Discovery of a Chemical Probe to Study Implications of BPTF Bromodomain Inhibition in Cellular and in vivo Experiments

Author:

Martinelli Paola1,Schaaf Otmar1,Mantoulidis Andreas1,Martin Laetitia J.1,Fuchs Julian E.1,Bader Gerd1,Gollner Andreas1,Wolkerstorfer Bernhard1,Rogers Catherine23,Balıkçı Esra23,Lipp Jesse J.1,Mischerikow Nikolai1,Doebel Sandra1,Gerstberger Thomas1,Sommergruber Wolfgang1,Huber Kilian V. M.23,Böttcher Jark1ORCID

Affiliation:

1. Boehringer Ingelheim RCV GmbH & Co KG Doktor-Boehringer-Gasse 5–11 1120 Vienna Austria

2. Target Discovery Institute Nuffield Department of Medicine University of Oxford OX3 7FZ Oxford UK

3. Centre for Medicines Discovery Nuffield Department of Medicine University of Oxford OX3 7FZ Oxford UK

Abstract

AbstractThe bromodomain and PHD‐finger containing transcription factor (BPTF) is part of the nucleosome remodeling factor (NURF) complex and has been implicated in multiple cancer types. Here, we report the discovery of a potent and selective chemical probe targeting the bromodomain of BPTF with an attractive pharmacokinetic profile enabling cellular and in vivo experiments in mice. Microarray‐based transcriptomics in presence of the probe in two lung cancer cell lines revealed only minor effects on the transcriptome. Profiling against a panel of cancer cell lines revealed that the antiproliferative effect does not correlate with BPTF dependency score in depletion screens. Both observations and the multi‐domain architecture of BPTF suggest that depleting the protein by proteolysis targeting chimeras (PROTACs) could be a promising strategy to target cancer cell proliferation. We envision that the presented chemical probe and the related negative control will enable the research community to further explore scientific hypotheses with respect to BPTF bromodomain inhibition.

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

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