Original Article
Cancer Gene Therapy (2004) 11, 555–569. doi:10.1038/sj.cgt.7700735 Published online 2 July 2004
Antitumor efficacy and tumor-selective replication with a single intravenous injection of OAS403, an oncolytic adenovirus dependent on two prevalent alterations in human cancer
Patricia C Ryan1, John L Jakubczak1, David A Stewart1, Lynda K Hawkins1,a, Cheng Cheng1, Lori M Clarke1, Shanthi Ganesh1,a, Carl Hay1, Ying Huang1, Michele Kaloss1, Anthony Marinov1, Sandrina S Phipps1, P Seshidhar Reddy1,a, Pamela S Shirley1, Yelena Skripchenko1, Ling Xu1, Jingping Yang1, Suzanne Forry-Schaudies1 and Paul L Hallenbeck1,b
1Genetic Therapy, Inc. (a Novartis Company), Gaithersburg, Maryland 20878, USA
Correspondence: Dr Paul L Hallenbeck, PhD, 7461 Rosewood Manor Lane, Gaithersburg, MD 20882, USA. E-mail: phallenbeck@comcast.net
aCurrent address: Cell Genesys, Inc., 500 Forbes Blvd., South San Francisco, CA 94080, USA.
bCurrent address: NeotropiX, Inc. 7461 Rosewood Manor Lane, Gaithersburg, MD 20882, USA.
Received 27 January 2004; Published online 2 July 2004.
Abstract
A potentially promising treatment of metastatic cancer is the systemic delivery of oncolytic adenoviruses. This requires engineering viruses which selectively replicate in tumors. We have constructed such an oncolytic adenovirus, OAS403, in which two early region genes are under the control of tumor-selective promoters that play a role in two key pathways involved in tumorigenesis. The early region E1A is controlled by the promoter for the E2F-1 gene, a transcription factor that primarily upregulates genes for cell growth. The E4 region is under control of the promoter for human telomerase reverse transcriptase, a gene upregulated in most cancer cells. OAS403 was evaluated in vitro on a panel of human cells and found to elicit tumor-selective cell killing. Also, OAS403 was less toxic in human hepatocyte cultures, as well as in vivo when compared to an oncolytic virus that lacked selective E4 control. A single intravenous injection of 3
1012 vp/kg in a Hep3B xenograft mouse tumor model led to significant antitumor efficacy. Additionally, systemic administration in a pre-established LNCaP prostate tumor model resulted in over 80% complete tumor regressions at a tolerable dose. Vector genome copy number was measured in tumors and livers at various times following tail vein injection and showed a selective time-dependent increase in tumors but not livers over 29 days. Furthermore, efficacy was significantly improved when OAS403 treatment was combined with doxorubicin. This virus holds promise for the treatment of a broad range of human cancers including metastatic disease.
Keywords:
oncolytic viruses, Adenoviridae, cell cycle, transcription factor E2F-1, Telomerase, neoplasms
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