IP Library Granted Patent US 8,551,720
Granted Patent B2
US 8,551,720 · App. 12/739,371 · Granted Oct 8, 2013

Methods for diagnosing bowel disease

Inventor: Deliang Cao (Chatham, IL)
Assignee: The Board of Trustees of Southern Illinois University
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Quick Facts
Patent No.
US 8,551,720
App. No.
12/739,371
Granted
Oct 8, 2013
Kind
B2
Abstract

Provided herein are methods and materials for diagnosing a bowel disease in a subject by detecting the presence or absence of a bowel disease marker. A bowel disease marker has been identified as AKR1B10 and may be useful in identifying subjects at risk for bowel disease, predicting bowel disease progression, and assessing a subject's response to therapy.

Claims (26)

1. A method for detecting, and/or monitoring, a non-cancerous colorectal disease in a subject, comprising:

(a) providing a sample from a subject;

(b) measuring an amount of a BD-marker protein in the subject sample using an immunoassay;

(c) measuring an amount of BD-marker protein in a control sample using the immunoassay;

(d) comparing the amount from (b) to the amount from (c) to detect a difference between the amount of the BD-marker protein in the control sample and the amount of the BD-marker protein in the subject sample; and

(e) diagnosing the subject as having a non-cancerous colorectal disease when the difference detected in step (d) shows a loss of the BD-marker protein or a reduction in the amount of the BD-marker protein in the subject sample relative to the amount of the BD-marker protein in the control sample, wherein the BD-marker protein is AKR1B10, and further wherein the non-cancerous colorectal disease is selected from the group consisting of non-cancerous rectal disease, non-cancerous chronic colorectal disease, non-cancerous chronic inflammatory bowel disease, adenoma, inflammatory bowel disease, ulcerative colitis, and Crohn's disease.

2. The method of claim 1 , wherein the control sample is from a subject that does not have a colorectal disease.

3. The method of claim 1 , wherein the control sample is taken from the subject being monitored.

4. The method of claim 3 , wherein the control sample is taken before the subject sample is taken.

5. The method of claim 1 , wherein the sample comprises protein.

6. The method of claim 1 , wherein the amount of AKR1B10 in the subject sample is lower than the amount of AKR1B10 in the control sample.

7. The method of claim 6 , wherein the amount of AKR1B10 in the subject sample is between 1 and 40-fold lower than the amount of AKR1B10 in the control sample.

8. The method of claim 1 , wherein the sample comprises a stool sample.

9. The method of claim 8 , wherein the amount of AKR1B10 marker protein is determined by the immunoassay in which the sample is contacted by an antibody which specifically binds to AKR1B10.

10. The method of claim 9 , wherein the immunoassay is an ELISA.

11. The method of claim 1 , wherein the sample from the subject comprises a tissue sample.

12. The method of claim 11 , wherein the amount of AKR1B10 marker protein is determined by an assay selected from the group consisting of: Western blot and immunohistochemistry.

13. A method for detecting or monitoring a non-cancerous colorectal disease in a subject, comprising:

(a) providing a sample from a subject;

(b) measuring an amount of AKR1B10 marker protein in the subject sample; and

(c) diagnosing the subject as having the non-cancerous colorectal disease when the amount of AKR1B10 marker protein is not detectable in the subject sample, wherein the non-cancerous colorectal disease is at least one of rectal disease, chronic colorectal disease, chronic inflammatory bowel disease, adenoma, inflammatory bowel disease, ulcerative colitis, and Crohn's disease.

14. The method of claim 13 , wherein the sample from the subject comprises a stool sample.

15. The method of claim 14 , wherein the amount of AKR1B10 marker protein is determined by the immunoassay in which the sample is contacted by an antibody which specifically binds to AKR1B10.

16. The method of claim 15 , wherein the immunoassay is an ELISA.

17. The method of claim 13 , wherein the sample from the subject comprises a tissue sample.

18. The method of claim 17 , wherein the amount of AKR1B10 marker protein is determined by an assay selected from the group consisting of: Western blot and immunohistochemistry.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 14, 2013
From: SOUTHERN ILLINOIS UNIVERSITY SCH OF MED
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031637/0505 →
CONFIRMATORY LICENSE Recorded May 21, 2010
From: SOUTHERN ILLINOIS UNIVERSITY SCH OF MED
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024423/0922 →
Continuity (2)
Provisional Application 61000440 · Oct 25, 2007
Related Publication 20100256009A1 · Oct 7, 2010