Claims for Patent: 9,333,217

Summary for Patent: 9,333,217

Title:	Inhibitors of human EZH2, and methods of use thereof
Abstract:	The invention relates to inhibition of wild-type and certain mutant forms of human histone methyltransferase EZH2, the catalytic subunit of the PRC2 complex which catalyzes the mono- through tri-methylation of lysine 27 on histone H3 (H3-K27). In one embodiment the inhibition is selective for the mutant form of the EZH2, such that trimethylation of H3-K27, which is associated with certain cancers, is inhibited. The methods can be used to treat cancers including follicular lymphoma and diffuse large B-cell lymphoma (DLBCL). Also provided are methods for identifying small molecule selective inhibitors of the mutant forms of EZH2 and also methods for determining responsiveness to an EZH2 inhibitor in a subject.
Inventor(s):	Copeland; Robert A. (Lexington, MA), Richon; Victoria M. (Wellesley, MA), Scott; Margaret D. (Beverly, MA), Sneeringer; Christopher J. (San Francisco, CA), Kuntz; Kevin W. (Woburn, MA), Knutson; Sarah K. (Cambridge, MA), Pollock; Roy M. (Medford, MA)
Assignee:	Epizyme, Inc. (Cambridge, MA)
Application Number:	14/540,977
Patent Claims:	1. A method for treating cancer in a subject, comprising (i) contacting a biological sample obtained from the subject with at least one antibody that binds specifically to a mutant Enhancer of Zeste Homolog 2 (EZH2) comprising a mutation at position Y641 in the EZH2 of SEQ ID NO: 1, wherein the mutation increases EZH2 trimethylation of Lys27 of histone H3 (H3-K27), wherein the mutation at position Y641 in the EZH2 of SEQ ID NO: 1 is selected from the group consisting of Y641F, Y641H, Y641N and Y641S, and wherein the at least one antibody and the mutant form a complex; (ii) detecting the presence of the mutation at position Y641 in the EZH2 of SEQ ID NO: 1 by detecting the complex formed in step (i); and (iii) administering a therapeutically effective amount of an inhibitor of EZH2 to the subject if the mutation at position Y641 in the EZH2 of SEQ ID NO: 1 is detected in the biological sample obtained from the subject, wherein the EZH2 inhibitor inhibits the conversion of H3-K27 to trimethylated H3-K27. 2. The method of claim 1, wherein said subject has a cancer selected from leukemia, melanoma, and lymphoma, or is at risk of developing a cancer selected from leukemia, melanoma, and lymphoma. 3. The method of claim 2, wherein said lymphoma is selected from the group consisting of Non-Hodgkin's lymphoma, follicular lymphoma and diffuse large B-cell lymphoma (DLBCL) of germinal center B cell-like (GCB) subtype. 4. The method of claim 1, wherein inhibition of EZH2 is selective inhibition. 5. The method claim 1, wherein the inhibitor of EZH2 is a small molecule. 6. The method of claim 1, wherein the cancer is lymphoma.