Literature DB >> 16467873

Targeting gene-virotherapy of cancer.

Xin Yuan Liu1, Jin Fa Gu.   

Abstract

Our purpose is to completely elimination of xenograft tumor in animal tumor model in order to work out a protocal for the cure of patient. Gene therapy and viral therapy for cancer have got some therapeutic effects, but both have no great breakthrough. Therefore, we worked out a new strategy called Targeting Gene-Virotherapy of Cancer which is a combination of the advantage of gene therapy and virotherapy. This new strategy has stronger antitumor effect than either of them alone. A tumor specific replicative adenovirus vector ZD55 (E1B 55KD deleted Adv.) which is similar to ONYX-015 in targeting fuction but significant different in construction was produced and various single therapeutic gene was inserted into ZD55. Now such a conception as Targeting Gene-Virotherapy of Cancer was raised and systemically studied before, although there are some works on ONYX-015-tk, -cd or cd/-tk etc. separately. The antitumor effect of ZD55-Gene (for example IL-24 gene) is much better than ZD55 (virotherapy) alone and hundred fold high than that of Ad-IL-24 (gene therapy) alone. ZD55-IL-24 was in preclinal studying in the ZD55-IL-24 therapy, completely elimination of tumor mass was occurred in some mice but not in all mice, that means one gene was not effictive enough to eliminate all the tumor mass in all mice. Therefore two genes with compensative or synergetic effect were inserted into ZD55 separately and used in combination. This strategy was called Targeting Dual Gene-Virotherapy of Cancer (with PCT patent). Then much better results were obtained and all the xenograft tumor masses were completely eliminated in all mice, if two suitable genes were chosen. On the basis of the initiation of two gene results, it was thought about that using two tumors promoter to control the virus vector will be better for the targeting effect and the safty of the drugs. Then double tumor controlled virus vector harboring two genes for cancer therapy was worked out. Better results have been obtained and another patent has been applied. This antitumor strategy could be used to kill all the tumor cells completely in all mice with minimum damage to normal cells.

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Year:  2006        PMID: 16467873     DOI: 10.1038/sj.cr.7310005

Source DB:  PubMed          Journal:  Cell Res        ISSN: 1001-0602            Impact factor:   25.617


  14 in total

1.  Oncolytic adenovirus SG600-IL24 selectively kills hepatocellular carcinoma cell lines.

Authors:  Xin-Bo Xue; Chao-Wen Xiao; Hui Zhang; Ai-Guo Lu; Wei Gao; Zhu-Qing Zhou; Xin-Lai Guo; Ming-An Zhong; Yao Yang; Cong-Jun Wang
Journal:  World J Gastroenterol       Date:  2010-10-07       Impact factor: 5.742

2.  Targeted genetic modification of cell lines for recombinant protein production.

Authors:  Niall Barron; Olga Piskareva; Mohan Muniyappa
Journal:  Cytotechnology       Date:  2007-02-28       Impact factor: 2.058

Review 3.  Targeting adeno-associated virus and adenoviral gene therapy for hepatocellular carcinoma.

Authors:  Yi-Gang Wang; Pan-Pan Huang; Rong Zhang; Bu-Yun Ma; Xiu-Mei Zhou; Yan-Fang Sun
Journal:  World J Gastroenterol       Date:  2016-01-07       Impact factor: 5.742

4.  Dichloroacetate (DCA) enhances tumor cell death in combination with oncolytic adenovirus armed with MDA-7/IL-24.

Authors:  Lianli Xiao; Xin Li; Na Niu; Jing Qian; Guoliang Xie; Yigang Wang
Journal:  Mol Cell Biochem       Date:  2010-02-18       Impact factor: 3.396

5.  Enhancement of tumor cell death by combining cisplatin with an oncolytic adenovirus carrying MDA-7/IL-24.

Authors:  Yu-mei Wu; Kang-jian Zhang; Xue-tian Yue; Yi-qiang Wang; Yi Yang; Gong-chu Li; Na Li; Yi-gang Wang
Journal:  Acta Pharmacol Sin       Date:  2009-03-09       Impact factor: 6.150

6.  Synergistic suppression effect on tumor growth of hepatocellular carcinoma by combining oncolytic adenovirus carrying XAF1 with cisplatin.

Authors:  Buyun Ma; Yanchun Wang; Xiumei Zhou; Panpan Huang; Rong Zhang; Tao Liu; Caixia Cui; Xinyuan Liu; Yigang Wang
Journal:  J Cancer Res Clin Oncol       Date:  2014-09-21       Impact factor: 4.553

7.  MDA-7/IL-24 induces Bcl-2 denitrosylation and ubiquitin-degradation involved in cancer cell apoptosis.

Authors:  Hui Tian; Jing Wang; BaoFu Zhang; JieHui Di; FeiFei Chen; HuiZhong Li; LianTao Li; DongSheng Pei; JunNian Zheng
Journal:  PLoS One       Date:  2012-05-21       Impact factor: 3.240

8.  Oncolytic adenovirus armed with IL-24 inhibits the growth of breast cancer in vitro and in vivo.

Authors:  Wei Zhu; Lai Wei; Hongwei Zhang; Junxue Chen; Xinyu Qin
Journal:  J Exp Clin Cancer Res       Date:  2012-05-28

9.  Overexpression of tumor suppressor TSLC1 by a survivin-regulated oncolytic adenovirus significantly inhibits hepatocellular carcinoma growth.

Authors:  Guoqing He; Wen Lei; Shibin Wang; Ruijuan Xiao; Keni Guo; Yulong Xia; Xiumei Zhou; Kangjian Zhang; Xinyuan Liu; Yigang Wang
Journal:  J Cancer Res Clin Oncol       Date:  2012-01-12       Impact factor: 4.322

10.  A novel Golgi protein (GOLPH2)-regulated oncolytic adenovirus exhibits potent antitumor efficacy in hepatocellular carcinoma.

Authors:  Yigang Wang; Tao Liu; Panpan Huang; Hongfang Zhao; Rong Zhang; Buyun Ma; Kan Chen; Fang Huang; Xiumei Zhou; Caixia Cui; Xinyuan Liu
Journal:  Oncotarget       Date:  2015-05-30
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