NOTUM PROTEIN MODULATORS AND METHODS OF USE
Novel modulators, including antibodies and derivatives thereof, and methods of using such modulators to treat hyperproliferative disorders are provided.
1 - 101 . (canceled)
102 . An isolated anti-Notum antibody which competes with hSC2.D2.2 antibody for binding to Notum.
103 . The anti-Notum antibody of claim 102 , comprising a heavy chain and a light chain; wherein
the heavy chain comprises CDR1 comprising the amino acid sequence of SEQ ID NO:122, CDR2 comprising the amino acid sequence of SEQ ID NO:160, and CDR3 comprising the amino acid sequence of SEQ ID NO:198; and
the light chain comprises CDR1 comprising the amino acid sequence of SEQ ID NO:236, CDR2 comprising the amino acid sequence of SEQ ID NO:274, and CDR3 comprising the amino acid sequence of SEQ ID NO:312.
104 . The anti-Notum antibody of claim 103 , wherein the heavy chain comprises a variable region comprising the amino acid sequence of SEQ ID NO:331 and the light chain comprises a variable region comprising the amino acid sequence of SEQ ID NO:332.
105 . The anti-Notum antibody of claim 103 , wherein the antibody is hSC2.D2.2 antibody.
106 . An isolated anti-Notum antibody comprising CDR1, CDR2, and CDR3 of the heavy chain and CDR1, CDR2, and CDR3 of the light chain of an antibody selected from SC2.A1 antibody, SC2.A3 antibody, SC2.A6 antibody, SC2.A8 antibody, SC2.A11 antibody. SC2.A12 antibody, SC2.A13 antibody, SC2.A101 antibody, SC2.A109 antibody, SC2.A113 antibody, SC2.A106 antibody, SC2.A122 antibody, SC2.10E11 antibody, SC2.9E7 antibody, SC2.A118 antibody, SC2.A126 antibody, SC2.5C4 antibody, SC2.A110 antibody, SC2.D1 antibody, SC2.D3 antibody, SC2.D4 antibody, SC2.D7 antibody, SC2.D12 antibody, SC2.D14 antibody, SC2.D15 antibody, SC2.D16 antibody, SC2.D19 antibody, SC2.D22 antibody, SC2.D23 antibody, SC2.D27 antibody, SC2.D28 antibody, SC2.D30 antibody, SC2.D41 antibody, SC2.D45 antibody, SC2.D46 antibody, SC2.D47 antibody, and SC2.D57 antibody.
107 . The antibody of any one of claims 102 to 106 , wherein the antibody is conjugated to an anti-cancer agent.
108 . The antibody of any one of claims 102 to 107 , wherein the antibody is a chimeric antibody or a humanized antibody.
109 . A method of treating a patient having at least one neoplastic disorder selected from adrenal cancer, bladder cancer, cervical cancer, endometrial cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, colorectal cancer, pancreatic cancer, prostate cancer, breast cancer, and cancer metastasis, comprising administering a therapeutically effective amount of an antibody of any one of claims 102 to 108 to the patient.
110 . The method of claim 109 wherein the patient has a solid tumor exhibiting at least one mutation selected from a KRAS mutation, an APC mutation, and a CTNNB1 mutation.
111 . The method of claim 109 or claim 110 , wherein the treatment reduces the frequency of tumor initiating cells in the patient, wherein the reduction in frequency is determined: using flow cytometric analysis of tumor cell surface markers known to enrich for tumor initiating cells; using immunohistochemical detection of tumor cell surface markers known to enrich for tumor initiating cells; using in vitro or in vivo limiting dilution analysis; using in vivo limiting dilution analysis comprising transplant of live human tumor cells into immunocompromised mice; using in vivo limiting dilution analysis comprising quantification of tumor initiating cell frequency using Poisson distribution statistics; using in vitro limiting dilution analysis comprising limiting dilution deposition of live human tumor cells into in vitro colony supporting conditions; or using in vitro limiting dilution analysis comprises quantification of tumor initiating cell frequency using Poisson distribution statistics.
112 . A composition comprising an antibody of any one of claims 102 to 108 and a pharmaceutically acceptable carrier.
113 . An isolated composition comprising a first polynucleotide and a second polynucleotide, wherein the first polynucleotide encodes a heavy chain and the second polynucleotide encodes a light chain, and wherein the first and second polynucleotides encode an antibody of any one of claims 102 to 108 .
114 . An isolated host cell comprising a first polynucleotide and a second polynucleotide, wherein the first polynucleotide encodes a heavy chain and the second polynucleotide encodes a light chain, and wherein the first and second polynucleotides encode an antibody of any one of claims 102 to 108 .
115 . A method of diagnosing a hyperproliferative disorder in a patient comprising:
a. obtaining a tissue sample from the patient;
b. contacting the tissue sample with an anti-Notum antibody of any one of claims 102 to 108 ; and
c. detecting or quantifying the anti-Notum antibody associated with the sample.