Radiation sensitization agents for prostate cancer
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.
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.