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IRF4 as an Oncogenic Master Transcription Factor
SIMPLE SUMMARY: Master transcription factors regulate essential developmental processes and cellular maintenance that characterize cell identity. Many of them also serve as oncogenes when aberrantly expressed or activated. IRF4 is one of prime examples of oncogenic master transcription factors that...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454692/ https://www.ncbi.nlm.nih.gov/pubmed/36077849 http://dx.doi.org/10.3390/cancers14174314 |
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author | Wong, Regina Wan Ju Ong, Jolynn Zu Lin Theardy, Madelaine Skolastika Sanda, Takaomi |
author_facet | Wong, Regina Wan Ju Ong, Jolynn Zu Lin Theardy, Madelaine Skolastika Sanda, Takaomi |
author_sort | Wong, Regina Wan Ju |
collection | PubMed |
description | SIMPLE SUMMARY: Master transcription factors regulate essential developmental processes and cellular maintenance that characterize cell identity. Many of them also serve as oncogenes when aberrantly expressed or activated. IRF4 is one of prime examples of oncogenic master transcription factors that has been implicated in various mature lymphoid neoplasms. IRF4 forms unique regulatory circuits and induces oncogenic transcription programs through the interactions with upstream pathways and binding partners. ABSTRACT: IRF4 is a transcription factor in the interferon regulatory factor (IRF) family. Since the discovery of this gene, various research fields including immunology and oncology have highlighted the unique characteristics and the importance of IRF4 in several biological processes that distinguish it from other IRF family members. In normal lymphocyte development and immunity, IRF4 mediates critical immune responses via interactions with upstream signaling pathways, such as the T-cell receptor and B-cell receptor pathways, as well as their binding partners, which are uniquely expressed in each cell type. On the other hand, IRF4 acts as an oncogene in various mature lymphoid neoplasms when abnormally expressed. IRF4 induces several oncogenes, such as MYC, as well as genes that characterize each cell type by utilizing its ability as a master regulator of immunity. IRF4 and its upstream factor NF-κB form a transcriptional regulatory circuit, including feedback and feedforward loops, to maintain the oncogenic transcriptional program in malignant lymphoid cells. In this review article, we provide an overview of the molecular functions of IRF4 in mature lymphoid neoplasms and highlight its upstream and downstream pathways, as well as the regulatory circuits mediated by IRF4. |
format | Online Article Text |
id | pubmed-9454692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94546922022-09-09 IRF4 as an Oncogenic Master Transcription Factor Wong, Regina Wan Ju Ong, Jolynn Zu Lin Theardy, Madelaine Skolastika Sanda, Takaomi Cancers (Basel) Review SIMPLE SUMMARY: Master transcription factors regulate essential developmental processes and cellular maintenance that characterize cell identity. Many of them also serve as oncogenes when aberrantly expressed or activated. IRF4 is one of prime examples of oncogenic master transcription factors that has been implicated in various mature lymphoid neoplasms. IRF4 forms unique regulatory circuits and induces oncogenic transcription programs through the interactions with upstream pathways and binding partners. ABSTRACT: IRF4 is a transcription factor in the interferon regulatory factor (IRF) family. Since the discovery of this gene, various research fields including immunology and oncology have highlighted the unique characteristics and the importance of IRF4 in several biological processes that distinguish it from other IRF family members. In normal lymphocyte development and immunity, IRF4 mediates critical immune responses via interactions with upstream signaling pathways, such as the T-cell receptor and B-cell receptor pathways, as well as their binding partners, which are uniquely expressed in each cell type. On the other hand, IRF4 acts as an oncogene in various mature lymphoid neoplasms when abnormally expressed. IRF4 induces several oncogenes, such as MYC, as well as genes that characterize each cell type by utilizing its ability as a master regulator of immunity. IRF4 and its upstream factor NF-κB form a transcriptional regulatory circuit, including feedback and feedforward loops, to maintain the oncogenic transcriptional program in malignant lymphoid cells. In this review article, we provide an overview of the molecular functions of IRF4 in mature lymphoid neoplasms and highlight its upstream and downstream pathways, as well as the regulatory circuits mediated by IRF4. MDPI 2022-09-02 /pmc/articles/PMC9454692/ /pubmed/36077849 http://dx.doi.org/10.3390/cancers14174314 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Wong, Regina Wan Ju Ong, Jolynn Zu Lin Theardy, Madelaine Skolastika Sanda, Takaomi IRF4 as an Oncogenic Master Transcription Factor |
title | IRF4 as an Oncogenic Master Transcription Factor |
title_full | IRF4 as an Oncogenic Master Transcription Factor |
title_fullStr | IRF4 as an Oncogenic Master Transcription Factor |
title_full_unstemmed | IRF4 as an Oncogenic Master Transcription Factor |
title_short | IRF4 as an Oncogenic Master Transcription Factor |
title_sort | irf4 as an oncogenic master transcription factor |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454692/ https://www.ncbi.nlm.nih.gov/pubmed/36077849 http://dx.doi.org/10.3390/cancers14174314 |
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