Abstract
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is an aggressive and largely incurable hematologic malignancy originating from plasmacytoid dendritic cells (pDCs). Using RNAi screening, we identified the E-box transcription factor TCF4 as a master regulator of the BPDCN oncogenic program. TCF4 served as a faithful diagnostic marker of BPDCN, and its downregulation caused the loss of the BPDCN-specific gene expression program and apoptosis. High-throughput drug screening revealed that bromodomain and extra-terminal domain inhibitors (BETis) induced BPDCN apoptosis, which was attributable to disruption of a BPDCN-specific transcriptional network controlled by TCF4-dependent super-enhancers. BETis retarded the growth of BPDCN xenografts, supporting their clinical evaluation in this recalcitrant malignancy.
Keywords:
BPDCN; BRD4; HTS; TCF4; super-enhancer.
Published by Elsevier Inc.
MeSH terms
-
Animals
-
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / antagonists & inhibitors
-
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics*
-
Cell Cycle Proteins
-
Cell Line, Tumor
-
Dendritic Cells / metabolism
-
Dendritic Cells / pathology*
-
Gene Expression Regulation, Neoplastic
-
Gene Regulatory Networks
-
HL-60 Cells
-
Hematologic Neoplasms / drug therapy*
-
Hematologic Neoplasms / genetics
-
Hematologic Neoplasms / pathology
-
Humans
-
Jurkat Cells
-
Mice
-
Nuclear Proteins / genetics*
-
RNA, Small Interfering / administration & dosage*
-
RNA, Small Interfering / pharmacology
-
Small Molecule Libraries / administration & dosage*
-
Small Molecule Libraries / pharmacology
-
Transcription Factor 4
-
Transcription Factors / antagonists & inhibitors
-
Transcription Factors / genetics*
-
Xenograft Model Antitumor Assays
Substances
-
BRD4 protein, human
-
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
-
Cell Cycle Proteins
-
Nuclear Proteins
-
RNA, Small Interfering
-
Small Molecule Libraries
-
TCF4 protein, human
-
Transcription Factor 4
-
Transcription Factors