IP Library Granted Patent US 8,603,758
Granted Patent B2
US 8,603,758 · App. 13/532,364 · Granted Dec 10, 2013

Prostate carcinogenesis predictor

Inventors: Mildred Acevedo-Duncan (Plant City, FL); Hla Y. Win (Tampa, FL); Raoul Salup (Tampa, FL)
Assignees: University of South Florida; The United States of America as represented by the Department of Veterans Affairs
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,603,758
App. No.
13/532,364
Granted
Dec 10, 2013
Kind
B2
Abstract

A method of detecting prostate tumorigenesis in a subject, the method including the steps of (a) obtaining a sample from the prostate of the human subject, (b) detecting quantitatively or semi-quantitatively in the sample a level of expression for PKC-ι and (c) comparing the expression level in (b) to a level of expression in a normal control, wherein overexpression of PKC-ι, with respect to the control, indicates the presence of prostate cancer in the subject. The present invention is based upon the discovery that PKC-ι levels are elevated during prostate tumorigenesis. Furthermore, the proliferation rate of the tumor correlates with the level of PKC-ι. The invention also provides methods of treating prostate cancer by administering to the subject a compound that inhibits the expression of PKC-ι. The compound can be a small interfering RNA (siRNA) molecule.

Claims (24)

1. A method of diagnosing prostate cancer in a subject comprising:

(a) obtaining a tissue sample from the prostate of a human subject;

(b) determining in the sample a level of expression for PKC-ι, wherein said determining step comprises:

contacting the sample with an antibody that recognizes PKC-ι protein in an immunoassay selected from western blot assay, enzyme-linked immunosorbent assay (ELISA), and immunohistochemical assay, and

detecting the complex between the antibody and the PKC-ι protein;

(c) comparing the expression level determined in (b) to a control, wherein the control is a level of expression of PKC-ι in a benign human prostate tissue; and

(d) informing the human subject as having prostate cancer if the PKC-ι expression level determined in (b) is higher than the control or informing the human subject as not having prostate cancer if the PKC-ι expression level determined in (b) is lower than the control.

2. The method according to claim 1 wherein the determining determines the quantitative level of expression of PKC-ι in a prostate sample tissue.

3. The method according to claim 1 wherein said antibody is a monoclonal antibody.

4. The method according to claim 1 wherein said antibody is a polyclonal antibody.

5. The method according to claim 1 wherein said protein is contacted with said antibody in an enzyme-linked immunosorbent assay (ELISA).

6. The method according to claim 1 wherein said immunoassay is a western blot assay.

7. A method of providing treatment of prostate cancer to a human subject, comprising:

(a) obtaining a tissue sample from the prostate of a human subject;

(b) determining in the sample a level of expression for PKC-ι,wherein said determining: step comprises:

contacting the sample with an antibody which recognizes PKC-ι protein; and

detecting the complex between the antibody and the PKC-ι protein;

(c) comparing the expression level determined in (b) to a control, wherein the control is a level of expression of PKC-ι in a benign human prostate tissue; and

(d) providing treatment of prostate cancer to the human subject if the PKC-ι expression level determined in (b) is higher than the control.

8. The method according to claim 7 wherein said antibody is a monoclonal antibody.

9. The method according to claim 7 wherein said antibody is a polyclonal antibody.

10. The method according to claim 7 wherein said protein is contacted with said antibody in an immunoassay selected from the group consisting of radioimmunoassay, western blot assay, immunofluorescent assay, enzyme immunoassay, enzyme-linked immunosorbent assay (ELISA), immunoprecipitation, chemiluminescent assay, immunohistochemical assay, dot blot assay and slot blot assay.

11. The method according to claim 10 wherein said immunoassay is a western blot assay.

12. The method according to claim 10 wherein said immunoassay is an enzyme-linked immunosorbent assay (ELISA).

Continuity (3)
Division 12253663 · Oct 17, 2008
Provisional Application 60980611 · Oct 17, 2007
Related Publication 20120294932A1 · Nov 22, 2012