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Tumor suppression by apoptotic and anti‐angiogenic effects of mortalin‐targeting adeno‐oncolytic virus
Author(s) -
Yoo Ji Young,
Ryu Jihoon,
Gao Ran,
Yaguchi Tomoko,
Kaul Sunil C.,
Wadhwa Renu,
Yun ChaeOk
Publication year - 2010
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1471
Subject(s) - oncolytic virus , cancer research , biology , apoptosis , gene silencing , in vivo , cancer cell , suicide gene , virus , genetic enhancement , carcinogenesis , adeno associated virus , oncolytic adenovirus , cancer , immunology , gene , vector (molecular biology) , biochemistry , genetics , microbiology and biotechnology , recombinant dna
Background Adeno‐oncolytic (Adon) viruses offer an effective cancer therapeutic tool with several advantages, including wide host cell permeability, high transduction efficiency, safety, tumor selectivity, non‐invasiveness, high genetic modifiability and high level of expression of the integrated transgenes. Armed Adon viruses in which the therapeutic efficacy of virus is enhanced by their coupling with cytotoxic, anti‐angiogenic or anti‐vascular gene products have gained importance because they engage additional mechanisms for tumor cell killing. In the present study, we selected mortalin, a stress chaperone that is tightly involved in human carcinogenesis, constructed a mortalin‐targeting Adon (mot‐Adon) virus and examined its therapeutic potential both in vitro and in vivo.Methods Mortalin‐targeting plasmid and viral vectors that harbored mortalin‐specific small interfering RNA sequences were constructed. The therapeutic value of these vectors was investigated in vitro and in vivo by cell culture and nude mice tumor models. Results We demonstrate that the mot‐Adon virus has selective cytotoxicity for human cancer cells in vitro. Retrovirus‐mediated overexpression of mortalin protected the cells against mot‐Adon virus, confirming that mortalin silencing was the real cause of cancer cell death. Although mortalin overexpression enhanced malignant properties of cancer cells in breast xenograft models, mot‐Adon virus elicited an enhanced anti‐tumor effect. Immunohistochemical examination of the tumors showed that the mot‐Adon virus caused enhanced apoptosis (mediated by reactivation of p53) and suppression of microvessel formation. Conclusions Mortalin is up‐regulated in a large variety of tumors and hence mot‐Adon virus is proposed as a candidate cancer therapeutic agent. Copyright © 2010 John Wiley & Sons, Ltd.