Methods, compositions and screens for therapeutics for the treatment of synovial sarcoma
Methods and compositions are provided for treating human synovial sarcoma (SS). Also provided are screens to identify therapeutics for the treatment of synovial sarcoma. These methods, compositions, and screens are based on the discovery that promoting the assembly of wild type BAF (also called mSWI/SNF) complexes in SS cells by increasing levels of wild type SS18 and/or decreasing levels of SS18-SSX fusion protein leads to the cessation of proliferation of malignant cells in synovial sarcoma.
1. A method of promoting the assembly of wild-type BAF complexes in a cell, the method comprising:
contacting a cell comprising a mutant BAF complex with an effective amount of a wild-type BAF complex promoting agent to promote the assembly of wild-type BAF complexes in the cell, wherein the agent increases amounts in the cell of one or more of: wild type SS18 polypeptide, an active fragment of the wild type SS18 polypeptide, wild-type BAF47 polypeptide, and an active fragment of the wild-type BAF47 polypeptide.
2. The method according to claim 1 , wherein the mutant BAF complex comprises a SS18-SSX fusion polypeptide.
3. The method according to claim 2 , wherein the wild-type BAF complex promoting agent displaces the SS18-SSX fusion polypeptide from the mutant BAF complex.
4. The method according to claim 1 , wherein the wild-type BAF complex promoting agent increases the amount of wild type SS18 polypeptide in the cell.
5. The method according to claim 1 , wherein the cell is a human cell.
6. A method for treating human synovial sarcoma (SS) in an individual, the method comprising:
administering to an individual who has SS, an effective amount of a wild-type BAF complex promoting agent to promote the assembly of wild-type BAF complexes in SS cells comprising a mutant BAF complex and treat the individual for SS, wherein the agent increases amounts in SS cells of one or more of: wild type SS18 polypeptide, an active fragment of the wild type SS18 polypeptide, wild-type BAF47 polypeptide, and an active fragment of the wild-type BAF47 polypeptide.
7. The method according to claim 6 , wherein the mutant BAF complex comprises a SS18-SSX fusion polypeptide.
8. The method according to claim 7 , wherein the wild-type BAF complex promoting agent displaces the SS18-SSX fusion polypeptide from the mutant BAF complex.
9. The method according to claim 6 , wherein the wild-type BAF complex promoting agent increases the amount of wild type SS18 polypeptide in the cell.
10. The method according to claim 6 , further comprising administering chemotherapy to the individual.
11. The method according to claim 6 , further comprising administering radiotherapy to the individual.