In vivo studies of adenovirus-based p53 gene therapy for ovarian cancer

Vivian E. Von Gruenigen, Joseph T. Santoso, Robert L. Coleman, Carolyn Y. Muller, David Scott Miller, J. Michael Mathis

Research output: Contribution to journalArticlepeer-review

34 Scopus citations


Objectives. To test the safety, efficacy, and toxicity of gene therapy using wild-type p53-expressing adenovirus (Ad-CMV-p53) in a nude mouse model with intraperitoneal (ip) 2774 human ovarian cancer cell line that contains a p53 mutation. Study design. An initial study of adenovirus tolerance was determined in nude mice by a single ip injection of increasing doses of Ad- CMV-p53. Nude mice were implanted with an LD100 dose of 1 x 107 cells. To study the efficacy and specificity of Ad-CMV-p53 treatment, the mice received treatment with different adenovirus constructs. One group received Ad-CMV- p53 and another group received a control adenovirus construct, Ad-CMV-βgal. To study the treatment response to Ad-CMV-p53, the mice were divided into groups and received various treatment schedules of 1 x 108 pfu of Ad-CMV- p53. Results. The mice tolerated Ad-CMV-p53 without adverse effects at doses of 1 x 108 pfu. The response to Ad-CMV-p53 showed significant survival duration in each dose regimen, with a survival time greater than that of untreated animals (P = 0.0173). However, no statistically significant survival advantage was observed between Ad-CMV-p53- and Ad-CMV-βgal-treated mice. Conclusions. These studies show that at the adenovirus dose and administration regimen used, there is effective but not specific 2774 tumor growth inhibition in vivo. Efficient introduction of biologically active genes into tumor cells would greatly facilitate cancer therapy. Thus, although promising, these results caution that much effort will be required to realize the potential for clinical application of adenovirus-based ovarian cancer gene therapy.

Original languageEnglish (US)
Pages (from-to)197-204
Number of pages8
JournalGynecologic oncology
Issue number3
StatePublished - Jun 1998

ASJC Scopus subject areas

  • Oncology
  • Obstetrics and Gynecology


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