Cargando…

Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells

Treatment trends of retinoblastoma (RB) have gradually evolved from eye enucleation and external radiation to local treatment. Combined treatment with an oncolytic virus and chemotherapy is currently a new method in RB treatment. To investigate the therapeutic effect of oncolytic adenovirus SG600 in...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Xin, Wang, Haibo, Jia, Renbing, Cun, Biyun, Zhao, Xiaoping, Zhou, Yixiong, Xu, Xiaofang, Qian, Guanxiang, Ge, Shengfang, Fan, Xianqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472711/
https://www.ncbi.nlm.nih.gov/pubmed/23109819
http://dx.doi.org/10.3390/ijms130910736
_version_ 1782246640069902336
author Song, Xin
Wang, Haibo
Jia, Renbing
Cun, Biyun
Zhao, Xiaoping
Zhou, Yixiong
Xu, Xiaofang
Qian, Guanxiang
Ge, Shengfang
Fan, Xianqun
author_facet Song, Xin
Wang, Haibo
Jia, Renbing
Cun, Biyun
Zhao, Xiaoping
Zhou, Yixiong
Xu, Xiaofang
Qian, Guanxiang
Ge, Shengfang
Fan, Xianqun
author_sort Song, Xin
collection PubMed
description Treatment trends of retinoblastoma (RB) have gradually evolved from eye enucleation and external radiation to local treatment. Combined treatment with an oncolytic virus and chemotherapy is currently a new method in RB treatment. To investigate the therapeutic effect of oncolytic adenovirus SG600 in combination with vincristine (VCR) on retinoblastoma in vitro, the cell viability, cell cycle effects and apoptotic activity of HXO-RB(44) cells treated with SG600, VCR or SG600 plus VCR were measured using a cell counting kit-8-based procedure and flow cytometry. Western blot analysis for Akt, p-Akt, p-p53 and p-Rb protein was performed to investigate the underlying mechanisms of combined therapy. The combination therapy exerted a synergistic antitumor effect via a type of G(2)/M and S phase arrest rather than the induction of apoptosis. The combination of VCR and SG600 further reduced Akt phosphorylation compared with cells treated with VCR alone, suggesting that SG600 could overcome chemoresistance, perhaps by down-regulating Akt in RB cells. An increase in the expression of p-p53 and decrease in p-Rb expression in HXO-RB(44) after co-treatment might be associated with cell cycle block. Western blot examination revealed that VCR might enhance SG600 replication. These results suggest that viro-chemo combination therapy is a feasible and potentially promising approach for the treatment of retinoblastoma.
format Online
Article
Text
id pubmed-3472711
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Molecular Diversity Preservation International (MDPI)
record_format MEDLINE/PubMed
spelling pubmed-34727112012-10-29 Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells Song, Xin Wang, Haibo Jia, Renbing Cun, Biyun Zhao, Xiaoping Zhou, Yixiong Xu, Xiaofang Qian, Guanxiang Ge, Shengfang Fan, Xianqun Int J Mol Sci Article Treatment trends of retinoblastoma (RB) have gradually evolved from eye enucleation and external radiation to local treatment. Combined treatment with an oncolytic virus and chemotherapy is currently a new method in RB treatment. To investigate the therapeutic effect of oncolytic adenovirus SG600 in combination with vincristine (VCR) on retinoblastoma in vitro, the cell viability, cell cycle effects and apoptotic activity of HXO-RB(44) cells treated with SG600, VCR or SG600 plus VCR were measured using a cell counting kit-8-based procedure and flow cytometry. Western blot analysis for Akt, p-Akt, p-p53 and p-Rb protein was performed to investigate the underlying mechanisms of combined therapy. The combination therapy exerted a synergistic antitumor effect via a type of G(2)/M and S phase arrest rather than the induction of apoptosis. The combination of VCR and SG600 further reduced Akt phosphorylation compared with cells treated with VCR alone, suggesting that SG600 could overcome chemoresistance, perhaps by down-regulating Akt in RB cells. An increase in the expression of p-p53 and decrease in p-Rb expression in HXO-RB(44) after co-treatment might be associated with cell cycle block. Western blot examination revealed that VCR might enhance SG600 replication. These results suggest that viro-chemo combination therapy is a feasible and potentially promising approach for the treatment of retinoblastoma. Molecular Diversity Preservation International (MDPI) 2012-08-27 /pmc/articles/PMC3472711/ /pubmed/23109819 http://dx.doi.org/10.3390/ijms130910736 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Song, Xin
Wang, Haibo
Jia, Renbing
Cun, Biyun
Zhao, Xiaoping
Zhou, Yixiong
Xu, Xiaofang
Qian, Guanxiang
Ge, Shengfang
Fan, Xianqun
Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title_full Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title_fullStr Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title_full_unstemmed Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title_short Combined Treatment with an Oncolytic Adenovirus and Antitumor Activity of Vincristine against Retinoblastoma Cells
title_sort combined treatment with an oncolytic adenovirus and antitumor activity of vincristine against retinoblastoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472711/
https://www.ncbi.nlm.nih.gov/pubmed/23109819
http://dx.doi.org/10.3390/ijms130910736
work_keys_str_mv AT songxin combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT wanghaibo combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT jiarenbing combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT cunbiyun combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT zhaoxiaoping combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT zhouyixiong combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT xuxiaofang combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT qianguanxiang combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT geshengfang combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells
AT fanxianqun combinedtreatmentwithanoncolyticadenovirusandantitumoractivityofvincristineagainstretinoblastomacells