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Related Experiment Video

Updated: Jan 27, 2026

Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
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Tracing MYC Expression for Small Molecule Discovery.

Jutta Steinberger1, Francis Robert1, Maxime Hallé1

  • 1Department of Biochemistry, McGill University, Montreal, QC H3G 1Y6, Canada.

Cell Chemical Biology
|March 19, 2019
PubMed
Summary
This summary is machine-generated.

Developing new therapeutic strategies is crucial for targeting MYC (pronounced “my-seek”). Researchers created a novel assay using CRISPR/Cas9 to monitor MYC expression, identifying potent inhibitors like cardiac glycosides.

Keywords:
CRISPR/Cas9MYC expressionchemical biologydrug discoverydrug repurposinggenome engineeringmultiple myelomasphenotype-based assaytarget identification

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Area of Science:

  • Oncology
  • Molecular Biology
  • Drug Discovery

Background:

  • Targeting MYC, a key oncogene, remains challenging for cancer therapeutics.
  • Existing methods for monitoring MYC expression are insufficient for drug screening.

Purpose of the Study:

  • To develop a novel phenotype-based assay for monitoring MYC expression in multiple myeloma cells.
  • To identify novel MYC expression modulators using a high-throughput screening approach.

Main Methods:

  • Engineered co-expression of MYC and an unstable variant of GFP using CRISPR/Cas9 at the endogenous MYC locus.
  • Implemented a fluorescence readout as a surrogate for MYC expression.
  • Conducted a pilot screen of approximately 10,000 compounds.

Main Results:

  • Successfully established a CRISPR/Cas9-engineered MYC expression assay.
  • Identified cardiac glycosides and cytoskeletal disruptors as potent inhibitors of MYC expression.
  • Demonstrated the utility of this assay for identifying gene expression modulators.

Conclusions:

  • CRISPR/Cas9 engineering provides a powerful platform for developing phenotype-based drug discovery assays.
  • The developed assay enables efficient screening for MYC expression modulators.
  • Novel classes of compounds, including cardiac glycosides, show potential for targeting MYC-driven cancers.