Cancer Cell
Volume 26, Issue 6, 8 December 2014, Pages 909-922
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Article
Targeting Transcriptional Addictions in Small Cell Lung Cancer with a Covalent CDK7 Inhibitor

https://doi.org/10.1016/j.ccell.2014.10.019Get rights and content
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Highlights

  • SCLC is vulnerable to inhibition of RNAPII-mediated transcription by THZ1

  • SCLC super-enhancers associate with proto-oncogenes and key SCLC identity genes

  • THZ1 preferentially targets super-enhancer-driven transcription factor genes

  • THZ1 represents a first-in-class experimental agent for the treatment of SCLC

Summary

Small cell lung cancer (SCLC) is an aggressive disease with high mortality, and the identification of effective pharmacological strategies to target SCLC biology represents an urgent need. Using a high-throughput cellular screen of a diverse chemical library, we observe that SCLC is sensitive to transcription-targeting drugs, in particular to THZ1, a recently identified covalent inhibitor of cyclin-dependent kinase 7. We find that expression of super-enhancer-associated transcription factor genes, including MYC family proto-oncogenes and neuroendocrine lineage-specific factors, is highly vulnerability to THZ1 treatment. We propose that downregulation of these transcription factors contributes, in part, to SCLC sensitivity to transcriptional inhibitors and that THZ1 represents a prototype drug for tailored SCLC therapy.

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