid encoding survivin.
18. The kit of claim 17 , wherein the agent is tagged with a label.
19. The kit of claim 17 , wherein the label is a radioactive label, a fluorescent label, an enzyme, or a chemiluminescent tag.
20. The kit of claim 16 , wherein the agent is packaged in an aqueous medium or in lyophilized form.
21. The kit of claim 16 , further comprising a component for analyzing the presence of survivin.
22. The kit of claim 16 , wherein the cancer is bladder or prostate cancer.
23. A method of determining the grade of a cancer in a patient comprising quantitating the amount of survivin in a sample of urine supernatant from a patient and comparing the amount of survivin in the sample with the amount of survivin in control samples to determine the grade of the cancer in the patient.
24. A method of determining the stage of a cancer in a patient comprising quantitating the amount of survivin in a sample of wine supernatant from a patient and comparing the amount of survivin in the sample with the amount of survivin in control samples to determine the stage of the cancer in the patient.
25. A method of monitoring cancer in a patient comprising quantitating the amount of survivin in a sample of urine supernatant from a patient and comparing the amount of survivin in the sample with the amount of survivin in control samples to determine the grade of the cancer in the patient, thereby monitoring cancer in a patient.
26. The method of claim 1 , wherein the cancer is any cancer that expresses survivin.
27. The method of claim 1 , wherein the cancer is new onset cancer or recurrent cancer.
28. The method of claim 23 , wherein the amount of survivin is quantitated by detecting survivin RNA.
29. The method of claim 28 , wherein the survivin RNA is detected by nucleic acid hybridization.
30. The method of claim 29 , wherein the nucleic acid hybridization is RT-PCR or Northern blot analysis.
31. The method of claim 24 , wherein the amount of survivin is quantitated by detecting survivin RNA.
32. The method of claim 31 , wherein the survivin RNA is detected by nucleic acid hybridization.
33. The method of claim 32 , wherein the nucleic acid hybridization is RT-PCR or Northern blot analysis.
34. The method of claim 25 , wherein the amount of survivin is quantitated by detecting survivin RNA.
35. The method of claim 34 , wherein the survivin RNA is detected by nucleic acid hybridization.
36. The method of claim 35 , wherein the nucleic acid hybridization is RT-PCR or Northern blot analysis.
37. The method of claim 1 , wherein the presence or absence of is detected by detecting the presence or absence of survivin RNA.
38. The kit of claim 16 , wherein the presence of survivin is detected by detecting survivin RNA.