Targeted Cancer Gene Therapy Using a Hypoxia Inducible Factor–Dependent Oncolytic Adenovirus Armed with Interleukin-4

• Type of Material: Article
• Authors: Dawn E. Post, Emory University; Eric M. Sandberg, Emory University; Michele M. Kyle, State University of New York Upstate Medical University; Narra Sarojini Devi, Emory University; Daniel J Brat, Emory University; Zhiheng Xu, Emory University; Mourad Tighiouart, Emory University; Erwin Van Meir, Emory University
• Language: English
• Date: 2007-07-15
• Publisher: American Association for Cancer Research
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2007, American Association for Cancer Research
• Final Published Version (URL): http://cancerres.aacrjournals.org/content/67/14/6872
• Title of Journal or Parent Work: Cancer Research
• ISSN: 0008-5472
• Volume: 67
• Issue: 14
• Start Page: 6872
• End Page: 6881
• Grant/Funding Information: Grant support: NIH grants NS49300 (D.E. Post) and CA87830, CA86335, and NS41403 (E.G. Van Meir).

Abstract

There is a need for novel therapies targeting hypoxic cells in tumors. These cells are associated with tumor resistance to therapy and express hypoxia inducible factor-1 (HIF-1), a transcription factor that mediates metabolic adaptation to hypoxia and activates tumor angiogenesis. We previously developed an oncolytic adenovirus (HYPR-Ad) for the specific killing of hypoxic/HIF-active tumor cells, which we now armed with an interleukin-4 gene (HYPR-Ad-IL4). We designed HYPR-Ad-IL4 by cloning the Ad E1A viral replication and IL-4 genes under the regulation of a bidirectional hypoxia/HIF-responsive promoter. The IL-4 cytokine was chosen for its ability to induce a strong host antitumor immune response and its potential antiangiogenic activity. HYPR-Ad-IL4 induced hypoxia-dependent IL-4 expression, viral replication, and conditional cytolysis of hypoxic, but not normoxic cells. The treatment of established human tumor xenografts with HYPR-Ad-IL4 resulted in rapid and maintained tumor regression with the same potency as that of wild-type dl309-Ad. HYPR-Ad-IL4–treated tumors displayed extensive necrosis, fibrosis, and widespread viral replication. Additionally, these tumors contained a distinctive leukocyte infiltrate and prominent hypoxia. The use of an oncolytic Ad that locally delivers IL-4 to tumors is novel, and we expect that HYPR-Ad-IL4 will have broad therapeutic use for all solid tumors that have hypoxia or active HIF, regardless of tissue origin or genetic alterations.