JAK-STAT signaling in cancer: From cytokines to non-coding genome

被引:180
作者
Pencik, Jan [1 ,2 ,3 ]
Ha Thi Thanh Pham [3 ,4 ]
Schmoellerl, Johannes [3 ]
Javaheri, Tahereh [3 ,4 ]
Schlederer, Michaela [1 ,3 ,6 ]
Culig, Zoran [5 ]
Merkel, Olaf [1 ]
Moriggl, Richard [3 ,4 ]
Grebien, Florian [3 ]
Kenner, Lukas [1 ,3 ,6 ]
机构
[1] Med Univ Vienna, Clin Inst Pathol, AT-1090 Vienna, Austria
[2] Dept Biomed Imaging & Image Guided Therapy, Div Nucl Med, A-1090 Vienna, Austria
[3] Med Univ Vienna, Ludwig Boltzmann Inst Canc Res, A-1090 Vienna, Austria
[4] Med Univ Vienna, Univ Vet Med Vienna, Inst Anim Breeding & Genet, A-1210 Vienna, Austria
[5] Med Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria
[6] Univ Vet Med Vienna, Dept Pathol Lab Anim, AT-1210 Vienna, Austria
基金
欧盟地平线“2020”; 奥地利科学基金会;
关键词
JAK/STAT signaling; Non-coding RNAs; Prostate cancer; Hematopoietic malignancies; Sarcomas; TUMOR-ASSOCIATED MACROPHAGES; CELL-CYCLE ARREST; PROSTATE-CANCER; CONSTITUTIVE ACTIVATION; TYROSINE KINASE; POOR-PROGNOSIS; SMALL-MOLECULE; EWING SARCOMA; BREAST-CANCER; ESSENTIAL THROMBOCYTHEMIA;
D O I
10.1016/j.cyto.2016.06.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the past decades, studies of the Janus kinases (JAKs) and signal transducers and activators of transcription (STATs) signaling have uncovered highly conserved programs linking cytokine signaling to the regulation of essential cellular mechanisms such as proliferation, invasion, survival, inflammation and immunity. Inhibitors of the JAK/STAT pathway are used for treatment of autoimmune diseases, such as rheumatoid arthritis or psoriasis. Aberrant JAK/STAT signaling has been identified to contribute to cancer progression and metastatic development. Targeting of JAK/STAT pathway is currently one of the most promising therapeutic strategies in prostate cancer (PCa), hematopoietic malignancies and sarcomas. Notably, newly identified regulators of JAK/STAT signaling, the non-coding RNAs transcripts and their role as important targets and potential clinical biomarkers are highlighted in this review. In addition to the established role of the JAK/STAT signaling pathway in traditional cytokine signaling the non-coding RNAs add yet another layer of hidden regulation and function. Understanding the crosstalk of non-coding RNA with JAK/STAT signaling in cancer is of critical importance and may result in better patient stratification not only in terms of prognosis but also in the context of therapy. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:26 / 36
页数:11
相关论文
共 203 条
[1]   Control of senescence by CXCR2 and its ligands [J].
Acosta, Juan C. ;
O'Loghlen, Ana ;
Banito, Ana ;
Raguz, Selina ;
Gil, Jesus .
CELL CYCLE, 2008, 7 (19) :2956-2959
[2]   Chemokine signaling via the CXCR2 receptor reinforces senescence [J].
Acosta, Juan C. ;
O'Loghlen, Ana ;
Banito, Ana ;
Guijarro, Maria V. ;
Augert, Arnaud ;
Raguz, Selina ;
Fumagalli, Marzia ;
Da Costa, Marco ;
Brown, Celia ;
Popov, Nikolay ;
Takatsu, Yoshihiro ;
Melamed, Jonathan ;
di Fagagna, Fabrizio d'Adda ;
Bernard, David ;
Hernando, Eva ;
Gil, Jesus .
CELL, 2008, 133 (06) :1006-1018
[3]   MAPK and JAK/STAT pathways targeted by miR-23a and miR-23b in prostate cancer: computational and in vitro approaches [J].
Aghaee-Bakhtiari, Seyed Hamid ;
Arefian, Ehsan ;
Naderi, Mahmood ;
Noorbakhsh, Farshid ;
Nodouzi, Vahideh ;
Asgari, Mojgan ;
Fard-Esfahani, Pezhman ;
Mahdian, Reza ;
Soleimani, Masoud .
TUMOR BIOLOGY, 2015, 36 (06) :4203-4212
[4]   Phosphoproteomic Profiling Reveals IL6-Mediated Paracrine Signaling within the Ewing Sarcoma Family of Tumors [J].
Anderson, Jennifer L. ;
Titz, Bjoern ;
Akiyama, Ryan ;
Komisopoulou, Evangelia ;
Park, Ann ;
Tap, William D. ;
Graeber, Thomas G. ;
Denny, Christopher T. .
MOLECULAR CANCER RESEARCH, 2014, 12 (12) :1740-1754
[5]   Pediatric sarcomas: translating molecular pathogenesis of disease to novel therapeutic possibilities [J].
Anderson, Jennifer L. ;
Denny, Christopher T. ;
Tap, William D. ;
Federman, Noah .
PEDIATRIC RESEARCH, 2012, 72 (02) :112-121
[6]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[7]  
Antonescu CR, 2001, CLIN CANCER RES, V7, P3977
[8]   Constitutive activation of STAT5 by a point mutation in the SH2 domain [J].
Ariyoshi, K ;
Nosaka, T ;
Yamada, K ;
Onishi, M ;
Oka, Y ;
Miyajima, A ;
Kitamura, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24407-24413
[9]   Stat3 Mediates Expression of Autotaxin in Breast Cancer [J].
Azare, Janeen ;
Doane, Ashley ;
Leslie, Kenneth ;
Chang, Qing ;
Berishaj, Marjan ;
Nnoli, Jennifer ;
Mark, Kevin ;
Al-Ahmadie, Hikmat ;
Gerald, William ;
Hassimi, Maryam ;
Viale, Agnes ;
Stracke, Mary ;
Lyden, David ;
Bromberg, Jacqueline .
PLOS ONE, 2011, 6 (11)
[10]   Potent and Selective Inhibition of Polycythemia by the Quinoxaline JAK2 Inhibitor NVP-BSK805 [J].
Baffert, Fabienne ;
Regnier, Catherine H. ;
De Pover, Alain ;
Pissot-Soldermann, Carole ;
Tavares, Gisele A. ;
Blasco, Francesca ;
Brueggen, Josef ;
Chene, Patrick ;
Drueckes, Peter ;
Erdmann, Dirk ;
Furet, Pascal ;
Gerspacher, Marc ;
Lang, Marc ;
Ledieu, David ;
Nolan, Lynda ;
Ruetz, Stephan ;
Trappe, Joerg ;
Vangrevelinghe, Eric ;
Wartmann, Markus ;
Wyder, Lorenza ;
Hofmann, Francesco ;
Radimerski, Thomas .
MOLECULAR CANCER THERAPEUTICS, 2010, 9 (07) :1945-1955