IP Library Granted Patent US 8,852,870
Granted Patent B2
US 8,852,870 · App. 12/999,389 · Granted Oct 7, 2014

Systems and methods for diagnosis and prognosis of cancer

Inventors: Vaclav Vetvicka (Louisville, KY); Martin Fusek (Tursko, CZ); Jarmila Zidkova (Prague, CZ)
Assignee: University of Louisville Research Foundation, Inc.
G01N33/574G01N33/564G01N2333/96416
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 8,852,870
App. No.
12/999,389
Granted
Oct 7, 2014
Kind
B2
Abstract

Methods for diagnosing a cancer in a subject are provided that include determining an amount of autoantibodies immunoreactive to procathepsin D (pCD) in a sample obtained from the subject. Further provided are systems for diagnosing a cancer in a subject that include an autoantibody immunoreactive pCD antigen and a means for detecting binding of an autoantibody to the antigen.

Claims (13)

1. A method for determining an amount of autoantibodies immunoreactive to an antigen present in a biological sample of a subject, comprising:

providing a biological sample from the subject;

contacting an antigen with the biological sample, wherein the antigen consists of a peptide of SEQ ID NO:2, or consists of a plurality of peptides of SEQ ID NO: 2;

detecting the autoantibodies in the sample immunoreactive to the antigen; and

determining an amount in the sample of autoantibodies immunoreactive to procathepsin D (pCD) based on the autoantibodies detected.

2. The method of claim 1 , wherein the biological sample comprises blood, plasma, serum, urine, cerebrospinal fluid, saliva, or breast milk.

3. The method of claim 1 , wherein the antigen consists of a plurality of peptides of SEQ ID NO: 2.

4. The method of claim 1 , further comprising determining the subject may have cancer by comparing the amount of the autoantibodies in the sample, if present, to a control level of the autoantibodies, wherein the subject is determined to have the cancer if there is a measurable difference in the amount of the autoantibodies in the sample as compared to the control level.

5. The method of claim 4 , wherein the cancer is selected from the group consisting of breast cancer, lung cancer, ovarian cancer, colon cancer, rectal cancer, and cervical cancer.

6. The method of claim 5 , wherein the cancer is breast cancer.

7. The method of claim 4 , further comprising selecting a treatment or modifying a treatment for the cancer based on the determined amount of the autoantibodies.

8. The method of claim 4 , further comprising characterizing a cancer based on the determined amount of autoantibodies.

9. The method of claim 8 , wherein characterizing the cancer comprises determining a stage of the cancer.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 24, 2011
From: UNIVERSITY OF LOUISVILLE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025841/0359 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2010
From: VETVICKA, VACLAV
To: UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.
Reel/Frame 025510/0025 →
Continuity (2)
Provisional Application 61061834 · Jun 16, 2008
Related Publication 20110081669A1 · Apr 7, 2011