Polypeptides antagonizing Wnt signaling in tumor cells
The invention provides LRP5-binding polypeptides, and more specifically LRP5-binding immunoglobulin single variable domain constructs which can inhibit Wnt signaling pathways. The invention also relates to specific sequences of such polypeptides, methods of their production, and methods of using them, including methods of treatment of diseases such as cancer.
1. A nucleic acid molecule encoding a biparatopic polypeptide comprising a first low-density lipoprotein receptor-like 5 protein (LRP5) epitope-binding domain, which binds a Wnt3a binding region of LRP5, wherein said first LRP5 epitope binding domain comprises a first immunoglobulin single variable domain (ISVD), and a second LRP5 epitope-binding domain, which binds a Wnt1 binding region of LRP5, wherein said second LRP5 epitope-binding domain comprises an ISVD, wherein said polypeptide comprising said first and said second ISVD are each selected from the group consisting of ISVDs (i) to (iv):
(i) an ISVD comprising the following complementarity-determining region (CDR) sequences:
(SEQ ID NO: 1)
CDR1: TYVMG,
(SEQ ID NO: 2)
CDR2: AISWSGGSTYYADSVKG,
(SEQ ID NO: 3)
CDR3: SRGTSTPSRASGVSRYDY,
(ii) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 4)
CDR1: RYAVA,
(SEQ ID NO: 5)
CDR2: AITWSSGRIDYADSVKG,
(SEQ ID NO: 6)
CDR3: DRRPRSTGRSGTGSPSTYDY,
(iii) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 7)
CDR1: IGAMG,
(SEQ ID NO: 8)
CDR2: AVSSGGSTYYVDSVKG,
(SEQ ID NO: 9)
CDR3: ETGPYGPPKRDY,
(iv) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 10)
CDR1: INAMG,
(SEQ ID NO: 8)
CDR2: AVSSGGSTYYVDSVKG,
(SEQ ID NO: 9)
CDR3: ETGPYGPPKRDY.
2. An expression vector comprising the nucleic acid molecule of claim 1 .
3. A host cell comprising an expression vector according to claim 2 .
4. A method of manufacturing a bipartopic polypeptide comprising the steps of:
a. culturing a host cell according to claim 3 under conditions that allow expression of the polypeptide; and
b. recovering the polypeptide,
wherein the polypeptide comprising said first and second ISVD are each selected from the group consisting of ISVDs (i) to (iv):
(i) an ISVD comprising the following complementarity-determining region (CDR) sequences:
(SEQ ID NO: 1)
CDR1: TYVMG,
(SEQ ID NO: 2)
CDR2: AISWSGGSTYYADSVKG,
(SEQ ID NO: 3)
CDR3: SRGTSTPSRASGVSRYDY;
(ii) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 4)
CDR1: RYAVA,
(SEQ ID NO: 5)
CDR2: AITWSSGRIDYADSVKG,
(SEQ ID NO: 6)
CDR3: DRRPRSTGRSGTGSPSTYDY;
(iii) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 7)
CDR1: IGAMG,
(SEQ ID NO: 8)
CDR2: AVSSGGSTYYVDSVKG,
(SEQ ID NO: 9)
CDR3: ETGPYGPPKRDY;
(iv) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 10)
CDR1: INAMG,
(SEQ ID NO: 8)
CDR2: AVSSGGSTYYVDSVKG,
(SEQ ID NO: 9)
CDR3: ETGPYGPPKRDY.
5. A method for the inhibition of tumor growth in a human being or an animal in need thereof comprising administrating a therapeutic agent comprising a biparatopic polypeptide comprising a first low-density lipoprotein receptor-like 5 protein (LRP5) epitope-binding domain, which binds a Wnt3a binding region of LRP5, wherein said first LRP5 epitope binding domain comprises a first immunoglobulin single variable domain (ISVD), and a second LRP5 epitope-binding domain, which binds a Wnt1 binding region of LRP5, wherein said second LRP5 epitope-binding domain comprises an ISVD, wherein said polypeptide comprising said first and said second ISVD are each selected from the group consisting of ISVDs (i) to (iv):
(i) an ISVD comprising the following complementarity-determining region (CDR) sequences:
(SEQ ID NO: 1)
CDR1: TYVMG,
(SEQ ID NO: 2)
CDR2: AISWSGGSTYYADSVKG,
(SEQ ID NO: 3)
CDR3: SRGTSTPSRASGVSRYDY,
(ii) an ISVD comprising the following CDR sequences:
CDR1:
(SEQ ID NO: 4)
RYAVA,
CDR2:
(SEQ ID NO: 5)
AITWSSGRIDYADSVKG,
CDR3:
(SEQ ID NO: 6)
DRRPRSTGRSGTGSPSTYDY,
(iii) an ISVD comprising the following CDR sequences:
(SEQ ID NO: 7)
CDR1: IGAMG,
(SEQ ID NO: 8)
CDR2: AVSSGGSTYYVDSVKG,
(SEQ ID NO: 9)
CDR3: ETGPYGPPKRDY,
and
(iv) an ISVD comprising the following CDR sequences:
CDR1:
(SEQ ID NO: 10)
INAMG,
CDR2:
(SEQ ID NO: 8)
AVSSGGSTYYVDSVKG,
CDR3:
(SEQ ID NO: 9)
ETGPYGPPKRDY.
6. The method of claim 5 , wherein said tumor growth is for a cancer selected from the group consisting of breast cancer, lung cancer, non-small-cell lung carcinoma (NSCLC), pancreatic cancer, colorectal cancer, sarcomas, ovarian cancer and hepatocellular carcinoma.
7. The method according to claim 6 , wherein breast cancer is a triple negative breast cancer (TNBC).
8. The method according to claim 5 , wherein the biparatopic polypeptide is administered in combination with a second therapeutic agent selected from the group consisting of an angiogenesis inhibitor, a signal transduction pathway inhibitor, an EGFR inhibitor, an immune modulator, an immune checkpoint inhibitor, and a hormonal therapy agent.