MicroRNAs and STAT interplay

被引:92
作者
Kohanbash, Gary [1 ,2 ]
Okada, Hideho [2 ,3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Infect Dis & Microbiol, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Inst Canc, Brain Tumor Program, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Dept Neurol Surg, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Sch Med, Dept Surg, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
miR-17-92; microRNA; STATs; Cytokine; Chemokine; T cells; B cells; Malignancy; SIGNAL TRANSDUCER; CONFERS TUMORIGENICITY; MIR-17-92; CLUSTER; T-CELLS; EXPRESSION; TRANSCRIPTION; INTERFERON; ACTIVATOR; PROTEIN; FAMILY;
D O I
10.1016/j.semcancer.2011.12.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA (miR) are emerging as important gene expression regulators often involved in a variety of pathogenesis such as cancers and autoimmunity. Signal transducers and activators of transcription (STAT) proteins are the principle signaling proteins for many cytokines and growth factors, thereby play a critical role in regulating immune cell homeostasis, differentiation and cellular functions. In this review, we discuss recent advances in the field demonstrating active interactions between STATs and miRs, with our primary focus on the promotion and inhibition of immune cells and cancer. Additionally, we review the reciprocal regulations between STATs and miR, and discuss how we can use this knowledge in the context of diseases. For example, recent findings related to STAT1 and miR-155 support the presence of a positive feedback loop of miR-155 and STAT1 in response to inflammatory signals or infection. STAT3 is known to play critical roles in tumorigenesis and cancer-induced immunosuppression. There is a growing body of evidence demonstrating that STAT3 directly activates miR-21, one of miRs that promote cancer cell survival and proliferation. While some miRs directly regulate STATs, there are findings demonstrating indirect STAT regulation by miRs also mediate important biological mechanisms. Therefore, further research is warranted to elucidate significant contributions made by direct and indirect miR-STAT mechanisms. As we learn more about miR pathways, we gain the opportunity to manipulate them in cancer cells to slow down growth or increase their susceptibility anti-tumor immunity. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:70 / 75
页数:6
相关论文
共 76 条
  • [1] Functional roles of STAT family proteins: Lessons from knockout mice
    Akira, S
    [J]. STEM CELLS, 1999, 17 (03) : 138 - 146
  • [2] Interferon-alpha in tumor immunity and immunotherapy
    Belardelli, F
    Ferrantini, M
    Proietti, E
    Kirkwood, JM
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2002, 13 (02) : 119 - 134
  • [3] Interleukin-6 Modulates the Expression of the Bone Morphogenic Protein Receptor Type II Through a Novel STAT3-microRNA Cluster 17/92 Pathway
    Brock, Matthias
    Trenkmann, Michelle
    Gay, Renate E.
    Michel, Beat A.
    Gay, Steffen
    Fischler, Manuel
    Ulrich, Silvia
    Speich, Rudolf
    Huber, Lars C.
    [J]. CIRCULATION RESEARCH, 2009, 104 (10) : 1184 - U139
  • [4] miR-17 family of microRNAs controls FGF10-mediated embryonic lung epithelial branching morphogenesis through MAPK14 and STAT3 regulation of E-Cadherin distribution
    Carraro, Gianni
    El-Hashash, Ahmed
    Guidolin, Diego
    Tiozzo, Caterina
    Turcatel, Gianluca
    Young, Brittany M.
    De langhe, Stijn P.
    Bellusci, Saverio
    Shi, Wei
    Parnigotto, Pier Paolo
    Warburton, David
    [J]. DEVELOPMENTAL BIOLOGY, 2009, 333 (02) : 238 - 250
  • [5] miR-20b Modulates VEGF Expression by Targeting HIF-1α and STAT3 in MCF-7 Breast Cancer Cells
    Cascio, Sandra
    D'Andrea, Aleco
    Ferla, Rita
    Surmacz, Eva
    Gulotta, Eliana
    Amodeo, Valeria
    Bazan, Viviana
    Gebbi, Nicola
    Russo, Antonio
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2010, 224 (01) : 242 - 249
  • [6] MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells
    Chan, JA
    Krichevsky, AM
    Kosik, KS
    [J]. CANCER RESEARCH, 2005, 65 (14) : 6029 - 6033
  • [7] miR-17-92 cluster microRNAs confers tumorigenicity in multiple myeloma
    Chen, Lijuan
    Li, Chunming
    Zhang, Run
    Gao, Xiao
    Qu, Xiaoyan
    Zhao, Min
    Qiao, Chun
    Xu, Jiaren
    Li, Jianyong
    [J]. CANCER LETTERS, 2011, 309 (01) : 62 - 70
  • [8] Characterization of the human STAT5A and STAT5B promoters:: evidence of a positive and negative mechanism of transcriptional regulation
    Crispi, S
    Sanzari, E
    Monfregola, J
    De Felice, N
    Fimiani, G
    Ambrosio, R
    D'Urso, M
    Ursini, MV
    [J]. FEBS LETTERS, 2004, 562 (1-3): : 27 - 34
  • [9] microRNA-222 Controls Neovascularization by Regulating Signal Transducer and Activator of Transcription 5A Expression
    Dentelli, Patrizia
    Rosso, Arturo
    Orso, Francesca
    Olgasi, Cristina
    Taverna, Daniela
    Brizzi, Maria Felice
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2010, 30 (08) : 1562 - U125
  • [10] MicroRNA Let-7a Inhibits Proliferation of Human Prostate Cancer Cells In Vitro and In Vivo by Targeting E2F2 and CCND2
    Dong, Qingchuan
    Meng, Ping
    Wang, Tao
    Qin, Weiwei
    Qin, Weijun
    Wang, Fuli
    Yuan, Jianlin
    Chen, Zhinan
    Yang, Angang
    Wang, He
    [J]. PLOS ONE, 2010, 5 (04):