Targeting the cancer stroma with a fibroblast activation protein-activated promelittin protoxin

AM LeBeau, WN Brennen, S Aggarwal… - Molecular cancer …, 2009 - AACR
AM LeBeau, WN Brennen, S Aggarwal, SR Denmeade
Molecular cancer therapeutics, 2009AACR
Abstract Fibroblast-Activation Protein-α (FAP) is a membrane-bound serine protease that is
expressed on the surface of reactive stromal fibroblasts present within the majority of human
epithelial tumors but is not expressed by normal tissues. FAP is a postprolyl peptidase that
differs from other dipeptidyl prolyl peptidases such as diprolylpeptidase 4 in that it also has
gelatinase and collagenase endopeptidase activity. Therefore, FAP represents a potential
pan-tumor target whose enzymatic activity can be exploited for the intratumoral activation of …
Abstract
Fibroblast-Activation Protein-α (FAP) is a membrane-bound serine protease that is expressed on the surface of reactive stromal fibroblasts present within the majority of human epithelial tumors but is not expressed by normal tissues. FAP is a postprolyl peptidase that differs from other dipeptidyl prolyl peptidases such as diprolylpeptidase 4 in that it also has gelatinase and collagenase endopeptidase activity. Therefore, FAP represents a potential pan-tumor target whose enzymatic activity can be exploited for the intratumoral activation of prodrugs and protoxins. To evaluate FAP as a tumor-specific target, putative FAP-selective peptide protoxins were constructed through modification of the prodomain of melittin, a 26 amino acid amphipathic cytolytic peptide that is the main toxic component in the venom of the common European honeybee Apis milefera. Melittin is synthesized as promelittin, containing a 22 amino acid NH2-terminal prodomain rich in the amino acids proline and alanine. In this study, peptides containing truncated melittin prodomain sequences were tested on erythrocytes to determine the optimal prodomain length for inhibiting cytolytic activity. Once optimized, modified promelittin peptides were generated in which previously identified FAP substrate sequences were introduced into the prodomain. Peptide protoxins were identified that were efficiently activated by FAP and selectively toxic to FAP-expressing cell lines with an IC50 value in the low micromolar range that is similar to melittin. Intratumoral injection of an FAP-activated protoxin produced significant lysis and growth inhibition of human breast and prostate cancer xenografts with minimal toxicity to the host animal. [Mol Cancer Ther 2009;8(5):1378–86]
AACR