| Literature DB >> 30880156 |
Jutta Steinberger1, Francis Robert1, Maxime Hallé1, David E Williams2, Regina Cencic1, Neha Sawhney3, Dylan Pelletier1, Philip Williams4, Yasuhiro Igarashi5, John A Porco6, Abimael D Rodriguez7, Brigitte Kopp8, Brian Bachmann3, Raymond J Andersen2, Jerry Pelletier9.
Abstract
Our inability to effectively "drug" targets such as MYC for therapeutic purposes requires the development of new approaches. We report on the implementation of a phenotype-based assay for monitoring MYC expression in multiple myeloma cells. The open reading frame (ORF) encoding an unstable variant of GFP was engineered immediately downstream of the MYC ORF using CRISPR/Cas9, resulting in co-expression of both proteins from the endogenous MYC locus. Using fluorescence readout as a surrogate for MYC expression, we implemented a pilot screen in which ∼10,000 compounds were prosecuted. Among known MYC expression inhibitors, we identified cardiac glycosides and cytoskeletal disruptors to be quite potent. We demonstrate the power of CRISPR/Cas9 engineering in establishing phenotype-based assays to identify gene expression modulators.Entities:
Keywords: CRISPR/Cas9; MYC expression; chemical biology; drug discovery; drug repurposing; genome engineering; multiple myelomas; phenotype-based assay; target identification
Mesh:
Substances:
Year: 2019 PMID: 30880156 PMCID: PMC6525070 DOI: 10.1016/j.chembiol.2019.02.007
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116