Crosstalk between cancer and immune cells: role of STAT3 in the tumour microenvironment

被引:1485
作者
Yu, Hua [1 ]
Kortylewski, Marcin
Pardoll, Drew
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Div Canc Immunotherapeut & Tumour Immunol, Duarte, CA 91010 USA
[2] Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune cells in the tumour microenvironment not only fail to mount an effective anti-tumour immune response, but also interact intimately with the transformed cells to promote oncogenesis actively. Signal transducer and activator of transcription 3 (STAT3), which is a point of convergence for numerous oncogenic signalling pathways, is constitutively activated both in tumour cells and in immune cells in the tumour microenvironment. Constitutively activated STAT3 inhibits the expression of mediators necessary for immune activation against tumour cells. Furthermore, STAT3 activity promotes the production of immunosuppressive factors that activate STAT3 in diverse immune-cell subsets, altering gene-expression programmes and, thereby, restraining anti-tumour immune responses. As such, STAT3 propagates several levels of crosstalk between tumour cells and their immunological microenvironment, leading to tumour-induced immunosuppression. Consequently, STAT3 has emerged as a promising target for cancer immunotherapy.
引用
收藏
页码:41 / 51
页数:11
相关论文
共 121 条
[1]   Suppressors of cytokine signalling (SOCS) in the immune system [J].
Alexander, WS .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (06) :410-416
[2]   Induced somatic inactivation of STAT3 in mice triggers the development of a fulminant form of enterocolitis [J].
Alonzi, T ;
Newton, IP ;
Bryce, PJ ;
Di Carlo, E ;
Lattanzio, G ;
Tripodi, M ;
Musiani, P ;
Poli, V .
CYTOKINE, 2004, 26 (02) :45-56
[3]   Selective inhibition of STAT3 induces apoptosis and G1 cell cycle arrest in ALK-positive anaplastic large cell lymphoma [J].
Amin, HM ;
McDonnell, TJ ;
Ma, YP ;
Lin, Q ;
Fujio, Y ;
Kunisada, K ;
Leventaki, V ;
Das, P ;
Rassidakis, GZ ;
Cutler, C ;
Medeiros, LJ ;
Lai, R .
ONCOGENE, 2004, 23 (32) :5426-5434
[4]   IL-2 overcomes the unresponsiveness but fails to reverse the regulatory function of antigen-induced T regulatory cells [J].
Anderson, PO ;
Sundstedt, A ;
Yazici, Z ;
Minaee, S ;
Woolf, R ;
Nicolson, K ;
Whitley, N ;
Li, L ;
Li, SL ;
Wraith, DC ;
Wang, P .
JOURNAL OF IMMUNOLOGY, 2005, 174 (01) :310-319
[5]   Essential role for STAT5 signaling in CD25+CD4+ regulatory T cell homeostasis and the maintenance of self-tolerance [J].
Antov, A ;
Yang, L ;
Vig, M ;
Baltimore, D ;
Van Parijs, L .
JOURNAL OF IMMUNOLOGY, 2003, 171 (07) :3435-3441
[6]   Inhibition of STAT3 signaling induces apoptosis and decreases survivin expression in primary effusion lymphoma [J].
Aoki, Y ;
Feldman, GM ;
Tosato, G .
BLOOD, 2003, 101 (04) :1535-1542
[7]   Cancer: What should be done? [J].
Bishop, JM .
SCIENCE, 1997, 278 (5340) :995-995
[8]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[9]   Cancer immunotherapy: A treatment for the masses [J].
Blattman, JN ;
Greenberg, PD .
SCIENCE, 2004, 305 (5681) :200-205
[10]   Stat3-mediated Myc expression is required for Src transformation and PDGF-induced mitogenesis [J].
Bowman, T ;
Broome, MA ;
Sinibaldi, D ;
Wharton, W ;
Pledger, WJ ;
Sedivy, JM ;
Irby, R ;
Yeatman, T ;
Courtneidge, SA ;
Jove, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (13) :7319-7324