Claims
- 1. A method for measuring the expression level of serine palmitoyltransferase by mammalian cells comprising:
(a) contacting a serine palmitoyltransferase specific compound with a mammalian cell to form a plurality of compound-serine palmitoyltransferase complexes; and, (b) measuring the level of serine palmitoyltransferase expressed by the cell by detecting the presence of the complexes.
- 2. A method for measuring the expression of serine palmitoyltransferase by mammalian cells comprising:
(a) contacting a serine palmitoyltransferase specific compound with a first mammalian cell which basally expresses serine palmitoyltransferase to form a first plurality of compound-serine palmitoyltransferase complexes; (b) contacting a serine palmitoyltransferase specific compound with a second mammalian cell which hyperproliferatively expresses serine palmitoyltransferase to form a second plurality of compound-serine palmitoyltransferase complexes; (c) determining the levels of serine palmitoyltransferase expressed by the first and second cells by detecting the presence of the first and second plurality of complexes; and (d) measuring the difference in the levels of serine palmitoyltransferase expressed by the first and second cells.
- 3. A method for in vivo imaging of a tissue comprising:
(a) administering to a mammal a serine palmitoyltransferase specific compound, wherein the compound comprises a detectable label, and wherein the compound binds to mammalian cells which hyperproliferatively express serine palmitoyltransferase; and, (b) determining the location of the cells within a tissue of the mammal by imaging the detectable label.
- 4. The method of claim 2 further comprising the step of using the measured difference in the levels of serine palmitoyltransferase expressed by the first and second cells to detect, diagnose, diagnose the metastatic potential of, monitor the prognosis and progression of, or monitor the therapeutic efficacy of a treatment of a cancer.
- 5. The method of claim 4, wherein the cancer is selected from the group consisting of breast carcinoma, colonic carcinoma, carcinoid, gastric carcinoma, glioma, hepatoma, leiomyosarcoma, liver carcinoma, lung carcinoma, lymphoma, melanoma, mesothelioma, myeloma, ovarian carcinoma, pancreas carcinoma, prostate carcinoma, thyroid carcinoma, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, sarcoma, undifferentiated carcinoma, and leukemia.
- 6. The method of claim 2 further comprising the step of using the measured difference in levels of serine palmitoyltransferase expressed by the first and second cells to detect or diagnose the occurrence of vascular injury.
- 7. The method of claim 6 wherein the vascular injury is restenosis.
- 8. The method of claim 2 further comprising the step of using the measured difference in levels of serine palmitoyltransferase expressed by the first and second cells to detect or diagnose the occurrence of inflammation.
- 9. The method of claim 8 wherein the inflammation is the result of ulcerative colitis, inflammatory bowel syndrome, Crohn's Disease, rheumatoid arthritis, atherosclerosis, stroke, or asthma.
- 10. A method for screening a therapeutically effective compound that inhibits serine palmitoyltransferase comprising:
(a) contacting a serine palmitoyltransferase specific compound with a first mammalian cell which hyperproliferatively expresses serine palmitoyltransferase to form a first plurality of compound-serine palmitoyltransferase complexes; (b) contacting a potential serine palmitoyltransferase inhibitor compound with a second mammalian cell which hyperproliferatively expresses serine palmitoyltransferase to form a second plurality of compound-serine palmitoyltransferase complexes; (c) determining the levels of serine palmitoyltransferase expressed by the first and second cells by detecting the presence of the first and second plurality of compound-serine palmitoyltransferase complexes; and, (d) measuring the difference in the levels of serine palmitoyltransferase expressed by the first and second cells to determine whether the potential inhibitor compound inhibits serine palmitoyltransferase expression.
- 11. The method of claim 1, wherein the serine palmitoyltransferase specific compound is selected from the group consisting of a compound that binds to serine palmitoyltransferase, a monospecific antibody that binds to serine palmitoyltransferase, and a nucleic acid that will hybridize with serine palmitoyltransferase mRNA.
- 12. The method of claim 2, wherein the serine palmitoyltransferase specific compound is selected from the group consisting of a compound that binds to serine palmitoyltransferase, a monospecific antibody that binds to serine palmitoyltransferase, and a nucleic acid that will hybridize with serine palmitoyltransferase mRNA.
- 13. The method of claim 3, wherein the serine palmitoyltransferase specific compound is selected from the group consisting of a compound that binds to serine palmitoyltransferase, a monospecific antibody that binds to serine palmitoyltransferase, and a nucleic acid that will hybridize with serine palmitoyltransferase mRNA.
- 14. The method of claim 10, wherein the serine palmitoyltransferase specific compound is selected from the group consisting of a compound that binds to serine palmitoyltransferase, a monospecific antibody that binds to serine palmitoyltransferase, and a nucleic acid that will hybridize with serine palmitoyltransferase mRNA.
- 15. The method of claim 1 wherein the mammalian cells which express serine palmitoyltransferase are selected from the group consisting of adrenal cells, brain cells, breast cells, colon cells, epithelial cells, endothelial cells, heart cells, immunological cells, kidney cells, liver cells, lung cells, ovary cells, pancreas cells, prostate cells, skin cells, spleen cells, stomach cells, testis cells, thyroid cells, uterus cells and vascular cells.
- 16. The method of claim 15 wherein the epithelial cells are selected from the group consisting of endothelial cells, non-glial neuronal cells, colon cells, breast cells, the proximal tubules of the kidney, smooth muscle of the prostate, smooth muscle of the uterus and smooth muscle of the testis.
- 17. The method of claim 15 wherein the immunological cells are selected from the group consisting of polymorphonuclear leukocytes, monocytes, macrophages, epitheloid cells, giant cells, microglia, Kupffer cells and alveolar macrophages.
- 18. The method of claim 2 wherein the mammalian cells which basally express serine palmitoyltransferase are selected from the group consisting of adrenal cells, brain cells, breast cells, colon cells, epithelial cells, endothelial cells, heart cells, immunological cells, kidney cells, liver cells, lung cells, ovary cells, pancreas cells, prostate cells, skin cells, spleen cells, stomach cells, testis cells, thyroid cells, uterus cells, and vascular cells.
- 19. The method of claim 2 wherein the mammalian cells which hyperproliferatively express serine palmitoyltransferase are selected from the group consisting of epithelial cells, endothelial cells, cancer cells, immunological cells, and cells within a tumor microenvironment.
- 20. The method of claim 19, wherein the cancer cells are selected from the group consisting of breast carcinoma, colonic carcinoma, carcinoid, gastric carcinoma, glioma, hepatoma, leiomyosarcoma, liver carcinoma, lung carcinoma, lymphoma, melanoma, mesothelioma, myeloma, ovarian carcinoma, pancreas carcinoma, prostate carcinoma, thyroid carcinoma, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, sarcoma, undifferentiated carcinoma, and leukemia.
- 21. The method of claim 19, wherein the epithelial cells are selected from the group consisting of endothelial cells, non-glial neuronal cells, colon cells, breast cells, the proximal tubules of the kidney, smooth muscle of the prostate, smooth muscle of the uterus and smooth muscle of the testis.
- 22. The method of claim 19 wherein the immunological cells are selected from the group consisting of polymorphonuclear leukocytes, monocytes, macrophages, epitheloid cells, giant cells, microglia, Kupffer cells and alveolar macrophages.
- 23. The method of claim 19 wherein the cells within a tumor microenvironment are selected from the group consisting of stromal fibroblasts, stromal monocytes and myofibroblasts.
- 24. A method for treating a serine palmitoyltransferase mediated disorder in a subject in need thereof comprising administering a therapeutically effective amount of a pharmaceutical formulation of a serine palmitoyltransferase inhibitor compound to the subject; wherein, optionally, the serine palmitoyltransferase inhibitor compound is cytotoxic.
- 25. The method of claim 24, wherein the serine palmitoyltransferase inhibitor compound is a serine palmitoyltransferase specific compound.
- 26. The method of claim 24, wherein the serine palmitoyltransferase mediated disorder is selected from the group consisting of cancer, inflammation, and vascular injury.
- 27. The method of claim 26 wherein the cancer is selected from the group consisting of breast carcinoma, colonic carcinoma, carcinoid, gastric carcinoma, glioma, hepatoma, leiomyosarcoma, liver carcinoma, lung carcinoma, lymphoma, melanoma, mesothelioma, myeloma, ovarian carcinoma, pancreas carcinoma, prostate carcinoma, thyroid carcinoma, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, sarcoma, undifferentiated carcinoma, and leukemia.
- 28. The method of claim 26 wherein the inflammation is the result of ulcerative colitis, inflammatory bowel syndrome, Crohn's Disease, rheumatoid arthritis, atherosclerosis, stroke, or asthma.
- 29. The method of claim 26 wherein the vascular injury is the result of restenosis.
- 30. The method of claim 25 wherein the serine palmitoyltransferase specific compound is selected from the group consisting of a monospecific antibody optionally labeled with a cytotoxic agent, and a nucleic acid that will optionally hybridize to serine palmitoyltransferase mRNA.
- 31. The method of claim 24 wherein the pharmaceutical formulation is coated onto a balloon catheter or stent and released in a time-dependent manner.
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application claims benefit of provisional application Serial No. 60/277,252, filed Mar. 20, 2001, which is hereby incorporated by reference.
Provisional Applications (1)
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Number |
Date |
Country |
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60277252 |
Mar 2001 |
US |