Korean J Urol.  2004 Nov;45(11):1156-1161.

The Effect of Recombinant Baculovirus (BacG-CMV-P53) Mediated Gene Therapy in the HT-1376 Bladder Cancer Cell Line

Affiliations
  • 1Departments of Urology, The Catholic University of Korea. uroljy@catholic.ac.kr
  • 2Departments of Microbiology, The Catholic University of Korea.

Abstract

PURPOSE: In preliminary studies, it was found that mammalian cells can be infected by recombinant baculovirus in vitro. Therefore, the potential use of recombinant baculovirus(BacG-cytonegalovirus(CMV)-P53) for the bladder gene therapy was investigated.
MATERIALS AND METHODS
The recombinant Baculovirus(BV) pseudotyped was developed with the vesicular stomatitis virus(VSV) G protein. The presence of the VSV-G protein in purified BV preparations was confirmed by Western blotting analysis. The bladder cancer cells of human(HT-1376) were infected with various multiplicity of infection(MOI) of the BV, and the percentage of apoptotic cells determined by methyl thiazolyl tetrazolium(MTT) assay.
RESULTS
The suppression effect of the recombinant BV with a P53 insertion in human bladder cancer cells(HT-1376) increased as the MOI of the recombinant BV increased; 100% cell survival in the group with PBS, and 81.6+/-4.3, 52.0+/-5.6 and 39.8+/-3.7% at 1, 10 and 100 MOI, respectively (p<0.05).
CONCLUSIONS
Significant growth suppression was observed following infection with BacG-CMV-P53 in a human bladder cancer cell line. This observation suggests that BacG-CMV-P53 may be a potentially effective agent to prevent recurrence for P53 mutated bladder cancer. Bladder gene therapy using recombinant baculovirus could be a safe and effective treatment of bladder cancer.

Keyword

Baculovirus; Bladder cancer; Gene therapy

MeSH Terms

Baculoviridae*
Blotting, Western
Cell Line*
Cell Survival
Genetic Therapy*
GTP-Binding Proteins
Humans
Recurrence
Urinary Bladder Neoplasms*
Urinary Bladder*
Vesicular Stomatitis
GTP-Binding Proteins
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