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Article type: Research Article
Authors: Groot, Arjan J. | Gort, Eelke H. | van der Wall, Elsken | van Diest, Paul J. | Vooijs, Marc;
Affiliations: Department of Pathology, University Medical Center Utrecht, 3508 GA, Utrecht, The Netherlands | Department of Internal Medicine, University Medical Center Utrecht, 3508 GA, Utrecht, The Netherlands
Note: [] Corresponding author. E-mail: [email protected].
Abstract: Hypoxia is a hallmark of solid cancers and triggers the transcription of genes responsible for cell survival. The transcription factor Hypoxia-Inducible Factor 1 (HIF-1) is a key regulator in this response and frequently activated in human cancer. HIF-1 activation is associated with tumor aggressiveness and poor clinical outcome and, therefore, may provide an attractive therapeutic target. Here we provide a novel approach for HIF-1 targeted therapy using single-domain llama antibodies directed against the HIF-1α oxygen dependent degradation domain which encompass the N-terminal transactivation domain. Conditional expression of HIF intrabodies in mammalian cells interfered with binding to pVHL and inhibited hypoxia induced activation of endogenous target genes. Inducible intrabody targeting is a highly specific strategy for temporal protein inactivation and may have applications for disease treatment.
Keywords: Cancer, HIF, hypoxia, intrabody, single-chain antibody fragment, VHH
DOI: 10.3233/CLO-2008-0442
Journal: Analytical Cellular Pathology, vol. 30, no. 5, pp. 397-409, 2008
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