CDK7-Dependent Transcriptional Addiction in Triple-Negative Breast Cancer
Author(s) -
Yubao Wang,
Tinghu Zhang,
Nicholas Kwiatkowski,
Brian J. Abraham,
Tong Ihn Lee,
Shaozhen Xie,
Haluk Yuzugullu,
Thanh Von,
Heyuan Li,
Ziao Lin,
Daniel G. Stover,
Elgene Lim,
Zhigang C. Wang,
J. Dirk Iglehart,
Richard A. Young,
Nathanael S. Gray,
Jean J. Zhao
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.08.063
Subject(s) - biology , triple negative breast cancer , breast cancer , cancer research , addiction , cancer , genetics , computational biology , neuroscience
Triple-negative breast cancer (TNBC) is a highly aggressive form of breast cancer that exhibits extremely high levels of genetic complexity and yet a relatively uniform transcriptional program. We postulate that TNBC might be highly dependent on uninterrupted transcription of a key set of genes within this gene expression program and might therefore be exceptionally sensitive to inhibitors of transcription. Utilizing kinase inhibitors and CRISPR/Cas9-mediated gene editing, we show here that triple-negative but not hormone receptor-positive breast cancer cells are exceptionally dependent on CDK7, a transcriptional cyclin-dependent kinase. TNBC cells are unique in their dependence on this transcriptional CDK and suffer apoptotic cell death upon CDK7 inhibition. An "Achilles cluster" of TNBC-specific genes is especially sensitive to CDK7 inhibition and frequently associated with super-enhancers. We conclude that CDK7 mediates transcriptional addiction to a vital cluster of genes in TNBC and CDK7 inhibition may be a useful therapy for this challenging cancer.
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