Regression of Human Prostate Tumors and Metastases in Nude Mice following Treatment with the Recombinant Oncolytic Vaccinia Virus GLV-1h68

Virotherapy using oncolytic vaccinia virus strains is one of the most promising new strategies for cancer therapy. In the current study, we analyzed the therapeutic efficacy of the oncolytic vaccinia virus GLV-1h68 against two human prostate cancer cell lines DU-145 and PC-3 in cell culture and in t...

Full description

Saved in:
Bibliographic Details
Published inBioMed research international Vol. 2010; no. 2010; pp. 1 - 11
Main Authors Gentschev, Ivaylo, Donat, Ulrike, Hofmann, Elisabeth, Weibel, Stephanie, Adelfinger, Marion, Raab, Viktoria, Heisig, Martin, Chen, Nanhai G., Yu, Yong A., Stritzker, Jochen, Szalay, Aladar A.
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Puplishing Corporation 01.01.2010
Hindawi Publishing Corporation
Dar al -Nasr -al-Llktruni
Hindawi Limited
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Virotherapy using oncolytic vaccinia virus strains is one of the most promising new strategies for cancer therapy. In the current study, we analyzed the therapeutic efficacy of the oncolytic vaccinia virus GLV-1h68 against two human prostate cancer cell lines DU-145 and PC-3 in cell culture and in tumor xenograft models. By viral proliferation assays and cell survival tests, we demonstrated that GLV-1h68 was able to infect, replicate in, and lyse these prostate cancer cells in culture. In DU-145 and PC-3 tumor xenograft models, a single intravenous injection with GLV-1h68 resulted in a significant reduction of primary tumor size. In addition, the GLV-1h68-infection led to strong inflammatory and oncolytic effects resulting in drastic reduction of regional lymph nodes with PC-3 metastases. Our data documented that the GLV-1h68 virus has a great potential for treatment of human prostate carcinoma.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Academic Editor: Colin Cooper
ISSN:1110-7243
2314-6133
1110-7251
2314-6141
DOI:10.1155/2010/489759