Heat shock and heat shock protein 70i enhance the oncolytic effect of replicative adenovirus

Yosef S. Haviv, Jerry L. Blackwell, Hui Li, Minghui Wang, Xiaosheng Lei, David T. Curiel

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

Replication-competent viruses are currently being evaluated for their cancer cell-killing properties. These vectors are designed to induce tumor regression after selective viral propagation within the tumor. However, replication-competent viruses have not resulted heretofore in complete tumor eradication in the clinical setting. Recently, heat shock has been reported to partially alleviate replication restriction on an avian adenovirus (Ad) in a human lung cancer cell line. Therefore, we hypothesized that heat shock and overexpression of heat shock protein (hsp) would support the oncolytic effect of a replication-competent human Ad. To this end, we tested the oncolytic and burst kinetics of a replication-competent Ad after exposure to heat shock or to inducible hsp 70 overexpression by a replication-deficient Ad (Adhsp 70i). Heat-shock resulted in augmentation of Ad burst and oncolysis while decreasing total intracellular Ad DNA. Overexpression of hsp 70i also enhanced Ad-mediated oncolysis but did not decrease intracellular Ad DNA levels. We conclude that heat shock and Adhsp 70i enhance the Ad cell-killing potential via distinct mechanisms. A potential therapeutic implication would be the use of local hyperthermia to augment oncolysis by increasing the burst of replication-competent Ad. The role of hsp in Ad-mediated oncolysis should be additionally explored.

Original languageEnglish
Pages (from-to)8361-8365
Number of pages5
JournalCancer research
Volume61
Issue number23
StatePublished - Dec 1 2001
Externally publishedYes

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    Haviv, Y. S., Blackwell, J. L., Li, H., Wang, M., Lei, X., & Curiel, D. T. (2001). Heat shock and heat shock protein 70i enhance the oncolytic effect of replicative adenovirus. Cancer research, 61(23), 8361-8365.