Novel strategies to augment genetically delivered immunotoxin molecular therapy for cancer therapy.

Published

Journal Article

Immunotoxin therapy is a promising molecular cancer treatment strategy. Its main advantage is seletive cytotoxicity towards tumor cells and minimal toxicity in normal tissues. However, a short half-life and rapid clearance severely hampers its clinical application. We report here a novel genetic approach in which a recombinant adenovirus vector was used to deliver an immunotoxin gene e23(scFv)-PE40 targeted to the oncogene c-erbB-2 (also known as Her2/neu). This vector, when combined with a low dose of a conditionally replicative adenovirus vector (CRAd), has enhanced tumor-killing ability either alone or in combination with the chemotherapeutic agent etoposide. Our data show that low-dose CRAd facilitated the replication of replication-deficient Ad-e23(scFv)-PE40 up to 6-20 times and the transcription of e23(scFv)-PE40 gene up to 12 times. Moreover, etoposide increased the e23(scFv)-PE40 transcription up to 8.5 times. Furthermore, we show that systemic application of Ad-e23(scFv)-PE40 and enhanced expression of the immunotoxin gene was well tolerated as determined by serum biochemical markers and histological examination of most vital organs. Taken together, our data support a novel genetic immunotoxin delivery approach that may yield enhanced efficacy against a variety of Her2/neu-expressing tumors.

Full Text

Duke Authors

Cited Authors

  • Liu, X; Wu, J; Zhang, S; Li, C; Huang, Q

Published Date

  • November 2009

Published In

Volume / Issue

  • 16 / 11

Start / End Page

  • 861 - 872

PubMed ID

  • 19461676

Pubmed Central ID

  • 19461676

Electronic International Standard Serial Number (EISSN)

  • 1476-5500

Digital Object Identifier (DOI)

  • 10.1038/cgt.2009.30

Language

  • eng

Conference Location

  • England