Macrophage Inhibitory Cytokine 1: A New Prognostic Marker in Prostate Cancer

被引:130
作者
Brown, David A. [2 ,3 ]
Lindmark, Fredrik [4 ]
Stattin, Par [5 ]
Balter, Katarina [1 ]
Adami, Hans-Olov [1 ,6 ]
Zheng, Sigun L. [7 ]
Xu, Jianfeng [7 ]
Isaacs, William B. [8 ]
Gronberg, Henrik [1 ]
Breit, Samuel N. [2 ,3 ]
Wiklund, Fredrik E. [1 ]
机构
[1] Karolinska Inst, Dept Med Epidemiol & Biostat, SE-17177 Stockholm, Sweden
[2] St Vincents Hosp, Ctr Appl Med Res, Sydney, NSW 2010, Australia
[3] Univ New S Wales, Sydney, NSW, Australia
[4] Umea Univ, Dept Radiat Sci, Umea, Sweden
[5] Umea Univ, Dept Surg & Preoperat Sci, Umea, Sweden
[6] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[7] Wake Forest Univ, Ctr Human Genom, Winston Salem, NC 27109 USA
[8] Johns Hopkins Univ, Dept Urol, Baltimore, MD USA
基金
英国医学研究理事会;
关键词
GROWTH-FACTOR-BETA; DISEASE RECURRENCE; ANTIGEN; CELLS; MIC-1; EXPRESSION; PROPEPTIDE; P53;
D O I
10.1158/1078-0432.CCR-08-3126
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: High serum levels of macrophage inhibitory cytokine 1 (MIC-1) are strongly associated with metastatic prostate cancer, suggesting MIC-1 is a biomarker for prostate cancer prognosis. Experimental Design: We conducted a prospective cohort study of 1,442 Swedish men with a pathologically verified diagnosis of prostate cancer between 2001 and 2003. Blood was drawn either pretreatment (n = 431) or posttreatment (n = 1,011) and cases were followed for a mean time of 4.9 years (range, 0.1-6.8 years). Results: MIC-1 serum levels independently predicted poor cancer-specific survival with an almost 3-fold higher cancer death rate in patients with serum levels in the highest quartile compared with men with serum levels in the lowest quartile (adjusted hazard ratio, 2.98; 95% confidence interval, 1.82-4.68). Pretreatment MIC-1 levels revealed an even stronger association with disease outcome with an 8-fold higher death rate in the highest compared with the lowest category (adjusted hazard ratio, 7.98; 95% confidence interval, 1.73-36.86). Among patients considered to have localized disease, MIC-1 significantly increased the discriminative capacity between indolent and lethal prostate cancer compared with the established prognostic markers clinical stage, pathologic grade, and prostate-specific antigen level (P = 0.016). A sequence variant in the MIC-1 gene was associated with decreased MIC-1 serum levels (P = 0.002) and decreased prostate cancer mortality (P = 0.003), suggesting a causative role of MIC-1 in prostate cancer prognosis. Conclusions: Serum MIC-1 concentration is a novel biomarker capable of predicting prostate cancer prognosis. (Clin Cancer Res 2009;15(21):6658-64)
引用
收藏
页码:6658 / 6664
页数:7
相关论文
共 35 条
[11]   Antibody-based approach to high-volume genotyping for MIC-1 polymorphism [J].
Brown, DA ;
Bauskin, AR ;
Fairlie, WD ;
Smith, MD ;
Liu, T ;
Xu, N ;
Breit, SN .
BIOTECHNIQUES, 2002, 33 (01) :118-+
[12]  
Demers Laurence M., 2000, Cancer, V88, P2919, DOI 10.1002/1097-0142(20000615)88:12+<2919::AID-CNCR7>3.0.CO
[13]  
2-Z
[14]   Aminoterminal propeptide of type I collagen and bone alkaline phosphatase in the study of bone metastases associated with prostatic carcinoma [J].
Díaz-Martín, MA ;
Traba, ML ;
de la Piedra, C ;
Guerrero, R ;
Méndez-Dávila, C ;
de la Peña, EG .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1999, 59 (02) :125-132
[15]   Reliability of death certificates in prostate cancer patients [J].
Fall, Katja ;
Stromberg, Fredrik ;
Rosell, Johan ;
Andren, Ove ;
Varenhorst, Eberhard .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 2008, 42 (04) :352-357
[16]   Prostate-specific antigen levels as a predictor of lethal prostate cancer [J].
Fall, Katja ;
Garmo, Hans ;
Andren, Ove ;
Bill-Axelson, Anna ;
Adolfsson, Jan ;
Adami, Hans-Olov ;
Johansson, Jan-Erik ;
Holmberg, Lars .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (07) :526-532
[17]   The transforming growth factor-β family members bone morphogenetic protein-2 and macrophage inhibitory cytokine-1 as mediators of the antiangiogenic activity of N-(4-hydroxyphenyl) retinamide [J].
Ferrari, N ;
Pfeffer, U ;
Dell'Eva, R ;
Ambrosini, C ;
Noonan, DM ;
Albini, A .
CLINICAL CANCER RESEARCH, 2005, 11 (12) :4610-4619
[18]   A CLASS OF K-SAMPLE TESTS FOR COMPARING THE CUMULATIVE INCIDENCE OF A COMPETING RISK [J].
GRAY, RJ .
ANNALS OF STATISTICS, 1988, 16 (03) :1141-1154
[19]   A METHOD OF COMPARING THE AREAS UNDER RECEIVER OPERATING CHARACTERISTIC CURVES DERIVED FROM THE SAME CASES [J].
HANLEY, JA ;
MCNEIL, BJ .
RADIOLOGY, 1983, 148 (03) :839-843
[20]   Natural history of early, localized prostate cancer [J].
Johansson, JE ;
Andrén, O ;
Andersson, SO ;
Dickman, PW ;
Holmberg, L ;
Magnuson, A ;
Adami, HO .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (22) :2713-2719