Methods and compositions for inhibiting the growth and/or proliferation of myc-driven tumor cells
US-2018110788-A1 · Apr 26, 2018 · US
US10188630B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10188630-B2 |
| Application number | US-201715712849-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 22, 2017 |
| Priority date | Apr 6, 2010 |
| Publication date | Jan 29, 2019 |
| Grant date | Jan 29, 2019 |
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In one aspect, the invention provides a method for inhibiting the growth and/or proliferation of a myc-driven tumor cell comprising the step of contacting the tumor cells with a CSNK1ε inhibitor. In another aspect, the invention provides a method of treating a subject suffering from a tumor comprising myc-driven tumor cells, comprising administering to the subject an amount of a composition comprising a CSNK1ε inhibitor effective to inhibit the growth and/or proliferation of the tumor cells.
Opening claim text (preview).
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows: 1. A method of treating a subject having a tumor comprising tumor cells of neural origin that overexpress Myc, comprising: determining that the tumor comprises tumor cells that overexpress Myc; and then administering to the subject an amount of a composition comprising a CSNK1ε inhibitor effective to inhibit the growth and/or proliferation of the tumor cells. 2. The method of claim 1 , wherein the tumor is a primary neuroblastoma tumor, a metastatic neuroblastoma tumor, or a brain tumor. 3. The method of claim 1 , wherein the tumor is a primary neuroblastoma tumor or a metastatic neuroblastoma tumor. 4. The method of claim 1 , wherein the subject is further provided one or more additional anti-cancer therapies. 5. The method of claim 4 , wherein the additional anti-cancer therapy comprises chemotherapy. 6. The method of claim 5 , wherein the tumor cells that overexpresses Myc are resistant to cisplatin, and the CSNK1ε inhibitor renders the cell susceptible to cisplatin. 7. The method of claim 1 , wherein the CSNK1ε inhibitor is a small molecule inhibitor. 8. The method of claim 7 , wherein the CSNK1ε inhibitor is selected from the group consisting of IC261, PF-4800567, and PF-670462. 9. The method of claim 1 , wherein the Myc is c-Myc or MycN.
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