RSPO3 binding agents and uses thereof
The present invention relates to RSPO-binding agents, particularly RSPO3-binding agents and methods of using the agents for treating diseases such as cancer. The present invention provides antibodies that specifically bind human RSPO3 proteins and modulate β-catenin activity. The present invention further provides methods of using agents that modulate the activity of RSPO3 proteins and inhibit tumor growth. Also described are methods of treating cancer comprising administering a therapeutically effect amount of an agent or antibody of the present invention to a patient having a tumor or cancer.
1. A method of treating cancer in a subject, wherein the method comprises administering to the subject a therapeutically effective amount of an antibody that specifically binds human R-spondin 3 (RSPO3), wherein the antibody comprises:
(a) a heavy chain CDR1 comprising KASGYTFTDYS (SEQ ID NO:9), KASGYTFTSYTF (SEQ ID NO:34), or DYSIH (SEQ ID NO:78), a heavy chain CDR2 comprising IYPSNGDS (SEQ ID NO:10) or YIYPSNGDSGYNQKFK (SEQ ID NO:79), and a heavy chain CDR3 comprising ATYFANYFDY (SEQ ID NO:11), ATYFANNFDY (SEQ ID NO:35), or TYFANNFD (SEQ ID NO:80); and
(b) a light chain CDR1 comprising QSVDYDGDSYM (SEQ ID NO:12) or KASQSVDYDGDSYMN (SEQ ID NO:81), a light chain CDR2 comprising AAS (SEQ ID NO:13) or AASNLES (SEQ ID NO:82), and a light chain CDR3 comprising QQSNEDPLT (SEQ ID NO:14) or QQSNEDPLTF (SEQ ID NO:83).
2. The method of claim 1 , wherein the antibody comprises:
(a) a heavy chain CDR1 comprising DYSIH (SEQ ID NO:78), a heavy chain CDR2 comprising YIYPSNGDSGYNQKFK (SEQ ID NO:79), and a heavy chain CDR3 comprising TYFANNFD (SEQ ID NO:80); and
(b) a light chain CDR1 comprising KASQSVDYDGDSYMN (SEQ ID NO:81), a light chain CDR2 comprising AASNLES (SEQ ID NO:82), and a light chain CDR3 comprising QQSNEDPLT (SEQ ID NO:14).
3. The method of claim 1 , wherein the antibody comprises:
(a) a heavy chain variable region having at least 90% sequence identity to SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:36, SEQ ID NO:37, SEQ ID NO:44, SEQ ID NO:45, or SEQ ID NO:62; and
(b) a light chain variable region having at least 90% sequence identity to SEQ ID NO:17, SEQ ID NO:72, or SEQ ID NO:86.
4. The method of claim 3 , wherein the antibody comprises:
(a) a heavy chain variable region comprising SEQ ID NO:15 and a light chain variable region comprising SEQ ID NO:17 or SEQ ID NO:72;
(b) a heavy chain variable region comprising SEQ ID NO:16 and a light chain variable region comprising SEQ ID NO:17 or SEQ ID NO:72;
(c) a heavy chain variable region comprising SEQ ID NO:36 and a light chain variable region comprising SEQ ID NO:17 or SEQ ID NO:72;
(d) a heavy chain variable region comprising SEQ ID NO:37 and a light chain variable region comprising SEQ ID NO:17 or SEQ ID NO:72;
(e) a heavy chain variable region comprising SEQ ID NO:44 and a light chain variable region comprising SEQ ID NO:17, SEQ ID NO:72, or SEQ ID NO:86;
(f) a heavy chain variable region comprising SEQ ID NO:45 and a light chain variable region comprising SEQ ID NO:17, SEQ ID NO:72, or SEQ ID NO:86; or
(g) a heavy chain variable region comprising SEQ ID NO:62 and a light chain variable region comprising SEQ ID NO:17, SEQ ID NO:72, or SEQ ID NO:86.
5. The method of claim 4 , wherein the antibody comprises a heavy chain variable region comprising SEQ ID NO:44 and a light chain variable region comprising SEQ ID NO:86.
6. The method of claim 1 , wherein the antibody is a recombinant antibody, a monoclonal antibody, a chimeric antibody, a bispecific antibody, a humanized antibody, an IgG1 antibody, an IgG2 antibody, or an antibody fragment comprising an antigen binding site.
7. The method of claim 1 , wherein the antibody comprises:
(a) a heavy chain sequence of SEQ ID NO:48 and a light chain sequence of SEQ ID NO:74 or SEQ ID NO:88;
(b) a heavy chain sequence of SEQ ID NO:64 and a light chain sequence of SEQ ID NO:74 or SEQ ID NO:88; or
(c) a heavy chain sequence of SEQ ID NO:69 and a light chain sequence of SEQ ID NO:74 or SEQ ID NO:88.
8. The method of claim 1 , wherein the antibody comprises a heavy chain variable region encoded by the plasmid deposited with ATCC as PTA-120420 and a light chain variable region encoded by the plasmid deposited with ATCC as PTA-120421.
9. The method of claim 1 , wherein the cancer is selected from the group consisting of colorectal cancer, ovarian cancer, pancreatic cancer, lung cancer, liver cancer, breast cancer, kidney cancer, prostate cancer, gastrointestinal cancer, melanoma, cervical cancer, bladder cancer, glioblastoma, and head and neck cancer.
10. The method of claim 9 , wherein the cancer is colorectal cancer.
11. The method of claim 1 , which further comprises administering at least one additional therapeutic agent.
12. The method of claim 11 , wherein the additional therapeutic agent is a chemotherapeutic agent.
13. The method of claim 12 , wherein the chemotherapeutic agent is irinotecan, fluorouracil, and/or folinic acid.
14. The method of claim 1 , wherein the cancer has an elevated expression level of RSPO3 as compared to a reference sample or a pre-determined level of RSPO3.
15. The method of claim 1 , wherein the cancer has a RSPO gene fusion.
16. A method of inhibiting growth of a tumor, wherein the method comprises contacting the tumor with an effective amount of an antibody that specifically binds human RSPO3, wherein the antibody comprises:
(a) a heavy chain CDR1 comprising KASGYTFTDYS (SEQ ID NO:9), KASGYTFTSYTF (SEQ ID NO:34), or DYSIH (SEQ ID NO:78), a heavy chain CDR2 comprising IYPSNGDS (SEQ ID NO: 10) or YIYPSNGDSGYNQKFK (SEQ ID NO:79), and a heavy chain CDR3 comprising ATYFANYFDY (SEQ ID NO:11), ATYFANNFDY (SEQ ID NO:35), or TYFANNFD (SEQ ID NO:80); and
(b) a light chain CDR1 comprising QSVDYDGDSYM (SEQ ID NO:12) or KASQSVDYDGDSYMN (SEQ ID NO:81), a light chain CDR2 comprising AAS (SEQ ID NO:13) or AASNLES (SEQ ID NO:82), and a light chain CDR3 comprising QQSNEDPLT (SEQ ID NO:14) or QQSNEDPLTF (SEQ ID NO:83).
17. A method of inhibiting growth of a tumor in a subject, wherein the method comprises administering to the subject a therapeutically effective amount of an antibody that specifically binds human RSPO3, wherein the antibody comprises:
(a) a heavy chain CDR1 comprising KASGYTFTDYS (SEQ ID NO:9), KASGYTFTSYTF (SEQ ID NO:34), or DYSIH (SEQ ID NO:78), a heavy chain CDR2 comprising IYPSNGDS (SEQ ID NO: 10) or YIYPSNGDSGYNQKFK (SEQ ID NO:79), and a heavy chain CDR3 comprising ATYFANYFDY (SEQ ID NO:11), ATYFANNFDY (SEQ ID NO:35), or TYFANNFD (SEQ ID NO:80); and
(b) a light chain CDR1 comprising QSVDYDGDSYM (SEQ ID NO:12) or KASQSVDYDGDSYMN (SEQ ID NO:81), a light chain CDR2 comprising AAS (SEQ ID NO:13) or AASNLES (SEQ ID NO:82), and a light chain CDR3 comprising QQSNEDPLT (SEQ ID NO:14) or QQSNEDPLTF (SEQ ID NO:83).
18. The method of claim 17 , wherein the antibody comprises:
(a) a heavy chain CDR1 comprising DYSIH (SEQ ID NO:78), a heavy chain CDR2 comprising YIYPSNGDSGYNQKFK (SEQ ID NO:79), and a heavy chain CDR3 comprising TYFANNFD (SEQ ID NO:80); and
(b) a light chain CDR1 comprising KASQSVDYDGDSYMN (SEQ ID NO:81), a light chain CDR2 comprising AASNLES (SEQ ID NO:82), and a light chain CDR3 comprising QQSNEDPLT (SEQ ID NO:14).
19. The method of claim 17 , wherein the tumor is selected from the group consisting of colorectal tumor, ovarian tumor, pancreatic tumor, lung tumor, liver tumor, breast tumor, kidney tumor, prostate tumor, gastrointestinal tumor, melanoma, cervical tumor, bladder tumor, glioblastoma, and head and neck tumor.
20. The method of claim 17 , wherein the tumor has an elevated expression level of RSPO3 as compared to a reference sample or a pre-determined level of RSPO3.
21. The method of claim 17 , wherein the tumor has a RSPO gene fusion.