Interieukin-6 regulation of prostate cancer cell growth

被引:225
作者
Culig, Z
Steiner, H
Bartsch, G
Hobisch, A
机构
[1] Innsbruck Med Univ, Dept Urol, A-6020 Innsbruck, Austria
[2] Gen Hosp Feldkirch, Dept Urol, Feldkirch, Austria
关键词
interleukin-6; prostate cancer; JAK/STAT; MAPK; androgen receptor;
D O I
10.1002/jcb.20477
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
Interleukin-6 (IL-6) is involved in regulation of immune reaction and cell growth and differentiation. It causes multifunctional responses ranging from inhibition of proliferation to promotion of cell survival. IL-6 effects may depend on experimental conditions such as passage numbers and serum composition. IL-6 signals in target tissues through the receptor that is composed of the ligand-binding and signai-transducing subunits. IL-6 is expressed in benign and malignant prostate tissue and the levels of the cytokine and its receptor increase during prostate carcinogenesis. IL-6 is considered a positive growth factor for most prostate cells. The only exemption seems to be the LNCaP cell line, in which IL-6 causes growth arrest and induces differentiation function. In contrast, IL-6 acts as an autocrine growth factor in the subline LNCaP-IL-6+ established after chronic treatment with IL-6. IL-6 is a candidate for targeted therapy in prostate cancer because of its association with morbidity. Activation of signaling pathways of Janus kinase/signal transducers and activators of transcription factors, mitogen-activated protein kinase (MAPK), and phosphaticlylinositol 3-kinase has been reported in various prostate cancer cell lines. IL-6 and the related cytokine oncostatin M induce activation of the androgen receptor (AR) in the absence of androgen. IL-6 is also involved in regulation of vascular endothelial growth factor expression as well as neuroendocrine differentiation in prostate. Anti-IL-6 antibodies showed an inhibitory effect on the PC-3 xenograft. However, the development of this therapy in prostate cancer is in early stages. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:497 / 505
页数:9
相关论文
共 78 条
[41]  
Lee SO, 2003, CLIN CANCER RES, V9, P370
[42]   NF-κB nuclear localization and its prognostic significance in prostate cancer [J].
Lessard, L ;
Mes-Masson, AM ;
Lamarre, L ;
Wall, L ;
Lattouf, JB ;
Saad, F .
BJU INTERNATIONAL, 2003, 91 (04) :417-420
[43]  
Li YW, 2002, CLIN CANCER RES, V8, P2369
[44]   Prostaglandin E2 stimulates prostatic intraepithelial neoplasia cell growth through activation of the interleukin-6/GP130/STAT-3 signaling pathway [J].
Liu, XH ;
Kirschenbaum, A ;
Lu, M ;
Yao, S ;
Klausner, A ;
Preston, C ;
Holland, JF ;
Levine, AC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (01) :249-255
[45]   Cross-talk between signal transducer and activator of transcription 3 and androgen receptor signaling in prostate carcinoma cells [J].
Matsuda, T ;
Junicho, A ;
Yamamoto, T ;
Kishi, H ;
Korkmaz, K ;
Saatcioglu, F ;
Fuse, H ;
Muraguchi, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 283 (01) :179-187
[46]  
Mora LB, 2002, CANCER RES, V62, P6659
[47]   Interleukin-6 induces G1 arrest through induction of p27Kip1, a cyclin-dependent kinase inhibitor, and neuron-like morphology in LNCaP prostate tumor cells [J].
Mori, S ;
Murakami-Mori, K ;
Bonavida, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (02) :609-614
[48]  
Mori S, 1999, ANTICANCER RES, V19, P1011
[49]  
Nakashima J, 2000, CLIN CANCER RES, V6, P2702
[50]   Potential mechanism for the effects of dexamethasone on growth of androgen-independent prostate cancer [J].
Nishimura, K ;
Nonomura, N ;
Satoh, E ;
Harada, Y ;
Nakayama, M ;
Tokizane, T ;
Fukui, T ;
Ono, Y ;
Inoue, H ;
Shin, M ;
Tsujimoto, Y ;
Takayama, H ;
Aozasa, K ;
Okuyama, A .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (22) :1739-1746