Development of a Cell-Based Reporter Assay for Screening of Inhibitors of Hypoxia-Inducible Factor 2-Induced Gene Expression

Author:

Woldemichael Girma M.1,Vasselli James R.2,Gardella Roberta S.3,Mckee Tawnya C.1,Linehan W. Marston2,McMahon James B.1

Affiliation:

1. National Cancer Institute, Molecular Targets Development Program, Center for Cancer Research, Frederick, Maryland

2. National Cancer Institute, Clinical Research Center, Urologic Oncology Branch, Bethesda, Maryland

3. SAIC-Frederick, Inc., Basic Research Program, NCI-Frederick, Frederick, Maryland

Abstract

Reporter cell lines have been developed for the identification of inhibitors of gene expression enhanced by hypoxia-inducible factor 2, which has been implicated as a transcription factor involved in the tumorigenesis of clear cell renal carcinoma. Stably transformed reporter clones of the human renal clear cell carcinoma cell line 786-O were generated by transfection or retroviral infection. Luciferase reporter expression in the vectors used was driven by either the natural human vascular endothelial growth factor (VEGF) promoter-enhancer or by the VEGF and the human endothelial nitric oxide synthase enhancers modulating minimal human cytomegalovirus promoter. Utility of the generated reporter cell lines was validated by introducing the von Hippel-Lindau protein complex and testing for reporter inducibility by hypoxia. The dynamic range in reporter activity under hypoxic stress was found to be at least 30- to 40-fold, with a signal-to-noise ratio of 60:1. Properties of the cell lines such as tolerance to up to 3% DMSO, signal stability with multiple in vitro passages, and utility in both 96- and 384-well plate formats indicated their suitability for use in a high-throughput screen. In addition, the potential use of these reporter lines in the evaluation of high-throughput screening hits in vivo in various mice models has been demonstrated.

Publisher

Elsevier BV

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