Inhibitors of aortic carboxypeptidase-like protein (ACLP)
The present invention generally relates to the field of treatment of fibroproliferative diseases and disorders and cancer. Embodiments of the present invention generally relate to compostions, methods and kits comprising an inhibitor of a portion of the N-terminal pro-fibrotic domain (PFD) of Aortic Carboxypeptidase-Like Protein (ACLP), and in some embodiments, in combination with an inhibitor of the discoidin (DS) domain of ACLP, for use in methods for the treatment of fibroproliferative diseases and cancer, and inhibition of ACLP-mediated activation of a member of the TGFβ receptor superfamily.
1. An admixture comprising:
a) a first peptide that comprises at least 5 consecutive amino acids of the amino acid sequence of SEQ ID NO: 3 or SEQ ID NO: 4 and has at least 85% sequence identity to the amino acid sequence of SEQ ID NO: 3 or SEQ ID NO: 4; and
b) a second peptide that comprises at least 5 consecutive amino acid residues of amino acids 384-539 of SEQ ID NO: 1.
2. The admixture of claim 1 , wherein the first peptide, or second peptide, or both are fused to a Fc, wherein the Fc comprises the amino acid sequence of SEQ ID NO: 48 or a Fc variant having at least 85% sequence identity to SEQ ID NO: 48.
3. The admixture of claim 1 , wherein first peptide comprises at least 5 consecutive amino acids of KEKPPKATKKPKEKPPKATKKPKEKPPKATKKPKEKPPKATKKP (SEQ ID NO: 4).
4. The admixture of claim 1 , wherein the second peptide comprises:
(i) at least 5 consecutive amino acids from at least one loop region within amino acids 384-539 of SEQ ID NO: 1, wherein the loop region is selected from: MLRHGLG (SEQ ID NO: 12), QTGATEDDYYDGA (SEQ ID NO: 13), DARTQ (SEQ ID NO: 14) and RDSSIHDD (SEQ ID NO: 15); or
(ii) a peptide selected from the group consisting of: MLRHGLG (SEQ ID NO: 12); MLRHGLGA (SEQ ID NO: 16); MLRHGLGAQ (SEQ ID NO: 17); SMLRHGLG (SEQ ID NO: 18); SMLRHGLG (SEQ ID NO: 19); SMLRHGLGA (SEQ ID NO: 20); SMLRHGLGAQ (SEQ ID NO: 21); SSMLRHGLGA (SEQ ID NO: 22); SSMLRHGLGAQ (SEQ ID NO: 23); QTGATEDDYYDGA (SEQ ID NO: 13); QTGATEDDYYDGAW (SEQ ID NO: 24); QTGATEDDYYDGAWC (SEQ ID NO: 25); MQTGATEDDYYDGA (SEQ ID NO: 26); NMQTGATEDDYYDGA (SEQ ID NO: 27); MQTGATEDDYYDGAW (SEQ ID NO: 28); MQTGATEDDYYDGAWC (SEQ ID NO: 29); NMQTGATEDDYYDGAW (SEQ ID NO: 30); NMQTGATEDDYYDGAWC (SEQ ID NO: 31); DARTQ (SEQ ID NO: 14); DARTQW (SEQ ID NO: 32); DARTQWI (SEQ ID NO: 33); DDARTQ (SEQ ID NO: 34); EDDARTQ (SEQ ID NO: 35); DDARTQW (SEQ ID NO: 36); DDARTQWI (SEQ ID NO: 37); EDDARTQW (SEQ ID NO: 38); EDDARTQWI (SEQ ID NO: 39); RDSSIHDD (SEQ ID NO: 15); RDSSIHDDF (SEQ ID NO: 40); RDSSIHDDFV (SEQ ID NO: 41); GRDSSIHDD (SEQ ID NO: 42); QGRDSSIHDD (SEQ ID NO: 43); GRDSSIHDDF (SEQ ID NO: 44); GRDSSIHDDFV (SEQ ID NO: 45); QGRDSSIHDDF (SEQ ID NO: 46); and QGRDSSIHDDFV (SEQ ID NO: 47).
5. The admixture of claim 1 , for use in a method to treat a fibroproliferative disease or a solid cancer with a fibrotic core.
6. A kit comprising:
a first container comprising a first peptide that comprises at least 5 consecutive amino acids of the amino acid sequence of SEQ ID NO: 3 or SEQ ID NO: 4 and has at least 85% sequence identity to the amino acid sequence of SEQ ID NO: 3 or SEQ ID NO: 4, and
a second container comprising a second peptide comprising at least 5 consecutive amino acid residues of amino acids 384-539 of SEQ ID NO: 1.
7. The kit of claim 6 , wherein the first peptide comprises at least 5 consecutive amino acids of KEKPPKATKKPKEKPPKATKKPKEKPPKATKKPKEKPPKATKKP (SEQ ID NO: 4), and can be optionally fused to a Fc comprising the amino acid sequence of SEQ ID NO: 48 or a fragment of SEQ ID NO: 48.
8. The kit of claim 6 , wherein the second peptide is selected from the group consisting of:
(i) at least 5 consecutive amino acids from at least one loop region within amino acids 384-539 of SEQ ID NO: 1, wherein the loop region is selected from: MLRHGLG (SEQ ID NO: 12), QTGATEDDYYDGA (SEQ ID NO: 13), DARTQ (SEQ ID NO: 14) and RDSSIHDD (SEQ ID NO: 15); and
(ii) a peptide selected from the group consisting of: MLRHGLG (SEQ ID NO: 12); MLRHGLGA (SEQ ID NO: 16); MLRHGLGAQ (SEQ ID NO: 17); SMLRHGLG (SEQ ID NO: 18); SMLRHGLG (SEQ ID NO: 19); SMLRHGLGA (SEQ ID NO: 20); SMLRHGLGAQ (SEQ ID NO: 21); SSMLRHGLGA (SEQ ID NO: 22); SSMLRHGLGAQ (SEQ ID NO: 23); QTGATEDDYYDGA (SEQ ID NO: 13); QTGATEDDYYDGAW (SEQ ID NO: 24); QTGATEDDYYDGAWC (SEQ ID NO: 25); MQTGATEDDYYDGA (SEQ ID NO: 26); NMQTGATEDDYYDGA (SEQ ID NO: 27); MQTGATEDDYYDGAW (SEQ ID NO: 28); MQTGATEDDYYDGAWC (SEQ ID NO: 29); NMQTGATEDDYYDGAW (SEQ ID NO: 30); NMQTGATEDDYYDGAWC (SEQ ID NO: 31); DARTQ (SEQ ID NO: 14); DARTQW (SEQ ID NO: 32); DARTQWI (SEQ ID NO: 33); DDARTQ (SEQ ID NO: 34); EDDARTQ (SEQ ID NO: 35); DDARTQW (SEQ ID NO: 36); DDARTQWI (SEQ ID NO: 37); EDDARTQW (SEQ ID NO: 38); EDDARTQWI (SEQ ID NO: 39); RDSSIHDD (SEQ ID NO: 15); RDSSIHDDF (SEQ ID NO: 40); RDSSIHDDFV (SEQ ID NO: 41); GRDSSIHDD (SEQ ID NO: 42); QGRDSSIHDD (SEQ ID NO: 43); GRDSSIHDDF (SEQ ID NO: 44); GRDSSIHDDFV (SEQ ID NO: 45); QGRDSSIHDDF (SEQ ID NO: 46) and QGRDSSIHDDFV (SEQ ID NO: 47),
wherein the second peptide can be optionally fused to a Fc comprising the amino acid sequence of SEQ ID NO: 48 or a fragment of SEQ ID NO: 48.
9. The kit of claim 6 , wherein the first peptide or the second peptide, or both is at least one of:
(a) in a lyophilized form;
(b) in a form comprising a detectable label; or
(c) is conjugated to an anti-cancer agent.