| CPC A61K 31/337 (2013.01) [A61K 33/24 (2013.01); A61K 39/0005 (2013.01); A61K 45/06 (2013.01); A61K 47/64 (2017.08); A61K 49/0032 (2013.01); A61K 49/0056 (2013.01); A61K 49/0058 (2013.01); A61K 49/14 (2013.01); A61K 49/16 (2013.01); A61K 49/1866 (2013.01); A61K 51/1093 (2013.01); B82Y 5/00 (2013.01); C07K 16/28 (2013.01); G01N 33/57415 (2013.01); G01N 33/57434 (2013.01); G01N 33/57449 (2013.01); G01N 33/57492 (2013.01); G01N 33/6872 (2013.01); A61K 33/242 (2019.01); G01N 2333/705 (2013.01)] | 8 Claims |
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1. A method for the treatment of cancer by delivering a biomolecule to a cell expressing Transient Receptor Potential Vanilloid 6 (TRPV6), comprising contacting the cell in vivo with a compound comprising a TRPV6-binding peptide conjugated to the biomolecule, wherein the biomolecule is an anti-cancer agent, and wherein the TRPV6-binding peptide:
a) comprises from 9 to 27 contiguous C-terminal amino acids of SEQ ID NO:1;
b) has an amino acid sequence with at least 90% identity to HPSKVDLPR (SEQ ID NO: 3);
c) has an amino acid sequence with at least 90% identity to KEFLHPSKVDLPR (SEQ ID NO: 4); or
d) has an amino acid sequence with at least 90% identity to
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