ANTIBODY MEDIATED GENE DELIVERY OF THE TUMOR SUPPRESSOR PROTEIN p53
UCLA Technology Available For Licensing

BACKGROUND:  p53 plays a pivotal role towards inhibition of tumor progression, survival, and metastasis. As such, p53 has been a central target in tumor therapy and in particular, gene therapy targeting cancer. Recent efforts in utilizing p53 as a gene therapy show varying efficacies. The primary cause for these inconsistencies appears to be the inherit obstacles which gene therapy must overcome. Current approaches in gene therapy are hampered by inefficient delivery, toxicity concerns, immunogenicity, proper gene function, and limited expression of the gene delivered. Due to its potent tumor suppressing capacity, however, gene therapy with p53 continues to be one of the more sought after tumor therapies.

INNOVATION:  UCLA Researchers have developed a novel method to deliver functional p53 to tumor cells by fusion of p53 to the Fv peptide of a murine antibody (Fv-p53). This approach allows for delivery of p53 to tumor cells both in vitro and in vivo. Furthermore, Fv-p53 induces apoptosis in tumor cells in vitro and prevents metastasis of colon cancer in vivo. Therefore, Fv-p53 represents a novel protein (gene) therapy in cancer treatment.

POTENTIAL APPLICATIONS 

ADVANTAGES

Related Papers (Selected)

Reference: UCLA Case No. 2007-250

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availability, please contact the following UCLA office:

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email: ncd@research.ucla.edu
NCD URL:   http://www.research.ucla.edu/tech/ucla07-250.htm

Lead Inventor: Richard Weisbart

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http://www.research.ucla.edu/oipa/industry

Copyright © 2007 The Regents of the University of California.

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