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Loss of synergistic transcriptional feedback loops drives diverse B-cell cancers.
- Source :
-
EBioMedicine [EBioMedicine] 2021 Sep; Vol. 71, pp. 103559. Date of Electronic Publication: 2021 Aug 27. - Publication Year :
- 2021
-
Abstract
- Background: The most common B-cell cancers, chronic lymphocytic leukemia/lymphoma (CLL), follicular and diffuse large B-cell (FL, DLBCL) lymphomas, have distinct clinical courses, yet overlapping "cell-of-origin". Dynamic changes to the epigenome are essential regulators of B-cell differentiation. Therefore, we reasoned that these distinct cancers may be driven by shared mechanisms of disruption in transcriptional circuitry.<br />Methods: We compared purified malignant B-cells from 52 patients with normal B-cell subsets (germinal center centrocytes and centroblasts, naïve and memory B-cells) from 36 donor tonsils using >325 high-resolution molecular profiling assays for histone modifications, open chromatin (ChIP-, FAIRE-seq), transcriptome (RNA-seq), transcription factor (TF) binding, and genome copy number (microarrays).<br />Findings: From the resulting data, we identified gains in active chromatin in enhancers/super-enhancers that likely promote unchecked B-cell receptor signaling, including one we validated near the immunoglobulin superfamily receptors FCMR and PIGR. More striking and pervasive was the profound loss of key B-cell identity TFs, tumor suppressors and their super-enhancers, including EBF1, OCT2(POU2F2), and RUNX3. Using a novel approach to identify transcriptional feedback, we showed that these core transcriptional circuitries are self-regulating. Their selective gain and loss form a complex, iterative, and interactive process that likely curbs B-cell maturation and spurs proliferation.<br />Interpretation: Our study is the first to map the transcriptional circuitry of the most common blood cancers. We demonstrate that a critical subset of B-cell TFs and their cognate enhancers form self-regulatory transcriptional feedback loops whose disruption is a shared mechanism underlying these diverse subtypes of B-cell lymphoma.<br />Funding: National Institute of Health, Siteman Cancer Center, Barnes-Jewish Hospital Foundation, Doris Duke Foundation.<br />Competing Interests: Declaration of Competing Interest The authors declare no potential conflicts of interest.<br /> (Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Aged
Aged, 80 and over
B-Lymphocytes immunology
Biomarkers
Cell Transformation, Neoplastic metabolism
Chromatin Immunoprecipitation Sequencing
Computational Biology methods
DNA Copy Number Variations
Enhancer Elements, Genetic
Epigenesis, Genetic
Female
Gene Expression Profiling
Humans
Immunophenotyping
Leukemia, B-Cell diagnosis
Leukemia, B-Cell metabolism
Lymphoma, B-Cell diagnosis
Lymphoma, B-Cell metabolism
Male
Middle Aged
Models, Biological
Oncogenes
Signal Transduction
Transcription Factors metabolism
B-Lymphocytes metabolism
Cell Transformation, Neoplastic genetics
Gene Expression Regulation, Neoplastic
Leukemia, B-Cell etiology
Lymphoma, B-Cell etiology
Transcription, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 2352-3964
- Volume :
- 71
- Database :
- MEDLINE
- Journal :
- EBioMedicine
- Publication Type :
- Academic Journal
- Accession number :
- 34461601
- Full Text :
- https://doi.org/10.1016/j.ebiom.2021.103559