IP Library Granted Patent US 8,658,362
Granted Patent B2
US 8,658,362 · App. 13/406,615 · Granted Feb 25, 2014

Methods for diagnosing colon cancer using MicroRNAs

Inventors: Carlo M. Croce (Columbus, OH); George A. Calin (Pearland, TX); Stefano Volinia (Ferrara, IT)
Assignee: The Ohio State University
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Quick Facts
Patent No.
US 8,658,362
App. No.
13/406,615
Granted
Feb 25, 2014
Kind
B2
Abstract

The present invention provides novel methods and compositions for the diagnosis and treatment of solid cancers. The invention also provides methods of identifying inhibitors of tumorigenesis.

Claims (34)

1. A method of diagnosing whether a subject has, or is at risk for developing, colon cancer, comprising:

extracting a test sample from a subject having, or suspected of having, colon cancer, wherein the sample is extracted from colon tissue;

measuring, by hybridization assay, the level of at least one miR gene product of miR-24-1 in the test sample;

comparing the level of at least one miR-24-1 gene product in the test sample to a control level of at least one corresponding miR gene product;

correlating an increase in the test sample level of miR-24-1 gene product compared to the level of miR-24-1 gene product in the control sample with a subject having, or being at risk for developing, colon cancer; and

diagnosing the subject as having, or being at risk for developing, colon cancer, if the level of the at least one miR gene product in the test sample from the subject is greater than the control level of the corresponding miR gene product;

wherein an increase in the level of miR-24-1 gene product in the test sample, relative to the control level of the at least one corresponding miR gene product, is indicative of the subject having, or being at risk for developing, colon cancer.

2. A method of claim 1 , which further comprises:

comparing the level of at least one additional miR gene product in the test sample from the subject to a control level of the miR gene product, wherein the at least one additional miR gene product is selected from the group consisting of: miR-21; miR-17-5p; miR-191; miR-29b-2; miR-223; miR-128b; miR-199a-1; miR-24-2; miR-146; miR-155; miR-181b-1; miR-20a; miR-107; miR-32; miR-92-2; miR-214; miR-30c; miR-25; miR-221; and miR-106a.

3. A method of claim 1 , which further comprises:

comparing the level of at least one additional miR gene product in the test sample from the subject to a control level of the miR gene product, wherein the at least one additional miR gene product is selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

4. A method of claim 1 , which further comprises:

comparing the level of at least two additional miR gene products in the test sample from the subject to a control level of the corresponding miR gene products, wherein the at least two additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

5. A method of claim 1 , which further comprises:

comparing the level of at least three additional miR gene products in the test sample from the subject to a control level of the corresponding miR gene products, wherein the at least three additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

6. A method of claim 1 , which further comprises:

comparing the level of at least four additional miR gene products in the test sample from the subject to a control level of the corresponding miR gene products, wherein the at least four additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

7. A method of claim 1 , which further comprises:

comparing the level of at least five additional miR gene products in the test sample from the subject to a control level of the corresponding miR gene products, wherein the at least five additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

8. A method of diagnosing whether a subject has, or is at risk for developing, colon cancer, comprising:

obtaining a test sample from a subject having, or suspected of having, colon cancer, wherein the test sample comprises colon tissue;

reverse transcribing at least one miR gene product of miR-24-1 from the test sample to provide at least one corresponding miR gene product target oligonucleotides;

hybridizing target oligodeoxynucleotides to a microarray comprising miRNA-specific probe oligonucleotides that include at least one corresponding to miR-24-1 miRNA-specific probe oligonucleotides to provide a hybridization profile for the test sample;

comparing the signal of the at least one miR gene product of miR-24-1 in the test sample hybridization profile to the signal of a corresponding miR-24-1 miRNA in a control hybridization profile;

correlating an increase in the signal of the at least miR-24-1 in the test sample hybridization profile compared to the signal of the corresponding miR-24-1 in the control hybridization profile with a subject having, or being at risk for developing, colon cancer; and

diagnosing the subject as having, or being at risk for developing, colon cancer, if the level of miR gene product of miR-24-1 in the test sample hybridization profile is greater than the level of miR gene product of miR-24-1 in the control hybridization profile;

wherein an increase in the level of miR-24-1 gene product in the test sample, relative to the control level of miR-24-1 gene product, is indicative of the subject having, or being at risk for developing, colon cancer.

9. A method of claim 8 , which further comprises: comparing a hybridization profile of at least one additional miR gene product in the test sample from the subject to a control hybridization profile of the miR gene product, wherein the at least one additional miR gene product is selected from the group consisting of: miR-21; miR-17-5p; miR-191; miR-29b-2; miR-223; miR-128b; miR-199a-1; miR-24-2; miR-146; miR-155; miR-181b-1; miR-20a; miR-107; miR-32; miR-92-2; miR-214; miR-30c; miR-25; miR-221; and miR-106a.

10. A method of claim 8 , which further comprises: comparing a hybridization profile of at least one additional miR gene product in the test sample from the subject to a control hybridization profile of the corresponding miR gene product, wherein the at least one additional miR gene product is selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

11. A method of claim 8 , which further comprises: comparing a hybridization profile of at least two additional miR gene products in the test sample from the subject to a control hybridization profile of the corresponding miR gene products, wherein the at least two additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

12. A method of claim 8 , which further comprises: comparing a hybridization profile of at least three additional miR gene products in the test sample from the subject to a control hybridization profile of the corresponding miR gene products, wherein the at least three additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

13. A method of claim 8 , which further comprises: comparing a hybridization profile of at least four additional miR gene products in the test sample from the subject to a control hybridization profile of the corresponding miR gene products, wherein the at least four additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

14. A method of claim 8 , which further comprises: comparing a hybridization profile of at least five additional miR gene products in the test sample from the subject to a control hybridization profile of the corresponding miR gene products, wherein the at least five additional miR gene products are selected from the group consisting of: miR-29b-2; miR-20a; miR-10a; miR-32; miR-203; miR-106a; miR-17-5p; miR-30c; miR-223; miR-126; miR-128b; miR-21; miR-24-2; miR-99b prec; miR-155; miR-213; miR-150; miR-107; miR-191; miR-221; and miR-9-3.

15. A method of claim 1 , further comprising communicating a result of the diagnosing to at least one person.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 24, 2015
From: OHIO STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036687/0033 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2012
From: CROCE, CARLO M.; CALIN, GEORGE A.; VOLINIA, STEFANO
To: THE OHIO STATE UNIVERSITY
Reel/Frame 027819/0315 →
Continuity (3)
Division 12160061
Provisional Application 60756585 · Jan 5, 2006
Related Publication 20120214694A1 · Aug 23, 2012