Interleukin-6 is a potent inducer of S100P, which is up-regulated in androgen-refractory and metastatic prostate cancer

被引:37
作者
Hammacher, A
Thompson, EW
Williams, ED
机构
[1] Univ Melbourne, Bernard O Brien Inst Microsurg, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, St Vincents Hosp, Dept Surg, Fitzroy, Vic 3065, Australia
基金
英国医学研究理事会;
关键词
S100P; interleukin-6; prostate cancer; gp130; Cyr61/CCN1;
D O I
10.1016/j.biocel.2004.07.011
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
Elevated circulating interleukin-6 (IL6) and up-regulated S100P in prostate cancer (PCa) specimens correlate independently with progression to androgen-independent and metastatic PCa. The cause of up-regulated S100P levels in advanced PCa remains to be determined. We investigated the possibility that IL6 is an inducer of S100P. Determination of mRNA and protein levels by real-time PCR and Western blotting revealed that IL6 is a more potent inducer of S100P than the synthetic androgen, R1881, in the LNCaP/C4-2B model of PCa progression. IL6 did not require androgen to induce S100P in these cells, which express a functional androgen receptor (AR). Like R1881, IL6 was unable to induce S100P in PC3 cells that lack a functional AR. IL6 did not strongly induce the AR-dependent genes PSA and KLK2 and, contrary to R1881, down-regulated Cyr61/CCN1, a potential marker that is down-regulated in PCa. Epidermal growth factor (EGF), which like IL6 is a non-androgen activator of the AR, did not induce S100P. The data identifies a unique gene-induction profile for IL6 and suggests that IL6 may require a functional AR for S100P induction. A link between elevated IL6 and up-regulated S100P in androgen-refractory and metastatic PCa is postulated. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:442 / 450
页数:9
相关论文
共 37 条
[1]  
Abrahamsson PA, 1999, PROSTATE, V39, P135, DOI 10.1002/(SICI)1097-0045(19990501)39:2<135::AID-PROS9>3.0.CO
[2]  
2-S
[3]   Elevated levels of circulating interleukin-6 and transforming growth factor-β1 in patients with metastatic prostatic carcinoma [J].
Adler, HL ;
McCurdy, MA ;
Kattan, MW ;
Timme, TL ;
Scardino, PT ;
Thompson, TC .
JOURNAL OF UROLOGY, 1999, 161 (01) :182-187
[4]  
Amler LC, 2000, CANCER RES, V60, P6134
[5]   S100P stimulates cell proliferation and survival via receptor for activated glycation end products (RAGE) [J].
Arumugam, T ;
Simeone, DM ;
Schmidt, AM ;
Logsdon, CD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (07) :5059-5065
[6]  
Averboukh L, 1996, PROSTATE, V29, P350
[7]   S100P, A NOVEL CA2+-BINDING PROTEIN FROM HUMAN PLACENTA - CDNA CLONING, RECOMBINANT PROTEIN EXPRESSION AND CA2+ BINDING-PROPERTIES [J].
BECKER, T ;
GERKE, V ;
KUBE, E ;
WEBER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 207 (02) :541-547
[8]   Elevated expression of S100P, CAPL and MAGE 3 in doxorubicin-resistant cell lines: comparison of mRNA differential display reverse transcription polymerase chain reaction and subtractive suppressive hybridization for the analysis of differential gene expression [J].
Bertram, J ;
Palfner, K ;
Hiddemann, W ;
Kneba, M .
ANTI-CANCER DRUGS, 1998, 9 (04) :311-317
[9]  
Borsellino N, 1999, CANCER, V85, P134, DOI 10.1002/(SICI)1097-0142(19990101)85:1<134::AID-CNCR19>3.3.CO
[10]  
2-3