IP Library Granted Patent US 7,022,472
Granted Patent B2
US 7,022,472 · App. 09/426,548 · Granted Apr 4, 2006

Mutations in human MLH1 and human MSH2 genes useful in diagnosing colorectal cancer

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Quick Facts
Patent No.
US 7,022,472
App. No.
09/426,548
Granted
Apr 4, 2006
Kind
B2
Abstract

Variant human MLH1 and MSH2 genes are provided. Methods of using these variant genes to diagnose hereditary non-polyposis colorectal cancer (HNPCC) and/or determine a patient's susceptibility to developing HNPCC are also provided. Methods and compositions for identifying new variant MLH1 of MSH2 genes are also provided. In addition, experimental models for hereditary non-polyposis colorectal cancer comprising these variant genes are provided.

Claims (19)

1. A method of diagnosing hereditary non-polyposis colorectal cancer in a patient comprising:

(a) obtaining a DNA or RNA sample from a patient; and

(b) screening the DNA or RNA sample with an oligonucleotide probe to detect a hMLH1 mutant 1, a hMSH2 mutant 1, a hMSH2 mutant 2, or a hMSH2 mutant 3, wherein binding of the oligonucleotide probe to the DNA or RNA sample is indicative of the presence of the hMLH1 mutant 1, the hMSH2 mutant 1, the hMSH2 mutant 2, or the hMSH2 mutant 3 and hereditary non-polyposis colorectal cancer.

2. The method of claim 1 wherein the oligonucleotide probe detects a hMLH1 mutatn 1.

3. The method of claim 1 wherein the oligonucleotide probe detects a hMSH2 mutant 1.

4. The method of claim 1 wherein the oligonucleotide probe detets a hMSH2 mutant 2.

5. The method of claim 1 wherein the oligonucleotdie probe detects a hMSH2 mutant 3.

6. A method for predicting susceptibility of a patient to developing hereditary non-polyposis colorectal cancer comprising:

(a) obtaining a DNA or RNA sample from a patient; and

(b) screening the DNA or RNA sample with an oligonucleotide probe to detect a hMLH1 mutant 1, a hMSH2 mutant 1, a hMSH2 mutant 2, or a hMSH2 mutant 3, wherein binding of the oligonucleotide probe to the DNA or RNA sample is indicative of the presence of the hMLH1 mutant 1, the hMSH2 mutant 1, the hMSH2 mutant 2, or the hMSH2 mutant 3 and hereditary non-polyposis colorectal cancer.

7. The method of claim 6 wherein the oligonucleotide probe detects a hMLH1 mutant 1.

8. The method of claim 6 wherein the oligonucleotide probe detects a hMSH2 mutant 1.

9. The method of claim 6 wherein the oligonucleotide probe dtectes a hMSH2 mutant 2.

10. The method of claim 6 wherein the oligonucleotide probe detects a hMSH2 mutant 3.

11. An oligonucleotide probe fully complimentary to a sequence comprising a hMLH1 mutant 1, hMSH2 mutant 1, a hMSH2, or hMSH2 mutant 3 in the DNA or RNA sample.

12. The oligonucleotide probe of claim 11 wherein the oligonucleotide probe is fully complementary to a sequence comprising a hMLH1 mutant 1.

13. The Oligonucleotide probe of claim 11 wherein the oligonucleotide probe is fully complementary to a sequence comprising a hMSH2 mutant 1.

14. The oligoncleotide probe of claim 11 wherein the oligonucleotide probe is fully complementary to a sequence comprising a hMSH2 mutant 2.

15. The oligonuleotide probe of claim 11 wherein the oligonucleotide probe is fully complementary to a sequence comprising a hMSH2 mutant 3.

Assignments (2)
CHANGE OF NAME Recorded Nov 28, 2000
From: DIADEXUS, LLC
To: DIADEXUS, INC.
Reel/Frame 011139/0592 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2000
From: ROBBINS, DAVID; LIN-GOERKE, JUILI LILLIAN; LING, JESSICA C.
To: DIADEXUS, LLC
Reel/Frame 010566/0127 →