IP Library Granted Patent US 9,029,340
Granted Patent B2
US 9,029,340 · App. 13/811,442 · Granted May 12, 2015

Radiation sensitization agents for prostate cancer

Inventors: Shawn Edward Lupold (Ellicott City, MD); Theodore L. DeWeese (Baltimore, MD); Xiaohua Ni (Baltimore, MD); Yonggang Zhang (Nottingham, MD)
Assignee: The Johns Hopkins University
A61K48/005
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Quick Facts
Patent No.
US 9,029,340
App. No.
13/811,442
Granted
May 12, 2015
Kind
B2
Abstract

Compositions and methods are provided for sensitizing neoplastic cells to radiotherapy. The invention provides aptamer-inhibitory nucleic acid chimeras that selectively inliibit the expression of radiosensitizing genes in neoplastic cells expressing a cell surface molecule that binds the aptamer.

Claims (18)

1. A method of inducing cell death or terminal differentiation in a neoplastic cell, the method comprising:

a) contacting the neoplastic cell with an effective amount of an aptamer-inhibitory nucleic acid chimera, wherein the aptamer-inhibitory nucleic acid chimera comprises a 2′fluoro-modified pyrimidine RNA aptamer-shRNA chimera, wherein the aptamer-shRNA chimera specifically binds prostate-specific membrane antigen (PSMA), and wherein the shRNA decreases the expression of DNA-activated protein kinase (DNAPK); and

b) exposing the neoplastic cell to ionizing radiation, thereby inducing cell death or terminal differentiation in the neoplastic cell.

2. A method of reducing the growth, proliferation or survival of a neoplastic cell, the method comprising:

a) contacting the neoplastic cell with an effective amount of an aptamer-inhibitory nucleic acid chimera, wherein the aptamer-inhibitory nucleic acid chimera comprises a 2′fluoro-modified pyrimidine RNA aptamer-shRNA chimera, wherein the aptamer-shRNA chimera specifically binds prostate-specific membrane antigen (PSMA), and wherein the shRNA decreases the expression of DNA-activated protein kinase (DNAPK); and

b) exposing the neoplastic cell to ionizing radiation, thereby reducing growth, proliferation or survival of the neoplastic cell.

3. A method of treating neoplasia in a subject comprising:

a) administering an aptamer-inhibitory nucleic acid chimera to the subject, wherein the aptamer-inhibitory nucleic acid chimera comprises a 2′fluoro-modified pyrimidine RNA aptamer-shRNA chimera, wherein the aptamer-shRNA chimera specifically binds prostate-specific membrane antigen (PSMA), and wherein the shRNA decreases the expression of DNA-activated protein kinase (DNAPK); and

b) exposing the neoplasia to ionizing radiation, thereby treating neoplasia in the subject.

4. A method of treating prostate cancer in a subject in need thereof comprising:

a) administering an aptamer-shRNA chimera to the subject, wherein the aptamer-shRNA chimera comprises a 2′fluoro-modified pyrimidine RNA aptamer-shRNA chimera, wherein the aptamer-shRNA chimera specifically binds prostate-specific membrane antigen (PSMA), and wherein the shRNA decreases the expression of DNA-activated protein kinase (DNAPK); and

b) exposing the subject to ionizing radiation, thereby treating prostate cancer in the subject.

5. The method of claim 4 , wherein the aptamer-shRNA chimera comprises an A10-3 aptamer, wherein the A10-3 aptamer comprises SEQ ID NO: 11 or SEQ ID NO: 63.

6. The method of claim 4 , wherein the aptamer-shRNA chimera comprises A10-3 aptamer-DNAPK shRNA, wherein said A10-3 aptamer-DNAPK shRNA comprises SEQ ID NO: 44.

7. The method of claim 4 , wherein the DNAPK shRNA comprises SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 64, or SEQ ID NO: 65.

8. The method of claim 1 , wherein the aptamer-shRNA chimera comprises an A10-3 aptamer, wherein the A10-3 aptamer comprises SEQ ID NO: 11 or SEQ ID NO: 63.

9. The method of claim 1 , wherein the shRNA comprises SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 64, or SEQ ID NO: 65.

10. The method of claim 1 , wherein the aptamer-shRNA chimera comprises A10-3 aptamer-DNAPK shRNA, wherein said A10-3 aptamer-DNAPK shRNA comprises SEQ ID NO: 44.

Continuity (2)
Provisional Application 61366734 · Jul 22, 2010
Related Publication 20130123566A1 · May 16, 2013