The CCAAT/Enhancer-Binding Protein Family: Its Roles in MDSC Expansion and Function
Immunosuppressive cells have been highlighted in research due to their roles in tumor progression and treatment failure. Myeloid-derived suppressor cells (MDSCs) are among the major immunosuppressive cell populations in the tumor microenvironment, and transcription factors (TFs) are likely involved...
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Published in | Frontiers in immunology Vol. 10; p. 1804 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
31.07.2019
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Subjects | |
Online Access | Get full text |
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Summary: | Immunosuppressive cells have been highlighted in research due to their roles in tumor progression and treatment failure. Myeloid-derived suppressor cells (MDSCs) are among the major immunosuppressive cell populations in the tumor microenvironment, and transcription factors (TFs) are likely involved in MDSC expansion and activation. As key regulatory TFs, members of the CCAAT/enhancer-binding protein (C/EBP) family possibly modulate many biological processes, including cell growth, differentiation, metabolism, and death. Current evidence suggests that C/EBPs maintain critical regulation of MDSCs and are involved in the differentiation and function of MDSCs within the tumor microenvironment. To better understand the MDSC-associated transcriptional network and identify new therapy targets, we herein review recent findings about the C/EBP family regarding their participation in the expansion and function of MDSCs. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Molecular Innate Immunity, a section of the journal Frontiers in Immunology Reviewed by: Nagarkatti Prakash, University of South Carolina, United States; Ilaria Marigo, Istituto Oncologico Veneto (IRCCS), Italy Edited by: Jan Fric, International Clinical Research Center (FNUSA-ICRC), Czechia |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2019.01804 |