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The NLRP3 inflammasome functions as a driver of the myelodysplastic syndrome phenotype
Abstract
Key Points: Key biological features of MDSs are explained by NLRP3 inflammasome activation, which drives pyroptotic cell death and β-catenin activation. Alarmin signals and founder gene mutations license this redox-sensitive inflammasome platform.
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“Similarly, NLRP3 priming and activation are exaggerated in aged human monocytes 201 .”
From Clonal haematopoiesis and dysregulation of the immune system (2023) · cites this paper as [201]
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Efficacy of Lenalidomide in Myelodysplastic Syndromes
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SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition
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Metadata
- Authors
- Basiorka, A. A., McGraw, K. L., Eksioglu, E. A., Chen, X., Johnson, J., Zhang, L., Zhang, Q., Irvine, B. A., Cluzeau, T., Sallman, D. A., Padron, E., Komrokji, R., Sokol, L., Coll, R. C., Robertson, A. A. B., Cooper, M. A., Cleveland, J. L., O’Neill, L. A., Wei, S., & List, A. F.
- Affiliations
- Cancer Biology Ph.D. Program, Department of Malignant Hematology,
- Department of Malignant Hematology,
- Department of Immunology,
- Analytic Microscopy Core Facility, and
- Department of Hematopathology, H. Lee Moffitt Cancer Center, Tampa, FL;
- Department of Hematology, Centre Hospitalier Universitaire de Nice, Nice, France;
- Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia;
- Department of Tumor Biology, H. Lee Moffitt Cancer Center, Tampa, FL; and
- Trinity Biomedical Sciences Institute, School of Biochemistry and Immunology, Trinity College Dublin, Dublin, Ireland
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2016-12-22
- Volume
- 128
- Issue
- 25
- Pages
- 2960-2975
- ISSN
- 0006-4971
- 1528-0020
- Cited by
- 348
- References
- 12
- Language
- en
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