A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1

In the world of today, virotherapy is one of the rapidly developing areas in the treatment of cancer, and its advantage is selective destruction of cancer cells with minimizing the destructive effect on normal cells of the body. A promising basis for the creation of oncolytic drugs is orthopoxviruse...

Full description

Saved in:
Bibliographic Details
Main Authors: R. A. Maksyutov, I. V. Kolosova, T. V. Tregubchak, I. A. Razumov, S. N. Shchelkunov
Format: Article
Language:English
Published: Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 2017-02-01
Series:Вавиловский журнал генетики и селекции
Subjects:
Online Access:https://vavilov.elpub.ru/jour/article/view/876
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832575247129247744
author R. A. Maksyutov
I. V. Kolosova
T. V. Tregubchak
I. A. Razumov
S. N. Shchelkunov
author_facet R. A. Maksyutov
I. V. Kolosova
T. V. Tregubchak
I. A. Razumov
S. N. Shchelkunov
author_sort R. A. Maksyutov
collection DOAJ
description In the world of today, virotherapy is one of the rapidly developing areas in the treatment of cancer, and its advantage is selective destruction of cancer cells with minimizing the destructive effect on normal cells of the body. A promising basis for the creation of oncolytic drugs is orthopoxviruses, which have a number of advantages over other viral vectors, and one of these advantages is a large capacity of the genome, which allows genes encoding proteins with antitumor properties to be cloned into their genome. In this study, we compared the replicative properties of ten variants of vaccinia virus (the strain LIVP of VACV) using human glioblastoma cell culture; some of these viruses have additional genes, such as the gene encoding granulocyte-macrophage colony stimulating factor, gene encoding apoptosis-inducing protein TRAIL and gene encoding green fluorescent protein. Furthermore, the virus with five virulence genes deleted (genes encoding hemagglutinin, γ-interferonbinding protein, thymidine kinase, complementbinding protein and Bcl2-like inhibitor of apoptosis), which has significantly lower reactogenicity and neurovirulence compared to the original strain LIVP of VACV, was studied. These data suggest that variants of vaccinia virus with a defective gene encoding thymidine kinase most actively replicate in glioblastoma cell culture.
format Article
id doaj-art-a5b565612aef4eb69a654eea688ab9fe
institution Kabale University
issn 2500-3259
language English
publishDate 2017-02-01
publisher Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders
record_format Article
series Вавиловский журнал генетики и селекции
spelling doaj-art-a5b565612aef4eb69a654eea688ab9fe2025-02-01T09:58:04ZengSiberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and BreedersВавиловский журнал генетики и селекции2500-32592017-02-0120694995310.18699/VJ16.207563A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1R. A. Maksyutov0I. V. Kolosova1T. V. Tregubchak2I. A. Razumov3S. N. Shchelkunov4State Research Center of Virology and Biotechnology ”Vector”,State Research Center of Virology and Biotechnology ”Vector”State Research Center of Virology and Biotechnology ”Vector”Institute of Cytology and Genetics SB RASState Research Center of Virology and Biotechnology ”Vector” Institute of Cytology and Genetics SB RASIn the world of today, virotherapy is one of the rapidly developing areas in the treatment of cancer, and its advantage is selective destruction of cancer cells with minimizing the destructive effect on normal cells of the body. A promising basis for the creation of oncolytic drugs is orthopoxviruses, which have a number of advantages over other viral vectors, and one of these advantages is a large capacity of the genome, which allows genes encoding proteins with antitumor properties to be cloned into their genome. In this study, we compared the replicative properties of ten variants of vaccinia virus (the strain LIVP of VACV) using human glioblastoma cell culture; some of these viruses have additional genes, such as the gene encoding granulocyte-macrophage colony stimulating factor, gene encoding apoptosis-inducing protein TRAIL and gene encoding green fluorescent protein. Furthermore, the virus with five virulence genes deleted (genes encoding hemagglutinin, γ-interferonbinding protein, thymidine kinase, complementbinding protein and Bcl2-like inhibitor of apoptosis), which has significantly lower reactogenicity and neurovirulence compared to the original strain LIVP of VACV, was studied. These data suggest that variants of vaccinia virus with a defective gene encoding thymidine kinase most actively replicate in glioblastoma cell culture.https://vavilov.elpub.ru/jour/article/view/876glioblastoma cell culturevirotherapyoncolytic virus
spellingShingle R. A. Maksyutov
I. V. Kolosova
T. V. Tregubchak
I. A. Razumov
S. N. Shchelkunov
A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
Вавиловский журнал генетики и селекции
glioblastoma cell culture
virotherapy
oncolytic virus
title A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
title_full A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
title_fullStr A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
title_full_unstemmed A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
title_short A comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture U87 and monkey kidney cell culture CV-1
title_sort comparative study of replicative properties of antitumor recombinant vaccinia viruses on human glioblastoma cell culture u87 and monkey kidney cell culture cv 1
topic glioblastoma cell culture
virotherapy
oncolytic virus
url https://vavilov.elpub.ru/jour/article/view/876
work_keys_str_mv AT ramaksyutov acomparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT ivkolosova acomparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT tvtregubchak acomparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT iarazumov acomparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT snshchelkunov acomparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT ramaksyutov comparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT ivkolosova comparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT tvtregubchak comparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT iarazumov comparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1
AT snshchelkunov comparativestudyofreplicativepropertiesofantitumorrecombinantvacciniavirusesonhumanglioblastomacellcultureu87andmonkeykidneycellculturecv1