wjzhang_kyuu@gmu.edu.cn。
"],"authorList":[{"zuoZheDiZhiL_cn":["赣南医科大学第一临床医学院,江西 赣州 341000 ;赣南医科大学第一附属医院检验科,江西 赣州 341000 ;"],"deceased":false,"name_cn":"许中满","zuoZheDiZhiL_en":["The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China ;Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;"],"name_en":"Zhongman XU"},{"zuoZheDiZhiL_cn":["赣南医科大学第一临床医学院,江西 赣州 341000 ;赣南医科大学第一附属医院检验科,江西 赣州 341000 ;"],"deceased":false,"name_cn":"吴思铭","zuoZheDiZhiL_en":["The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China ;Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;"],"name_en":"Siming WU"},{"zuoZheDiZhiL_cn":["赣南医科大学第一临床医学院,江西 赣州 341000 ;赣南医科大学第一附属医院检验科,江西 赣州 341000 ;赣南医科大学第一附属医院精准医学中心,江西 赣州 341000 ;"],"deceased":false,"name_cn":"王晓玲","zuoZheDiZhiL_en":["The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China ;Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;Precision Medicine Center,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;"],"name_en":"Xiaoling WANG"},{"zuoZheDiZhiL_cn":["赣南医科大学第一临床医学院,江西 赣州 341000 ;赣南医科大学第一附属医院检验科,江西 赣州 341000 ;赣南医科大学第一附属医院精准医学中心,江西 赣州 341000 ;"],"deceased":false,"name_cn":"钟田雨","zuoZheDiZhiL_en":["The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China ;Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;Precision Medicine Center,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;"],"name_en":"Tianyu ZHONG"},{"zuoZheDiZhiL_cn":["赣南医科大学第一临床医学院,江西 赣州 341000 ;赣南医科大学第一附属医院检验科,江西 赣州 341000 ;赣南医科大学第一附属医院精准医学中心,江西 赣州 341000 ;赣南医科大学儿童白血病免疫治疗药物开发赣州市重点实验室,江西 赣州 341000 ;"],"deceased":false,"name_cn":"张文娟","email":"wjzhang_kyuu@gmu.edu.cn","zuoZheDiZhiL_en":["The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China ;Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;Precision Medicine Center,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China ;Ganzhou Key Laboratory of Immunotherapeutic Drugs Developing for Childhood Leukemia,Gannan Medical University,Ganzhou 341000,China ;"],"name_en":"Wenjuan ZHANG"}],"affList_en":["1.The First School of Clinical Medicine,Gannan Medical University,Ganzhou 341000,China
2.Laboratory Medicine,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China
3.Precision Medicine Center,First Affiliated Hospital of Gannan Medical University,Ganzhou 341000,China
4.Ganzhou Key Laboratory of Immunotherapeutic Drugs Developing for Childhood Leukemia,Gannan Medical University,Ganzhou 341000,China"],"fundList_cn":["国家自然科学基金(82203540)"],"affList_cn":["1.赣南医科大学第一临床医学院,江西 赣州 341000
2.赣南医科大学第一附属医院检验科,江西 赣州 341000
3.赣南医科大学第一附属医院精准医学中心,江西 赣州 341000
4.赣南医科大学儿童白血病免疫治疗药物开发赣州市重点实验室,江西 赣州 341000"],"article":{"keywordList_cn":["干扰素调节因子3","乳腺癌","Ⅰ型干扰素","免疫治疗"],"juan":"45","zhaiyao_cn":"

乳腺癌作为全球女性健康的重大挑战,其研究的重要性和紧迫性日益凸显。干扰素调节因子3(interferon regulatory factor 3,IRF3)属于人类干扰素调节因子(interferon regulatory factors,IRFs)家族的一员,是一个关键的转录因子。IRF3在天然免疫应答的信号传递过程中起着重要的调节作用。近年来研究揭示了IRF3在肿瘤免疫学领域的关键作用,特别是在乳腺癌中。IRF3不仅调节乳腺癌细胞的生长和凋亡,而且通过诱导Ⅰ型干扰素(type I interferons,IFN-Ⅰ)及其他重要细胞因子的产生,对肿瘤细胞的行为产生影响。然而,在乳腺癌中,IRF3的激活受到多种机制的抑制,这包括阻断IRF3依赖的细胞凋亡途径和通过调节微RNA表达来抑制干扰素基因刺激因子(stimulator of interferon genes,STING)等。在特定情况下,IRF3还可能促进乳腺癌发生及复发。本综述全面探讨了IRF3的基本特征、参与的信号通路、在乳腺癌发展中的作用及当前研究的最新进展,并总结了基于IRF3作用机制的潜在治疗方法。

","endNoteUrl_en":"http://xuebao.sdfmu.edu.cn/EN/article/getTxtFile.do?fileType=EndNote&id=660","reference":"
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26 Manetsch P, B?hi F, Nowak K, et al. PARP7-mediated ADP-ribosylation of FRA1 promotes cancer cell growth by repressing IRF1- and IRF3-dependent apoptosis[J]. Proc Natl Acad Sci U S A2023120(49): e2309047120.
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38 Demir Cetinkaya B, Biray Avci C. Molecular perspective on targeted therapy in breast cancer: a review of current status[J]. Med Oncol202239(10): 149.
39 Basu A, Ramamoorthi G, Jia YS, et al. Immunotherapy in breast cancer: current status and future directions[J]. Adv Cancer Res2019143: 295.
40 Lu X, Wang X, Cheng H, et al. Anti-triple-negative breast cancer metastasis efficacy and molecular mechanism of the Sting agonist for innate immune pathway[J]. Ann Med202355(1): 2210845.
41 Takahashi-Ruiz L, Fermaintt CS, Wilkinson NJ, et al. The microtubule destabilizer eribulin synergizes with Sting agonists to promote antitumor efficacy in Triple-Negative breast cancer models[J]. Cancers (Basel)202214(23): 5962.
42 Yeo SK, Haas M, Manupati K, et al. AZI2 mediates TBK1 activation at unresolved selective autophagy cargo receptor complexes with implications for CD8 T-cell infiltration in breast cancer[J]. Autophagy202420(3): 525.
43 Liu X, He B. Selective editing of herpes simplex virus 1 enables interferon induction and viral replication that destroy malignant cells[J]. J Virol201993(2): e01761.
44 Brown MC, Mosaheb MM, Mohme M, et al. Viral infection of cells within the tumor microenvironment mediates antitumor immunotherapy via selective TBK1-IRF3 signaling[J]. Nat Commun202112(1): 1858.
45 Long Y, Guo JX, Chen JL, et al. GPR162 activates Sting dependent DNA damage pathway as a novel tumor suppressor and radiation sensitizer[J]. Signal Transduct Target Ther20238(1): 48.
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As a significant challenge to women's health globally, the research of breast cancer has shown increasingly prominence and urgency. Interferon regulatory factor 3 (IRF3), a member of the human interferon regulatory factor (IRF) family, serves as a crucial transcription factor. IRF3 plays a significant role in regulating the signal transduction process of the innate immune response. Recent research advancements have discovered IRF3’s pivotal role in the field of tumor immunology, particularly its significant impact on breast cancer. IRF3 regulates the growth and apoptosis of breast cancer cells and influences tumor cell behavior by inducing the production of type I interferons (IFN-I) and other critical cytokines. However, in breast cancer, the activation of IRF3 is suppressed by various mechanisms, including the obstruction of IRF3-dependent apoptosis pathways and the inhibition of stimulator of interferon genes (STING) expression through the modulation of microRNA expression. Under certain circumstances, IRF3 may also promote the occurrence and recurrence of breast cancer. This review comprehensively explores the fundamental characteristics of IRF3, its signaling pathways, roles in developing breast cancer, the latest research progress, and summarizes potential therapeutic strategies based on the mechanism of action of IRF3.

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IRF3在乳腺癌中的研究进展

许中满, 吴思铭, 王晓玲, 钟田雨, 张文娟

betway必威登陆网址 (betway.com )学报››2024, Vol. 45››Issue (5): 315-320.

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PDF(461 KB)
betway必威登陆网址 (betway.com )学报 ›› 2024, Vol. 45 ›› Issue (5) : 315-320. DOI: 10.3969/j.issn.2097-0005.2024.05.012
综述

IRF3在乳腺癌中的研究进展

    作者信息 +

    Advances in research on IRF3 in breast cancer

      Author information +
      文章历史 +

      摘要

      乳腺癌作为全球女性健康的重大挑战,其研究的重要性和紧迫性日益凸显。干扰素调节因子3(interferon regulatory factor 3,IRF3)属于人类干扰素调节因子(interferon regulatory factors,IRFs)家族的一员,是一个关键的转录因子。IRF3在天然免疫应答的信号传递过程中起着重要的调节作用。近年来研究揭示了IRF3在肿瘤免疫学领域的关键作用,特别是在乳腺癌中。IRF3不仅调节乳腺癌细胞的生长和凋亡,而且通过诱导Ⅰ型干扰素(type I interferons,IFN-Ⅰ)及其他重要细胞因子的产生,对肿瘤细胞的行为产生影响。然而,在乳腺癌中,IRF3的激活受到多种机制的抑制,这包括阻断IRF3依赖的细胞凋亡途径和通过调节微RNA表达来抑制干扰素基因刺激因子(stimulator of interferon genes,STING)等。在特定情况下,IRF3还可能促进乳腺癌发生及复发。本综述全面探讨了IRF3的基本特征、参与的信号通路、在乳腺癌发展中的作用及当前研究的最新进展,并总结了基于IRF3作用机制的潜在治疗方法。

      Abstract

      As a significant challenge to women's health globally, the research of breast cancer has shown increasingly prominence and urgency. Interferon regulatory factor 3 (IRF3), a member of the human interferon regulatory factor (IRF) family, serves as a crucial transcription factor. IRF3 plays a significant role in regulating the signal transduction process of the innate immune response. Recent research advancements have discovered IRF3’s pivotal role in the field of tumor immunology, particularly its significant impact on breast cancer. IRF3 regulates the growth and apoptosis of breast cancer cells and influences tumor cell behavior by inducing the production of type I interferons (IFN-I) and other critical cytokines. However, in breast cancer, the activation of IRF3 is suppressed by various mechanisms, including the obstruction of IRF3-dependent apoptosis pathways and the inhibition of stimulator of interferon genes (STING) expression through the modulation of microRNA expression. Under certain circumstances, IRF3 may also promote the occurrence and recurrence of breast cancer. This review comprehensively explores the fundamental characteristics of IRF3, its signaling pathways, roles in developing breast cancer, the latest research progress, and summarizes potential therapeutic strategies based on the mechanism of action of IRF3.

      关键词

      干扰素调节因子3/乳腺癌/Ⅰ型干扰素/免疫治疗

      Key words

      IRF3/breast cancer/type I interferon/immunotherapy

      引用本文

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      许中满, 吴思铭, 王晓玲, 钟田雨, 张文娟.IRF3在乳腺癌中的研究进展[J]. betway必威登陆网址 (betway.com )学报. 2024, 45(5): 315-320 https://doi.org/10.3969/j.issn.2097-0005.2024.05.012
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