Therapies for cancer using RLIP76
The present invention is a composition identified as a region of ralA binding protein 1, wherein the region neighbors a membrane-associated portion of the ralA binding protein 1, reduces transport activity and membrane association of the ralA binding protein 1 and kills cells undergoing uncontrolled cell growth in a subject that has cells undergoing uncontrolled cell growth. The region is used to generate medicines that kill malignant cells and tumorigenic cells. Medicines may be in the form of antibodies, si-RNA and small molecules that recognize the region.
1. A method of inhibiting growth of a malignant cell expressing RLIP76 comprising contacting the cell expressing RLIP76 with a composition that inhibits expression of RLIP76, wherein the composition comprises a proteoliposome, and wherein the composition comprises an anti-sense nucleic acid or double stranded siRNA molecule that targets nucleotides encoding a region of RLIP76 selected from the group consisting of SEQ ID NO:3, and SEQ ID NO:4.
2. The method of claim 1 , wherein the anti-sense nucleic acid is in a composition comprising a pharmaceutically acceptable carrier.
3. The method of claim 1 , wherein the composition comprises a liposome anti-sense nucleic acid that has the nucleic acid sequence of SEQ ID NO:5.
4. The method of claim 1 , wherein the malignant cell is a melanoma cell, a small cell lung cancer cell, a non-small cell lung cancer cell, an ovarian cancer cell, a prostate cancer cell or an adenocarcinoma cell.
5. The method of claim 1 , wherein the malignant cell is a melanoma cell.
6. The method of claim 1 , wherein the cell is in a subject.
7. The method of claim 1 , wherein the cell is in a human subject.
8. A method of inhibiting growth of a malignant cell expressing RLIP76 in a subject comprising: administering to the subject a pharmaceutically acceptable composition comprising an effective amount of an anti-sense nucleic acid that is effective to inhibit expression of RLIP76 in the malignant cell, wherein the pharmaceutically acceptable composition comprises a liposome, and wherein the anti-sense nucleic acid targets nucleotides encoding a region of RLIP76 selected from the group consisting of SEQ ID NO:4, and SEQ ID NO:3.
9. The method of claim 8 , wherein the anti-sense nucleic acid is complementary to an mRNA that encodes SEQ ID NO:22.
10. The method of claim 8 , wherein the malignant cell is a melanoma cell, a small cell lung cancer cell, a non-small cell lung cancer cell, an ovarian cancer cell, a prostate cancer cell or an adenocarcinoma cell.
11. The method of claim 8 , wherein the malignant cell is a melanoma cell.