IRF4 as an Oncogenic Master Transcription Factor

被引:24
|
作者
Wong, Regina Wan Ju [1 ]
Ong, Jolynn Zu Lin [1 ]
Theardy, Madelaine Skolastika [1 ]
Sanda, Takaomi [1 ,2 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117599, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore 117599, Singapore
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
IRF4; oncogene; transcription factor; mature lymphoid neoplasms; NF-KAPPA-B; GERMINAL CENTER B; INTERFERON REGULATORY FACTOR-4; MUM1/IRF4 PROTEIN EXPRESSION; STIMULATED RESPONSE ELEMENT; SEQUENCE BINDING-PROTEIN; CELL LYMPHOMA; FACTOR FAMILY; MATURE B; DIFFERENTIAL EXPRESSION;
D O I
10.3390/cancers14174314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. 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-kappa B 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.
引用
收藏
页数:13
相关论文
共 50 条
  • [21] The transcription factor IRF4 is essential for TCR affinity–mediated metabolic programming and clonal expansion of T cells
    Kevin Man
    Maria Miasari
    Wei Shi
    Annie Xin
    Darren C Henstridge
    Simon Preston
    Marc Pellegrini
    Gabrielle T Belz
    Gordon K Smyth
    Mark A Febbraio
    Stephen L Nutt
    Axel Kallies
    Nature Immunology, 2013, 14 : 1155 - 1165
  • [22] Shared and Distinct Functions of the Transcription Factors IRF4 and IRF8 in Myeloid Cell Development
    Yamamoto, Michio
    Kato, Takayuki
    Hotta, Chie
    Nishiyama, Akira
    Kurotaki, Daisuke
    Yoshinari, Masahiro
    Takami, Masamichi
    Ichino, Motohide
    Nakazawa, Masatoshi
    Matsuyama, Toshifumi
    Kamijo, Ryutaro
    Kitagawa, Seiichi
    Ozato, Keiko
    Tamura, Tomohiko
    PLOS ONE, 2011, 6 (10):
  • [23] Quality of TCR signaling determined by differential affinities of enhancers for the composite BATF–IRF4 transcription factor complex
    Arifumi Iwata
    Vivek Durai
    Roxane Tussiwand
    Carlos G Briseño
    Xiaodi Wu
    Gary E Grajales-Reyes
    Takeshi Egawa
    Theresa L Murphy
    Kenneth M Murphy
    Nature Immunology, 2017, 18 : 563 - 572
  • [24] What on "Irf" Is This Gene 4? Irf4 Transcription-Factor-Dependent Dendritic Cells Are Required for T Helper 2 Cell Responses in Murine Skin
    Flutter, Barry
    Nestle, Frank O.
    IMMUNITY, 2013, 39 (04) : 625 - 627
  • [25] Ablation of Transcription Factor IRF4 Promotes Transplant Acceptance by Driving Allogenic CD4+ T Cell Dysfunction
    Wu, Jie
    Zhang, Hedong
    Shi, Xiaomin
    Xiao, Xiang
    Fan, Yihui
    Minze, Laurie J.
    Wang, Jin
    Ghobrial, Rafik M.
    Xia, Jiahong
    Sciammas, Roger
    Li, Xian C.
    Chen, Wenhao
    IMMUNITY, 2017, 47 (06) : 1114 - +
  • [26] Ablation of Transcription Factor IRF4 Promotes Transplant Acceptance by Driving Allogenic CD4+ T Cell Dysfunction
    Muller, Elmi
    TRANSPLANTATION, 2018, 102 (04) : 541 - 542
  • [27] Transcription Factor IRF4 Regulates Germinal Center Cell Formation through a B Cell-Intrinsic Mechanism
    Willis, Simon N.
    Good-Jacobson, Kim L.
    Curtis, Joan
    Light, Amanda
    Tellier, Julie
    Shi, Wei
    Smyth, Gordon K.
    Tarlinton, David M.
    Belz, Gabrielle T.
    Corcoran, Lynn M.
    Kallies, Axel
    Nutt, Stephen L.
    JOURNAL OF IMMUNOLOGY, 2014, 192 (07): : 3200 - 3206
  • [28] IRF4 Mediates the Oncogenic Effects of STAT3 in Anaplastic Large Cell Lymphomas
    Bandini, Cecilia
    Pupuleku, Aldi
    Spaccarotella, Elisa
    Pellegrino, Elisa
    Wang, Rui
    Vitale, Nicoletta
    Duval, Carlotta
    Cantarella, Daniela
    Rinaldi, Andrea
    Provero, Paolo
    Di Cunto, Ferdinando
    Medico, Enzo
    Bertoni, Francesco
    Inghirami, Giorgio
    Piva, Roberto
    CANCERS, 2018, 10 (01):
  • [29] Transcription factor IRF4 determines germinal center formation through follicular T-helper cell differentiation
    Bollig, Nadine
    Bruestle, Anne
    Kellner, Kerstin
    Ackermann, Waltraud
    Abass, Elfadil
    Raifer, Hartmann
    Camara, Baerbel
    Brendel, Cornelia
    Giel, Gavin
    Bothur, Evita
    Huber, Magdalena
    Paul, Christoph
    Elli, Alexandra
    Kroczek, Richard A.
    Nurieva, Roza
    Dong, Chen
    Jacob, Ralf
    Mak, Tak W.
    Lohoff, Michael
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (22) : 8664 - 8669
  • [30] The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells
    Man, Kevin
    Miasari, Maria
    Shi, Wei
    Xin, Annie
    Henstridge, Darren C.
    Preston, Simon
    Pellegrini, Marc
    Belz, Gabrielle T.
    Smyth, Gordon K.
    Febbraio, Mark A.
    Nutt, Stephen L.
    Kallies, Axel
    NATURE IMMUNOLOGY, 2013, 14 (11) : 1155 - U79