IP Library Granted Patent US 8,283,459
Granted Patent B2
US 8,283,459 · App. 11/974,481 · Granted Oct 9, 2012

Kinase suppressor of Ras inactivation for therapy of Ras mediated tumorigenesis

Assignee: Memorial Sloan-Kettering Cancer Center
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Quick Facts
Patent No.
US 8,283,459
App. No.
11/974,481
Granted
Oct 9, 2012
Kind
B2
Abstract

The present invention relates to methods and compositions for the specific inhibition of kinase suppressor of Ras (KSR). In particular, the invention provides genetic approaches and nucleic acids for the specific inhibition of KSR, particularly of KSR expression. The invention relates to antisense oligonucleotides and the expression of nucleic acid which is substantially complementary to KSR RNA. Oligonucleotide and nucleic acid compositions are provided. The invention provides methods to inhibit KSR, including inhibition of KSR expression. Methods for blocking gf Ras mediated tumorigenesis, metastasis, and for cancer therapy are provided. Methods for conferring radiosensitivity to cells are also provided.

Claims (11)

1. A pharmaceutical composition comprising a therapeutically effective amount of an antisense oligonucleotide comprising a sequence that is about 90% to 100% complementary to nucleotide SEQ ID NO:5 and a pharmaceutically acceptable carrier or diluent, wherein said oligonucleotide is from 8 to about 50 nucleotides in length.

2. The pharmaceutical composition of claim 1 , wherein the oligonucleotide is labeled with a detectable label.

3. The pharmaceutical composition of claim 2 , wherein the label is selected from enzymes, ligands, chemicals which fluoresce and radioactive elements.

4. The pharmaceutical composition of claim 1 , wherein said oligonucleotide comprises at least one phosphorothioate linkage.

5. The pharmaceutical composition of claim 1 comprising a recombinant DNA molecule comprising the oligonucleotide.

6. The pharmaceutical composition of claim 5 , wherein the oligonucleotide is operatively linked to a transcription control sequence.

7. The pharmaceutical composition of claim 1 , wherein said oligonucleotide is from 10 to 30 nucleotides in length.

8. The pharmaceutical composition of claim 1 , wherein said oligonucleotide is from 15 to 25 nucleotides in length.

9. The pharmaceutical composition of claim 1 , wherein the sequence that is about 95% to 100% complementary to nucleotide SEQ ID NO:5.

10. A cell line transfected with a recombinant DNA molecule comprising an antisense oligonucleotide comprising a sequence that is about 90% to 100% complementary to nucleotide SEQ ID NO:5, wherein said oligonucleotide is from 8 to about 50 nucleotides in length, wherein the oligonucleotide is operatively linked to a transcription control sequence.

11. An expression vector expressing an antisense oligonucleotide comprising a sequence that is about 90% to 100% complementary to nucleotide SEQ ID NO:5, wherein said oligonucleotide is from 8 to about 50 nucleotides in length.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 30, 2015
From: SLOAN-KETTERING INST CAN RESEARCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035336/0812 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2007
From: KOLESNCIK, RICHARD N.; XING, HONGMEI R.
To: MEMORIAL SLOAN-KETTERING CANCER CENTER
Reel/Frame 020014/0642 →
Continuity (4)
Continuation In Part PCTUS0316961 · May 29, 2003
Provisional Application 60384228 · May 30, 2002
Provisional Application 60460023 · Apr 3, 2003
Related Publication 20090143320A1 · Jun 4, 2009