Carcinoma homing peptide (CHP), its analogs, and methods of using
A mini-peptide and its analogs have been found to target gene products to tumors. The peptide, named Carcinoma Homing Peptide (CHP), increased the tumor accumulation of the reporter gene products in five independent tumor models, including one human xenogeneic model. A CHP-IL-12 fusion gene was also developed using CHP and the p40 subunit of IL-12. The product from CHP-IL-12 fusion gene therapy increased accumulation of IL-12 in the tumor environment. In three tumor models, CHP-IL-12 gene therapy inhibited distal tumor growth. In a spontaneous lung metastasis model, inhibition of metastatic tumor growth was improved compared to wild-type IL-12 gene therapy, and in a squamous cell carcinoma model, toxic liver lesions were reduced. The receptor for CHP was identified as vimentin. CHP can be used to improve the efficacy and safety of targeted cancer treatments.
1. A tumor-targeting conjugate comprising an anti-tumor therapeutic agent conjugated to a carcinoma homing peptide (CHP) wherein the CHP is SEO ID NO:1,
wherein the anti-tumor therapeutic agent is interleukin 12,
wherein the carcinoma homing peptide is directly coupled to the p40 subunit of interleukin 12, and
wherein the amino acid sequence of the conjugate is SEQ ID NO:3.
2. The conjugate as in claim 1 , wherein the conjugate selectively binds vimentin on the surface of a tumor cell.
3. A viral or non-viral vector comprising a composition encoding the conjugate of claim 1 .
4. The vector as in claim 3 , wherein the composition is the DNA sequence of SEQ ID NO:4.
5. A plasmid construct comprising a composition encoding the conjugate of claim 1 .
6. The plasmid as in claim 5 , wherein the composition is the DNA sequence of SEQ ID NO:4.
7. A method to decrease the size of a mammalian tumor, said method comprising administering to the mammal the conjugate of claim 1 wherein the mammalian tumor is selected from one or more tumors of the group consisting of breast adenocarcinoma, squamous cell carcinoma, and colon carcinoma.
8. A method to inhibit growth of a mammalian tumor, said method comprising administering to the mammal the conjugate of claim 1 wherein the mammalian tumor is selected from one or more tumors of the group consisting of breast adenocarcinoma, squamous cell carcinoma, and colon carcinoma.
9. A method to inhibit growth of a mammalian tumor, said method comprising administering to the mammal the vector of claim 3 wherein the mammalian tumor is selected from one or more tumors of the group consisting of breast adenocarcinoma, squamous cell carcinoma, and colon carcinoma.
10. The method of or claim 9 , wherein the composition is the DNA sequence of SEQ ID NO:4.
11. A method to inhibit growth of a mammalian tumor, said method comprising administering to the mammal the plasmid of claim 5 wherein the mammalian tumor is selected from one or more tumors of the group consisting of breast adenocarcinoma, squamous cell carcinoma, and colon carcinoma.
12. The method of claim 11 , wherein the composition is the DNA sequence of SEQ ID NO:4.