IP Library Granted Patent US 8,741,573
Granted Patent B2
US 8,741,573 · App. 12/377,073 · Granted Jun 3, 2014

Consensus coding sequences of human breast and colorectal cancers

Inventors: Tobias Sjoblom (Baltimore, MD); Sian Jones (Baltimore, MD); D. Williams Parsons (Baltimore, MD); Laura D. Wood (Baltimore, MD); Jimmy Lin (Baltimore, MD); Thomas Barber (Baltimore, MD); Diana Mandelker (Baltimore, MD); Bert Vogelstein (Baltimore, MD); Kenneth W. Kinzler (Baltimore, MD); Victor E. Velculesu (Baltimore, MD)
Assignee: The Johns Hopkins University
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 8,741,573
App. No.
12/377,073
Granted
Jun 3, 2014
Kind
B2
Abstract

Analysis of 13,023 genes in 11 breast and 11 colorectal cancers revealed that individual tumors accumulate an average of ˜90 mutant genes but that only a subset of these contribute to the neoplastic process. Using stringent criteria to delineate this subset, we identified 189 genes (average of 11 per tumor) that were mutated at significant frequency. The vast majority of these genes were not known to be genetically altered in tumors and are predicted to affect a wide range of cellular functions, including transcription, adhesion, and invasion. These data define the genetic landscape of two human cancer types, provide new targets for diagnostic and therapeutic intervention and monitoring.

Claims (28)

1. A method of testing a human sample, comprising the steps of:

assaying a test colorectal sample or a suspected colorectal cancer metastasis relative to a normal sample of the human and determining a somatic K117mutation in KRAS gene or its encoded cDNA or protein.

2. The method of claim wherein the normal sample is a colorectal tissue sample.

3. The method of claim 1 wherein the mutation is assayed and determined in the gene.

4. The method of claim 1 wherein the mutation is assayed and determined in the cDNA.

5. The method of claim 1 wherein the mutation is assayed and determined in the protein.

6. The method of claim 1 wherein the step of testing comprises sequencing all or part of the gene.

7. The method of claim 1 wherein the step of testing employs a mutation specific probe.

8. The method of claim 1 wherein the step of testing employs a mutation specific primer.

9. The method of claim 1 wherein the step of testing employs a mutation specific antibody.

10. The method of claim 1 wherein the step of testing employs an amplification reaction.

11. The method of claim 1 wherein the step of testing employs an antibody-antigen reaction.

12. The method of claim 1 wherein the step of testing employs a hybridization reaction.

13. The method of claim 1 wherein the step of testing employs a primer extension reaction.

14. A method of characterizing a colorectal cancer in a human, comprising the steps of:

assaying and determining in a test colorectal cancer sample or a suspected colorectal cancer metastasis relative to a normal sample of the human, a somatic K117 mutation in KRAS gene or its encoded cDNA or protein.

15. The method of claim 14 wherein the normal sample is a colorectal tissue sample.

16. The method of claim 14 wherein the mutation is assayed and determined in the gene.

17. The method of claim 14 wherein the mutation is assayed and determined in the cDNA.

18. The method of claim 14 wherein the mutation is assayed and determined in the protein.

19. The method of claim 14 wherein the step of testing comprises sequencing all or part of the gene.

20. The method of claim 14 wherein the step of testing employs a mutation specific probe.

21. The method of claim 14 wherein the step of testing employs a mutation specific primer.

22. The method of claim 14 wherein the step of testing employs a mutation specify antibody.

23. The method of claim 14 wherein the step of testing employs an amplification reaction.

24. The method of claim 14 wherein the step of testing employs an antibody-antigen reaction.

25. The method of claim 14 wherein the step of testing employs a hybridization reaction.

26. The method of claim 14 wherein the step of testing employs a primer extension reaction.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 28, 2017
From: JOHNS HOPKINS UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044968/0842 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR: TOBIAS SJOBLON PREVIOUSLY RECORDED ON REEL 024916 FRAME 0965. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNOR: TOBIAS SJOBLOM. Recorded Oct 12, 2010
From: SJOBLOM, TOBIAS; PARSONS, D. WILLIAMS; JONES, SIAN; WOOD, LAURA D.; LIN, JIMMY; MANDELKER, DIANA; VOGELSTEIN, BERT; KINZLER, KENNETH W.; VELCULESU, VICTOR E.; BARBER, THOMAS
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 025122/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2010
From: SJOBLON, TOBIAS; PARSONS, D. WILLIAMS; JONES, SIAN; WOOD, LAURA D.; LIN, JIMMY; MANDELKER, DIANA; VOGELSTEIN, BERT; KINZLER, KENNETH W.; VELCULESU, VICTOR E.; BARBER, THOMAS
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 024916/0965 →
Continuity (3)
Provisional Application 60836944 · Aug 11, 2006
Provisional Application 60842363 · Sep 6, 2006
Related Publication 20100316995A1 · Dec 16, 2010